Introduction
Verrucaria Schrad. is one of the most difficult genera among lichens. Relatively simple morphology combined with plasticity in response to environmental conditions make delimitation of the species challenging (Orange & Chhetri Reference Orange and Chhetri2022). Over 900 species have been described in the genus, but most species are considered synonyms or their taxonomic status is uncertain (Pykälä et al. Reference Pykälä, Launis and Myllys2018). The number of currently accepted species of Verrucaria varies from 200 (Orange Reference Orange2013a) to 500–600 (Breuss & Berger Reference Breuss and Berger2010). Gueidan et al. (Reference Gueidan, Savić, Thüs, Roux, Keller, Tibell, Prieto, Heiðmarsson, Breuss and Orange2009) showed that Verrucaria is restricted to its type, V. rupestris Schrad., and the remaining species are not related. However, the phylogenetic position and generic affiliation of most species are still unknown.
During the 1800s and the first half of the 1900s, a significant number of new Verrucaria species were described from Europe (see the monographs of Zschacke (Reference Zschacke and Zahlbruckner1934) and Servít (Reference Servít1954)). Despite this, recent studies suggest that the species richness in the genus is underestimated in Europe, mainly because several groups are poorly collected and understudied due to their small and inconspicuous habit (e.g. Orange Reference Orange2004, Reference Orange2013b, Reference Orange2014, Reference Orange2020; Breuss & Berger Reference Breuss and Berger2012; Thüs et al. Reference Thüs, Orange, Gueidan, Pykälä, Ruberti, Lo Schiavo and Nascimbene2015, Reference Thüs, Killmann, Leh and Fischer2018; Gasparyan & Aptroot Reference Gasparyan and Aptroot2016; Pykälä et al. Reference Pykälä, Launis and Myllys2017a, Reference Pykälä, Launis and Myllysb, Reference Pykälä, Launis and Myllys2018, Reference Pykälä, Launis and Myllys2019, Reference Pykälä, Kantelinen and Myllys2020).
Species with a thin green or brown thallus, rather small perithecia and a usually thin involucrellum reaching the exciple base level form an extremely difficult morphogroup. Previous studies have shown that such species occur widely among Verrucariaceae (Orange Reference Orange2013b; Pykälä et al. Reference Pykälä, Launis and Myllys2018, Reference Pykälä, Launis and Myllys2019; Thüs et al. Reference Thüs, Killmann, Leh and Fischer2018). Here, we study the taxonomy of seven species belonging to this morphogroup. Despite long-lasting efforts to find names for these species, such attempts have failed. Altogether, type material of 434 Verrucaria species has been studied. Thus, we describe them here as new based on morphological and molecular characters.
Material and Methods
Taxon sampling
This study is based on material collected by the first author during the years 2003–2021. The sampling was most extensive on calcareous rocks in Southern Finland (over 50% of all calcareous rock outcrops and lime quarries studied) (Pykälä et al. Reference Pykälä, Launis and Myllys2017a, Reference Pykälä, Launis and Myllysb). Sampling of siliceous rocks has been far less intensive. Finnish bedrock is mainly acid, and siliceous rocks are frequent. Some sampling has also been made on serpentine rocks (mainly during 2020–2021), which are rare in Finland, most often occurring in eastern and northern parts of the country. Type material of morphologically similar Verrucaria species from herbaria B, H, H-NYL, M, PRM, S, UPS and VER was studied for comparison. This includes specimens with small perithecia (less than 0.3 mm), a thin brown or green thallus, an involucrellum mainly reaching the exciple base level and small to medium sized spores (10–25 × 5–12 μm).
Morphology
Perithecia and thalli were hand-sectioned with razor blades. The sections were examined and measured in tap water. Asci and ascospores were also studied in squash preparations of perithecia mounted in water. Sections and squash preparations of old herbarium specimens were studied using 10% potassium hydroxide (KOH). Additionally, involucrellum characters and exciple colour and diameter were examined by cutting perithecia into two pieces and studying the pieces using a stereomicroscope. The range of spore size is indicated as arithmetic mean and standard deviation (x̄ ± SD) with minimum and maximum values given in parentheses, and n = the number of measurements made. The size of the perithecia (diam.) is given in surface view. The colour of the wall of the exciple was assessed from the basal parts.
Specimens were photographed with a Nikon Z50 camera attached to Leica Z16 and Leica DM 2500 microscopes. Layered images were taken manually from 6 to 8 points and stacked by using Corel PaintShop Pro 2023 software.
DNA extraction and sequencing
Total genomic DNA was extracted from the perithecia (1–3) of 1–15-year-old herbarium specimens. We used two different techniques for extraction and sequencing. Most Finnish samples were sequenced during the research project ‘Finnish Barcode of Life’ between 2012–2021 (FinBOL; https://finbol.org/). The two Norwegian specimens were obtained from the Norwegian lichen DNA barcoding project (OLICH).
DNA samples were placed in 96-well microplates and sent to the Canadian Centre for DNA Barcoding (CCDB). CCDB's standard protocols (documentation available at http://ccdb.ca/resources) were used for extraction, PCR and sequencing. Primers ITS1 and ITS4 (White et al. Reference White, Bruns, Lee, Taylor, Innis, Gelfand, Sninsky and White1990) were used both for PCR and sequencing of the nuclear ribosomal ITS region. For the Norwegian specimens, the primers ITS5 and ITS4 (White et al. Reference White, Bruns, Lee, Taylor, Innis, Gelfand, Sninsky and White1990) were used for PCR, and ITS1 and ITS4 for sequencing. The barcode sequences, their trace files, along with all relevant collection data and images of the voucher specimens were uploaded to the Barcode of Life Data Systems (BOLD; https://www.boldsystems.org) database.
DNA of the 11 specimens (Pykälä 27107, 29774, 29883, 31875, 36440, 54604, 56270, 57469, 58042, 58317, 59214) was extracted using the DNeasy® Blood & Tissue Kit by Qiagen, following the protocol described in Myllys et al. (Reference Myllys, Velmala, Holien, Halonen, Wang and Goward2011). PCR reactions were prepared using PuReTaq Ready-To-Go PCR beads (GE Healthcare). The 25 μl reaction volume contained 19 μl of dH2O, 0.4 μM of each primer and 4 μl of extracted DNA. PCR was run under the following conditions: initial denaturation for 5 min at 95 °C followed by five cycles of 30 s at 95 °C (denaturation), 30 s at 58 °C (annealing), and 1 min at 72 °C (extension); in the remaining 35 cycles, the annealing temperature was decreased to 56 °C; the PCR schedule ended with a final extension for 7 min at 72 °C. PCR products were purified and sequenced by Macrogen Inc. (Amsterdam, The Netherlands; www.macrogen.com) or, alternatively, cleaned with ExoSAP (Affymetrix, Santa Clara, California, USA) and sequenced by FIMM Genomics (https://www.helsinki.fi/en/infrastructures/genome-analysis/infrastructures/fimm-genomics). The primers ITS1F (Gardes & Bruns Reference Gardes and Bruns1993) and ITS4 (White et al. Reference White, Bruns, Lee, Taylor, Innis, Gelfand, Sninsky and White1990) were used both for PCR amplification and sequencing of the ITS regions.
Phylogenetic analyses
BLAST (Altschul et al. Reference Altschul, Gish, Miller, Myers and Lipman1990) was used to search for the most similar ITS sequences available on GenBank. First, all sequences exceeding 97% similarity were selected. Seven GenBank sequences for V. linkolae and one V. hunsrueckensis Thüs et al. sequence for V. vainioi met this criterion. Second, if sequences exceeding this threshold were not found, one sequence each of the two most similar species were included in the phylogeny. These included ITS sequences of V. hunsrueckensis, V. hydrophila Orange, V. nodosa Orange (from type material), V. phloeophila Breuss, V. placida Orange, V. rosula Orange and Verrucaria spp. The similarities of these sequences varied from 96.3% to 92.4%. Sequences obtained from the holotype specimens of V. hunsrueckensis, V. hydrophila and V. rosula were included for comparison. In total, 21 ITS sequences representing seven Verrucaria species and eight unidentified Verrucaria specimens were selected and downloaded from GenBank. However, unidentified specimens from soil samples were not included in the analyses. Verrucaria macrostoma Dufour ex DC. and V. nigrescens Pers. were chosen as outgroups based on earlier results by Orange (Reference Orange2013a) and Thüs et al. (Reference Thüs, Killmann, Leh and Fischer2018) on the systematic position of the selected Verrucaria species. A total of 73 ITS sequences were aligned with MUSCLE v. 3.8.31 (Edgar Reference Edgar2004) using EMBL-EBI's freely available web service (http://www.ebi.ac.uk/Tools/msa/muscle/). The aligned data set was subjected to maximum likelihood analysis (ML). The analysis was performed with RAxML v. 8.1.15 (Stamatakis Reference Stamatakis2014) on the CSC – IT Center for Science server ((http://www.csc.fi). The ITS region was divided into three partitions: ITS1, 5.8S and ITS2. These partitions were analyzed under the universal GTR-GAMMA model. Node support was estimated with 1000 bootstrap replications using the rapid bootstrap algorithm. Branches with bootstrap values ≥ 70% were considered strongly supported.
Results and Discussion
We generated 50 new ITS sequences for this study (Table 1). In the ITS phylogeny, seven new lineages were observed (Fig. 1). These lineages, when represented by multiple samples, received high support values (86–100%). Since we did not find any existing names for these clades, we describe them as new species (see ‘The Species’).
Table 1. Verrucaria specimens with voucher information and GenBank Accession numbers, used in the phylogenetic analyses. New ITS sequences are in bold.
Figure 1. Phylogenetic relationships of the studied Verrucaria species based on a maximum likelihood (ML) analysis of the ITS data set. Maximum likelihood bootstrap values > 50% are shown at nodes. Thickened lines indicate bootstrap values > 70%. New species described in this study are indicated with shadowed boxes and holotype specimens are shown in bold. GenBank Accession numbers for sequences downloaded from GenBank and collection numbers for the specimens sequenced for this study are shown after the taxon names. In colour online.
Verrucaria juumaensis sp. nov. (represented by five specimens in our study) and V. hakulinenii sp. nov. (three specimens) form a strongly supported (98% bootstrap support) sister group. Together they cluster with V. hydrophila, V. placida and V. phloeophila with high confidence (100%). A single specimen of V. lohjaensis sp. nov. groups with one V. rosula specimen collected in China (MN103180) and one Verrucaria specimen collected from the Czech Republic (OL457961) with moderately low support (62%). However, the Chinese collection is most probably a misidentification since the ITS sequence obtained from the holotype of V. rosula does not group with this specimen. It is noteworthy that our 14 V. linkolae specimens form a strongly supported (100%) group with two V. hegetschweileri Körb., nom. illeg. non (Naegeli ex Hepp) Garov. specimens, three Verrucaria sp. specimens from the Czech Republic (OK332900, OK332901, OL396617), one Verrucaria sp. specimen from Germany (MG242447) and one Verrucaria sp. specimen collected in Great Britain (FJ664851). As discussed in the taxonomy section below, we suspect that all these specimens actually represent our new species V. linkolae. The species forms a moderately strongly supported group (76%) with V. oulankajokiensis sp. nov. (two specimens), V. vainioi sp. nov. (six specimens), V. norrlinii sp. nov. (14 specimens), V. hunsrueckensis, V. nodosa, five Verrucaria sp. specimens collected in Finland (28977, 35945, 47727, 55769, 59214) by the first author, and two Verrucaria sp. specimens collected in Scotland (FJ667941) and Iceland (FJ664859) by Alan Orange. The last mentioned specimen forms a strongly supported group (90%) with V. nodosa and our new species, V. vainioi forms a strongly supported group (90%) with V. hunsrueckensis and the collection from Scotland, while V. norrlinii and V. oulankajokiensis group with V. nodosa and specimens collected from Finland and Iceland with moderately strong support (75%).
According to the phylogeny, the new species V. juumaensis and V. hakulinenii belong to an informal group referred to as the Verrucaria hydrophila group (see Pykälä et al. Reference Pykälä, Launis and Myllys2018; Thüs et al. Reference Thüs, Killmann, Leh and Fischer2018; Orange & Chhetri Reference Orange and Chhetri2022). In the multi-locus phylogeny of Thüs et al. (Reference Thüs, Muggia, Pérez-Ortega, Favero-Longo, Joneson, O'Brien, Nelsen, Duque-Thüs, Grube and Friedl2011), the V. hydrophila group is placed as a sister to Trimmatothele Norman ex Zahbr. Furthermore, our results suggest that V. linkolae, V. norrlinii, V. oulankajokiensis and V. vainioi are closely related to the V. nodosa/hunsrueckensis group (see Thüs et al. Reference Thüs, Killmann, Leh and Fischer2018).
Generally, Verrucaria species are considered to be either corticolous or epilithic (e.g. Lendemer & Breuss Reference Lendemer and Breuss2009). However, our studies show that V. linkolae and V. norrlinii (this study), and V. hydrophila (Pykälä et al. Reference Pykälä, Launis and Myllys2018) may occur on both substrata. All three of these species are chiefly epilithic, but are also rarely found on bark.
The Species
All cited specimens of the new species are deposited in H.
Verrucaria hakulinenii Pykälä & Myllys sp. nov.
MycoBank No.: MB 852433
Differing from Verrucaria tenebrosa Pykälä et al. by the paler and larger thallus and more immersed perithecia.
Type: Finland, Varsinais-Suomi, Pohja, Kuovila, 400 m SE of Kalkkuuninmäki, Picea abies-dominated OMT-forest, abandoned lime quarry, on E-facing wall, 46 m a.s.l., 60°08ʹN, 23°24ʹE, 12 October 2006, J. Pykälä 29774 (H9203803—holotype). GenBank Accession no.: PP337728.
Figure 2. A, Verrucaria hakulinenii (holotype). B, V. juumaensis (holotype). C, V. linkolae (holotype). D, V. lohjaensis (holotype). E, V. norrlinii (holotype). F, V. oulankajokiensis (holotype). G, V. vainioi (holotype). Scales = 0.5 mm. In colour online.
Figure 3. Sections of perithecia. A, Verrucaria hakulinenii (holotype). B, V. juumaensis (holotype). C, V. linkolae (holotype). D, V. lohjaensis (holotype). E, V. norrlinii (holotype). F, V. oulankajokiensis (holotype). G, V. vainioi (holotype). Scales = 0.1 mm. In colour online.
Thallus continuous, rimose to cracked-areolate, pale green, medium green to medium brownish green, after storage pale brownish grey, c. 0.05–0.1 mm thick, areoles 0.2–0.8 mm, algal cells c. 6–10 × 5–8 μm, medulla not differentiated, algal cells distributed throughout, cortex not clearly differentiated, c. 10–30 μm thick, cortical cells pale or brown. Prothallus not seen or brown, non-fimbriate.
Perithecia 0.13–0.26 mm diam., 1/2–3/4-immersed, not leaving pits, often with a thin thalline cover except at the apex, c. 110–200 perithecia per cm2. Ostiole tiny, pale to dark, plane or depressed, c. 10–30 μm wide. Involucrellum to the exciple base, c. 25–70 μm thick, appressed to the exciple or slightly diverging from it near the base. Exciple c. 0.15–0.24 mm diam, wall pale to medium brown, c. 22–25 μm thick. Periphyses c. 17–25 × 1–2 μm, branching. Asci 8-spored, c. 45–65 × 20–23 μm. Ascospores (16.8–)18.4–20.2–21.8(–24.7) × (6.5–)7.6–8.6–9.6(–11.1) μm (n = 98).
Etymology
Named after Rainar Hakulinen (1918–1991), an important link in the chain of Finnish lichenologists (see Ahti Reference Ahti1993).
Ecology and distribution
Only two localities are known: one in SW Finland and one in NW Finland, c. 1000 km apart. In inland SW Finland, the species grows on an E-facing wall of an abandoned lime quarry. In NW Finland, the species is known only from a dolomite rock outcrop on a river shore on a subarctic fell.
Notes
The two populations of V. hakulinenii have minor morphological differences. However, due to the high sequence similarity of the ITS regions (99%) they are included here in the same species. Verrucaria hakulinenii differs in several characteristics from the other species treated in this study. Of the species belonging to the V. hydrophila group, it mostly resembles V. tenebrosa Pykälä et al. which, however, usually has a darker, often brown, more weakly developed thallus and less immersed and more sparsely occurring perithecia (Pykälä et al. Reference Pykälä, Launis and Myllys2018). Verrucaria hakulinenii also shares some morphological similarities with other, less closely related species. Verrucaria tallbackaensis Pykälä et al. has less immersed perithecia, often pale ostioles with projecting papillae and smaller spores (Pykälä et al. Reference Pykälä, Launis and Myllys2019). The description of V. floerkeana Dalla Torre & Sarntheim by Breuss & Berger (Reference Breuss and Berger2010) is rather similar to the description of V. hakulinenii. Based on Breuss & Berger, V. floerkeana has a larger exciple (0.2–0.3 mm), smaller spores (15–20(–22) × 6–9 μm), a thinner involucrellum (20–30 μm thick) and thicker periphyses (3 μm thick). The identity of V. floerkeana is not clear (several specimens cited in the protologue), and the species is in need of lectotypification.
Additional specimens examined
Finland: Enontekiön Lappi: Enontekiö, Porojärvet, Toskalharji, Toskaljärvi N, fell, brook, W-shore, dolomite rock outcrop, on N-slope, 710 m a.s.l., 69°11ʹN, 21°26ʹE, 2011, J. Pykälä 43448, 43451.
Verrucaria juumaensis Pykälä & Myllys sp. nov.
MycoBank No.: MB 852434
Differing from Verrucaria hakulinenii sp. nov. by a more reduced thallus, less immersed perithecia, narrower spores and the occurrence of goniocyst-like units.
Type: Finland, Koillismaa, Kuusamo, Juuma, Oulanka National Park, Hautaniitynvuoma, gorge, dolomite rock outcrop, on high NE-facing wall, 190 m a.s.l., 66°15ʹN, 29°22ʹE, 21 August 2011, J. Pykälä 44700 (H9204984—holotype). GenBank Accession no.: PP337732.
Thallus pale green, brownish green, medium greenish brown, dark brown, in one specimen with some grey pruina, fleck-like to rarely rimose, usually tiny flecks, c. 5–100 μm thick, partly consisting of goniocyst-like units, c. 40–80 μm, algal cells 5–8 μm, cortex pale brown to dark brown, often weakly differentiated. Prothallus absent or weakly developed, dark brown, fimbriate.
Perithecia 0.18–0.27 mm diam., 1/4–1/2-immersed to superficial, c. 40–160 perithecia per cm2. Ostiole inconspicuous, tiny, dark, rarely pale, plane to depressed, c. 10–30 μm wide. Involucrellum to the exciple base or more rarely enveloping the exciple, c. (20–)30–40 μm thick. Exciple 0.14–0.20 mm, wall pale to dark brown. Periphyses c. 15–20 × 2 μm. Asci 8-spored, c. 56–90 × 13–15 μm. Ascospores (15.5–)18.0–20.5–22.7(–24.9) × (5.8–)6.7–7.3–7.8(–8.5) μm (n = 66).
Etymology
The specific epithet refers to the village of Juuma in Kuusamo from where two specimens, including the type, originate.
Ecology and distribution
Verrucaria juumaensis has been collected from dolomite and serpentine rocks, both on rock outcrops and on pebbles. All the localities are in Eastern Finland, in the biogeographical provinces of Kainuu and Koillismaa. The species may have been overlooked due to its small size and morphological similarity with several species of Verrucaria, but it is also apparently rare in Finland. It may belong to the north-eastern element that can be found in Finland only in the eastern region of the country. An unidentified sequence from a soil sample from Canada (KC 965589) (Timling et al. Reference Timling, Walker, Nusbaum, Lennon and Taylor2014) differs only in two bases in the ITS regions, and most probably belongs to V. juumaensis.
Notes
This species differs from its sister species V. hakulinenii by a more reduced thallus, less immersed perithecia and narrower spores. Verrucaria floerkeana has a paler and thicker thallus lacking goniocyst-like units, a larger exciple and thinner involucrellum (see the description in Breuss & Berger (Reference Breuss and Berger2010)). Verrucaria oulankajokiensis has a pale exciple wall, a rimose to areolate thallus and smaller perithecia. Verrucaria juumaensis is difficult to separate from several other unrelated species of Verrucaria. Verrucaria juankoskiensis Pykälä & Myllys has a thicker involucrellum and slightly narrower spores (Pykälä et al. Reference Pykälä, Launis and Myllys2019). Verrucaria kalenskyi Servít and V. raesaenenii Pykälä & Myllys, both members of the V. praetermissa (Trevis.) Anzi group, have smaller spores, slightly smaller perithecia and thalli that lack goniocyst-like units (Pykälä et al. Reference Pykälä, Launis and Myllys2019). In V. kalenskyi, the prothallus is absent. Verrucaria lapidicola Orange from the same group has smaller perithecia (in the Finnish material up to 0.22 mm, but usually 0.11–0.17 mm) (Pykälä Reference Pykälä2023). Verrucaria infumata Nyl. may be superficially a rather similar species but it has broader spores (c. 7–10 μm wide). Specimens with the involucrellum enveloping the exciple may be confused with V. xyloxena Norman. Verrucaria xyloxena lacks an involucrellum, ostioles often have pale, projecting papillae and the spores are smaller.
Additional specimens examined
Finland: Koillismaa: Salla, Oulanka National Park, Pikkuköngäs, shore of River Oulankajoki, high cliff, calciferous (dolomite) schistose rock outcrop, on overhanging SE-facing wall, 180 m a.s.l., 66°25ʹN, 29°09ʹE, 2010, J. Pykälä 39204; Kuusamo, Juuma, Myllyniemi SE, steep N-slope, dolomite rock outcrop on shore of Lake Yli-Juumajärvi, on 60 cm high N-facing wall, on dolomite pebbles, 225 m a.s.l., 66°15ʹN, 29°22ʹE, 2021, J. Pykälä 58317. Kainuu: Paltamo, Mieslahti, Mineraali, Pinus sylvestris-dominated, slightly paludified heath forest, ECT site type, on serpentine boulder, on N-facing wall, 158 m a.s.l., 64°19ʹN, 28°02ʹE, 2020, J. Pykälä 54852; Paltamo, Mieslahti, Heinimäki, calcareous rock outcrop, E-facing wall, crevice, on pebble, 143 m a.s.l., 64°20ʹN, 28°02ʹE, 2020, J. Pykälä 55391.
Verrucaria linkolae Pykälä & Myllys sp. nov.
MycoBank No.: MB 852435
Differing from other European Verrucaria species with a brown thallus and goniocyst-like units by the smaller, occasionally 1-septate, spores.
Type: Finland, Varsinais-Suomi, Lohja, Paloniemi, S of Paloniemi, house ruins, on bricks, half-shady habitat, 43 m a.s.l., 60°16ʹN, 24°00ʹE, 18 July 2005, J. Pykälä 27347 (H9204043—holotype). GenBank Accession no.: PP337737.
Thallus pale greyish brown, greenish brown to usually dark brown, fleck-like, granular or continuous, sometimes tiny flecks, goniocyst-like units often present, c. 25–50 μm, algal cells c. (4–)5–7(–10) μm, cortex thin, cortical cells hyaline to brown, c. 3–5 μm. Prothallus absent or brown fimbriate.
Perithecia 0.11–0.19 mm diam., 1/4–1/2(–3/4)-immersed, c. 100–330 perithecia per cm2. Ostiole inconspicuous, tiny, dark, plane, depressed or projecting papillae, c.10–30 μm wide. Involucrellum to the exciple base level, c. 15–30(–40) μm thick, rarely thickening to the base to c. 40–50 μm thick, appressed to the exciple or slightly diverging. Exciple 0.10–0.16 mm, wall pale to medium brown, 19–23 μm thick. Periphyses c. 10–18 × (1–)2–2.5(–3) μm. Asci 8-spored, c. 37–68 × 12–17 μm. Ascospores aseptate, in few specimens occasionally/predominantly 1-septate, (11.4–)12.6–13.9–15.2(–17.4) × (4.4–)5.0–5.7–6.4(–7.6) μm (n = 236).
Etymology
Named after Kaarlo Linkola (1888–1942), one of Finland's most eminent botanists, nature conservationists and lichenologists.
Ecology and distribution
Verrucaria linkolae seems to be common in Southern and Central Finland. It is common on siliceous rocks but may be rare on calcareous and serpentine rocks. It prefers pebbles and stones on the ground and also grows on bricks. Pebbles and stones can occur in herb-rich and heath forests as well as on road verges and lime quarry spoils. One locality is from an overhanging wall in a lime quarry. The species may prefer half-shady and shady habitats. However, some localities are rather sun-exposed. Most localities are rather dry but the species has also been collected on periodically wet stones by a brooklet. The species was once collected on exposed roots of Betula on a road bank (calcareous soil).
In GenBank, the specimens which are likely to belong to V. linkolae (over 98% similarity in the ITS regions; see below) are from the Czech Republic (OK332900, OK332901, OK333039, OK333040, OL396617), the United Kingdom (FJ664851) and Germany (MG242447).
Notes
Seven GenBank ITS sequences have over 98% similarity with those of V. linkolae and are likely to represent this species. The specimens have been previously identified as Verrucaria sp. and with the illegitimate name V. hegetschweileri Körb. ex Nyl. (two epiphytic specimens). Verrucaria linkolae fits rather well with the description of V. hegetschweileri (Körb. ex Nyl. (illeg.) non (Naegeli ex Hepp) Garov.) in Breuss (Reference Breuss1998) and Lendemer & Breuss (Reference Lendemer and Breuss2009), but the latter differs in the inclusion of specimens without an involucrellum, while all sequenced specimens seen so far from Finland do have an involucrellum. We considered V. linkolae as a replacement name for the illegitimate V. hegetschweileri Körb. ex Nyl. and studied the material used for its description (Baar pr. Zug ad fagorum radices, Hegetschweiler (H-NYL 3316!)), but based on our inspection, the morphology does not correspond to that of V. linkolae. The specimen has a grey to pale brown thallus, an involucrellum at the exciple base level (not enveloping the exciple) and larger spores (16–21 × 7–8 μm) compared to V. linkolae.
Most specimens of V. linkolae have only aseptate spores but in a small number of specimens, 1-septate spores are frequent. Verrucaria linkolae is difficult to separate from several species of Verrucaria with small perithecia, rather small spores and a predominantly brown thallus. Species with thalli consisting of goniocyst-like units, V. hunsrueckensis, V. lapidicola, V. norrlinii and V. umbrinula Nyl., may be the most similar. These species usually have larger spores but some specimens have a spore size similar to V. linkolae. Verrucaria norrlinii has, on average, more immersed perithecia, which are less densely spaced and slightly larger. Verrucaria umbrinula has slightly larger perithecia (up to 0.22 mm) and a thicker thallus. Verrucaria lapidicola is restricted to calcareous rocks, the perithecia tend to be slightly larger (up to 0.22 mm) and 1-septate spores have not been reported (Pykälä Reference Pykälä2023). Verrucaria hunsrueckensis is otherwise morphologically similar but has slightly larger spores (x̄ 16.8 × 6.6 μm vs 13.9 × 5.7 μm in the Finnish specimens in this study).
Verrucaria memnonia auct. may be a similar species based on the description in Breuss & Berger (Reference Breuss and Berger2010). We have examined the three syntypes of V. memnonia (Flot.) Arnold: Ad saxa granitica (rarius schistose) in sylvis umbrosis vallis Hirschbergensis Silesiae, Körber, Körber, Lich. Sel. Germ. 173 (M-01565311!); Sattler prope Hirsch bergam Silesiae 1854 Körber (VER!); Räuberberg im Sattler bei Hirschberg 3.6.1840 Körber (UPS!). However, none of these is identifiable to any lichen genus (putative perithecia are overmature, and it is uncertain whether the structures are even perithecia). Thus, unless better developed syntypes are found, V. memnonia auct. (sensu Breuss & Berger Reference Breuss and Berger2010) as well as V. memnonia (Flot.) Arnold should be treated as a species of unknown identity.
Additional specimens examined
Finland: Varsinais-Suomi: Lohja, Marttila, Savilahdensalmi, Seppälänsaari road, steep road bank, on exposed roots of Betula, 37 m a.s.l., 60°14ʹN, 23°51ʹE, 2005, J. Pykälä 27107; Nummi-Pusula, Hyönölä, Remo, clear-cut forest, abandoned lime quarry, on overhanging S-facing wall, 70 m a.s.l., 60°28ʹN, 23°57ʹE, 2006, J. Pykälä 29400; Salo (Kisko), Haapaniemi, Hauksuonlahti, clear-cut herb-rich forest, heap of calcareous stones of lime quarry spoil, on calcareous stones, 50 m a.s.l., 60°12ʹN, 23°30ʹE, 2010, J. Pykälä 37711; Lohja, Vappula, Haukkavuori 200 m NW, road verge, on siliceous pebbles, 55 m a.s.l., 60°13ʹN, 24°00ʹE, 2015, J. Pykälä 48795; Lohja, Maksjoki, former trotting track, young Pinus sylvestris forest, road verge, soil heap, on siliceous pebbles, 65 m a.s.l., 60°13ʹN, 24°02ʹE, 2019, J. Pykälä 52420; Lohja, Koikkala, Nälköönlampi N, former summer cottage, stony heath forest, on siliceous pebbles, 86 m a.s.l., 60°18ʹN, 24°12ʹE, 2019, J. Pykälä 52423; Karkkila, Haavisto, Koirakallio 400 m NW, brooklet, Alnus incana-dominated wet herb-rich forest, on siliceous stones, 76 m a.s.l., 60°29ʹN, 24°20ʹE, 2020, J. Pykälä 54723. Pohjois-Savo: Kuopio (Nilsiä), Nilsiä, Iso-Loutteinen E, abandoned gravel pit, field, young mixed forest, on bricks, 150 m a.s.l., 63°13ʹN, 28°02ʹE, 2020, J. Pykälä 55547. Pohjois-Karjala: Kuopio (Juankoski), Säyneiskylä, Lehtola, 150 m NE, clear-cut forest, top of serpentine boulder, on pebbles, 144 m a.s.l., 63°07ʹN, 28°39ʹE, 2019, J. Pykälä 54003. Kainuu: Paltamo, Melalahti, Melalahdentie, road bank, on siliceous pebbles, 157 m a.s.l., 64°24ʹN, 27°40ʹE, 2020, J. Pykälä 55040; Sotkamo, Jormaskylä, Raatteikonpuro E, Pinus sylvestris/Picea abies-dominated heath forest, EVT site type, on serpentine pebble, 215 m a.s.l., 63°57ʹN, 28°08ʹE, 2020, J. Pykälä 55267. Koillismaa: Kuusamo, Oulanka national park, Jäkälävuoma, gorge, steep SE-slope, sparse herb-rich forest, on pebbles, 215 m a.s.l., 66°15ʹN, 29°26ʹE, 2009, J. Pykälä 36440.
Verrucaria lohjaensis Pykälä & Myllys sp. nov.
MycoBank No.: MB 852436
Differing from other species of the Verrucaria hydrophila group by the small areolate thallus mosaically dark brown and white, and by the more conspicuous ostioles.
Type: Finland, Varsinais-Suomi, Lohja, Lohja, Pitkäniemi industrial area, calcareous rock outcrop, on SW-slope, 40 m a.s.l., 60°15ʹN, 24°03ʹE, 23 July 2021, J. Pykälä 58042 (H9242535—holotype). GenBank Accession no.: PP337750.
Thallus mosaically dark brown and white, areolate, c. 0.1–0.15 mm thick, sterile areoles 0.15–0.3 mm, algal cells c. 4–8 μm, cortex thin, cortical cells hyaline to brown. Prothallus not seen.
Perithecia 0.16–0.22 mm diam., 3/4-immersed in thallus, c. 80–160 perithecia per cm2. Ostiole pale, plane, c. 20–50 μm wide. Involucrellum covering half of the exciple or to the exciple base level, c. 30–40 μm thick, appressed to the exciple. Exciple c. 0.18–0.21 mm, wall brown. Periphyses c. 12–20 × 2 μm. Ascospores aseptate, (16.6–)17.7–19.9–22.1(–24.4) × (7.3–)7.5–7.9–8.3(–8.6) μm (n = 14).
Etymology
The species was named after the municipality of Lohja, where the only known collection is from. Lohja is among the hot spots of lichen diversity and red-listed lichens in Finland.
Ecology and distribution
It is known to have been found in only one locality: a sun-exposed calcareous rock outcrop in inland SW Finland.
Notes
The thallus morphology of V. lohjaensis is different from that of the other species treated in this study. However, other morphological characteristics fit in rather well with the other species treated here. Superficially, V. lohjaensis may resemble some species in the Verrucaria nigrescens Pers. complex or in Placopyrenium Breuss.
Verrucaria norrlinii Pykälä & Myllys sp. nov.
MycoBank No.: MB 852437
Differing from Verrucaria linkolae sp. nov. by the usually less densely occurring and less immersed perithecia.
Type: Finland, Kainuu, Kuhmo, Vieksi, Kellojärvi, Näätäniemi, serpentine rock outcrop on shore of Lake Kellojärvi, under overhanging N-facing wall of serpentine boulder, on serpentine pebbles, 163 m a.s.l., 64°14ʹN, 29°01ʹE, 17 August 2020 J. Pykälä 56243 (H9223911—holotype). GenBank Accession no.: PP337761.
Thallus medium brown to dark brown, fleck-like, granular or continuous, more rarely rimose to areolate, in which case the surface is granular, c. 10–250 μm thick, commonly invaded by algae, often composed of goniocyst-like units c. 20–35 μm, algal cells c. 5–8 μm, cortex absent to thin, cortical cells brown. Prothallus absent or brown fimbriate.
Perithecia 0.12–0.23 mm diam., 1/4–3/4-immersed in thallus, c. 60–160 perithecia per cm2. Ostiole inconspicuous, tiny, pale to dark, plane or projecting papillae, 10–30 μm wide. Involucrellum to the exciple base level or rarely enveloping the exciple, c. 15–30 μm thick, rarely 30–50 μm thick, appressed to the exciple or slightly diverging from it. Exciple 0.11–0.21 mm, wall pale to brown, c. 20 μm thick. Periphyses c. 12–20 × 1.5–2.5 μm. Asci 8-spored, c. 40–59 × 15–23 μm. Ascospores aseptate, (10.2–)13.4–15.9–18.4(–25.5) × (4.8–)5.6–6.6–7.5(–10.8) μm (n = 168).
Etymology
Named after J. P. Norrlin (1842–1917), a Finnish plant geographist and lichenologist. Norrlin collected a rather high number of lichens in Finland, which W. Nylander described as new. Many of them are at present accepted species (Pykälä & Lommi Reference Pykälä and Lommi2021).
Ecology and distribution
The species may be rather common in Southern Finland. The most northern localities are in Kittilä and Kuusamo (in the southern part of the northern boreal vegetation zone), but the distribution area may extend further north. Two sequenced specimens are available from Norway. Thus, the species may be widely distributed in the boreal vegetation zone in Fennoscandia.
Habitats of the species are rather variable. It grows on calcareous, siliceous and serpentine rocks, particularly on pebbles. It also often occurs on road banks on pebbles. However, most localities are from calcareous and serpentine rocks. The species may be edaphically relatively demanding and uncommon on siliceous rocks. This is different from V. linkolae, which prefers siliceous rocks. Two collections are from the exposed roots of Alnus (one from A. glutinosa and one from A. incana) on lake shores. It is likely that the species has more epiphytic occurrences, but epilithic populations seem to be predominant. Further studies are needed to establish whether epiphytic occurrences are restricted to shores. Such occurrences on shores are unexpected since epilithic populations are usually found in rather dry habitats.
Notes
The species has a very high variation in the size of its spores which makes identification based on morphology somewhat difficult. Furthermore, five Verrucaria specimens which clustered outside of V. norrlinii (28977, 47727, 35945, 59214, 55769) were morphologically indistinguishable from our new species. Verrucaria norrlinii is also difficult to separate from, for example, V. linkolae and impossible to separate from V. hunsrueckensis (for a description of the latter species see Thüs et al. (Reference Thüs, Killmann, Leh and Fischer2018) and Pykälä (Reference Pykälä2023)), but V. linkolae often has more densely occurring perithecia. Verrucaria linkolae has on average smaller spores, but in some specimens of V. norrlinii the spore size is similar to V. linkolae. Perithecia of V. norrlinii tend to be more immersed in the thallus compared to V. linkolae. Verrucaria mauriza Nyl. (type: [Russia,] Nyland, Hogland, vid Selkäpajanlahti 11.6.1870, M. Brenner (H!, TUR-V!, syntypes)) has more densely distributed perithecia (c. 160–200 perithecia per cm2) and a thicker involucrellum (c. 50–60 μm thick). Verrucaria buellioides Servít (type: Germania, Heidelberg, auf Porphyrfelsen bei Handschuhsheim, Zwackh-Holzhausen, Zwackh, Lich. Exs. 151 (M-0204053!, holotype, UPS!, isotype); An Porphyrfelsen im Tü… bei Handschuhsheim … 151 / 1848 Zwackh (PRM-756818!, isotype)) differs in the more densely occurring perithecia (c. 200 perithecia per cm2). The spore size (c. 16–20 × 7(–9) μm) is also larger than usual in V. norrlinii.
Additional specimens examined
Finland: Varsinais-Suomi: Lohja, Lohja, 100 m S of Hiidensalmi bridge, stony shore of Lake Lohjanjärvi, on exposed thick root of dead Alnus incana, 32 m a.s.l., 60°16ʹN, 24°03ʹE, 2006, J. Pykälä 29883; Lohja, Lohja, Kiviniemi lime quarry, beneath N-facing wall, on boulder, 35 m a.s.l., 60°15ʹN, 24°03ʹE, 2007, J. Pykälä 30542; Lohja, Hermala, Kalkkimäki, 20 m E of Kekla lime quarry, flat calcareous rock outcrop, 65 m a.s.l., 60°13ʹN, 23°51ʹE, 2007, J. Pykälä 31030; Lohja, Piispala, Puntari, Kalvik, shore forest of Lake Lohjanjärvi, on shore, on exposed thick roots of Alnus glutinosa, 32 m a.s.l., 60°11ʹN, 23°52ʹE, 2007, J. Pykälä 31875; Kemiönsaari (Hiittinen), Holma, Långholmen Island, siliceous rock outcrop on shore of the Baltic Sea, gentle W-slope, on narrow vein of calcite, 1 m a.s.l., 59°53ʹN, 22°22ʹE, 2010, J. Pykälä 38854. Pohjois-Karjala: Kuopio (Juankoski), Säyneiskylä, Pajumäki, beneath NE-facing wall of serpentine rock outcrop, on top of uprooted windfall Picea abies, on pebbles, 130 m a.s.l., 63°09ʹN, 28°36ʹE, 2020, J. Pykälä 55480, 55483. Kainuu: Kuhmo, Vieksi, Kellojärvi, Näätäniemi, Junkiniemi 150 m S, young Pinus sylvestris-dominated heath forest, tiny serpentine rock outcrop, on serpentine pebbles, 175 m a.s.l., 64°14ʹN, 29°01ʹE, 2020, J. Pykälä 56259; Kuhmo, Vieksi, Kellojärvi, Perttilä 200 m S, abandoned soapstone quarry, on top of NE-facing wall, 172 m a.s.l., 64°15ʹN, 29°02ʹE, 2020, J. Pykälä 56270; Kuhmo, Vieksi, Kellojärvi, Kivihiekka E, mixed heath forest, VMT site type, serpentine rock outcrop, on W-facing wall, 172 m a.s.l., 64°17ʹN, 29°03ʹE, 2021, J. Pykälä 57469. Koillismaa: Kuusamo, Kurvinen, Pieni Rajakumpu 200 m SE, Pinus sylvestris heath forest, ECT site type, path, on serpentine stones, 245 m a.s.l., 65°35ʹN, 29°43ʹE, 2020, J. Pykälä 55698.—Norway: Sør-Trøndelag: Oppdal, Kongsvoll, S of Kongsvoll Fjeldstue, subalpine sparse Betula pubescens forest, stony path, on pebbles, 960 m a.s.l., 62°17ʹN, 9°36ʹE, 2015, J. Pykälä 48271; Oppdal, Kongsvoll, N-NE of Kongsvoll, main road, road cutting of a schistose rock outcrop, under overhanging wall, on pebbles, 890 m a.s.l., 62°18ʹN, 9°36ʹE, 2015, J. Pykälä 48279.
Verrucaria oulankajokiensis Pykälä & Myllys sp. nov.
MycoBank No.: MB 852438
Differing from V. kalenskyi and V. raesaenenii by perithecia that are often thinly thalline covered, and a thallus that is partly surrounded by dark thalline lines.
Type: Finland, Koillismaa, Salla, Oulanka National Park, Pikkuköngäs, shore of River Oulankajoki, high cliff, calciferous (dolomite) schistose rock outcrop, on SW-facing wall, rather scarce, 178 m a.s.l., 66°25ʹN, 29°09ʹE, 10 August 2009, J. Pykälä 36048 (H9205776—holotype). GenBank Accession no.: PP337765.
Thallus pale brown, medium greenish brown to dark brown, rimose to small areolate, areoles 0.1–0.25 mm, partly surrounded by dark thalline line, c. 20–100 μm thick, algal cells c. 7–11 μm, medulla not differentiated, cortex not clearly differentiated, cortical cells pale brown c. 3–5 μm.
Perithecia 0.15–0.19 mm diam., 1/2–3/4-immersed, often thinly thalline covered, c. 80–120 perithecia per cm2. Ostiole pale to dark, plane, c. 20–40(–60) μm wide. Involucrellum to the exciple base, c. 30–50 μm thick, appressed to the exciple to slightly diverging at the base, thickening towards the base. Exciple 0.13–0.22 mm, wall pale to rarely dark brown, c. 25 μm thick. Periphyses c. 15–25 × 2–2.5 μm. Asci 8-spored, c. 43–49 × 19–24 μm. Ascospores (12.4–)13.5–14.7–15.9(–17.2) × (5.6–)5.7–6.4–7.1(–7.8) μm (n = 32).
Etymology
Both known localities occur on rocks on the shores of the River Oulankajoki.
Ecology and distribution
The species grows on calcareous and calciferous rocks on shores of the River Oulankajoki in north-eastern Finland. Two localities are known which are c. 12 km apart. One locality is on calciferous schistose rock outcrop and the other is on dolomite stone.
Notes
The species is morphologically most similar to V. norrlinii. Verrucaria norrlinii usually has a thinner involucrellum (usually 15–30 μm thick), but a small number of specimens may have involucrella with a similar thickness to V. oulankajokiensis. Furthermore, dark thalline lines are not found in any studied specimen of V. norrlinii.
Verrucaria oulankajokiensis may also be confused with the species of the V. kalenskyi–V. xyloxena complex, particularly V. kalenskyi and V. raesaenenii (see Pykälä et al. Reference Pykälä, Launis and Myllys2019). These species do not have dark thalline lines and their perithecia are usually not thalline covered. Verrucaria dolosa Hepp has a thinner involucrellum (15–30 μm thick) and ostioles with pale projecting papillae.
Additional specimen examined
Finland: Koillismaa: Kuusamo, Oulanka National Park, Mataraniemi, shore of Oulankajoki River, treeless stony river shore, on dolomite stones, 145 m a.s.l., 66°22ʹN, 29°20ʹE, 2011, J. Pykälä 45173.
Verrucaria vainioi Pykälä & Myllys sp. nov.
MycoBank No.: MB 852439
Differing from V. hunsrueckensis by the thallus of tiny dots.
Type: Finland, Varsinais-Suomi, Lohja, Muijala, Mustalahdentie 100 m W, Lohjanharju esker, Pinus sylvestris-dominated heath forest, VT site type, path, on siliceous pebbles, 102 m a.s.l., 60°17ʹN, 24°12ʹE, 14 November 2020, J. Pykälä 56981 (H9223939—holotype; UPS—isotype). GenBank Accession no.: PP33772.
Thallus medium green, medium brown to dark brown, tiny dots, fleck-like, c. 5–30(–50) μm thick, c. 5–100 μm wide, goniocyst-like units usually present c. 15–35 μm, algal cells c. 5–8 μm, cortex absent to thin, cortical cells hyaline to brown. Prothallus dark brown, fimbriate, often weakly developed.
Perithecia 0.08–0.23 mm, 1/4–1/2-immersed in thallus, c. 40–160 perithecia per cm2. Ostiole tiny, pale to dark, plane to sometimes projecting papillae, c. 15–40 μm wide. Involucrellum to the exciple base, rarely covering only half of the exciple, c. 15–25 μm thick, appressed to slightly diverging near base. Exciple c. 0.12–0.15 mm, wall pale to brown. Periphyses c. 10–25 × 2–3 μm. Asci 8-spored, c. 47–61 × 13–19 μm. Ascospores aseptate, (12.3–)14.8–17.4–20.0(–24.6) × (4.8–)5.5–6.1–6.8(–7.7) μm (n = 89).
Etymology
Named after Edvard August Vainio (1853–1929), a world-famous Finnish lichenologist (Alava Reference Alava, Marcelli and Ahti1998). Vainio also published a monograph of pyrenocarpous lichens in eastern Fennoscandia (Vainio Reference Vainio1921).
Ecology and distribution
Six specimens are known from Southern and Central Finland. The species grows on siliceous pebbles and stones, with one locality on brick on the ground. Verrucaria vainioi may be a pioneer species and often grows on human-influenced sites such as road verges and paths, but it is also found in herb-rich forests without recent human activity. The species may prefer half-shady habitats. Habitats may be rather dry to periodically wet, with the latter potentially affected by some flooding.
Notes
The species is closely related to V. hunsrueckensis as well as to one unidentified specimen (Orange 16504 (NMW), FJ667941). Verrucaria vainioi is also morphologically rather similar to V. hunsrueckensis. However, Verrucaria hunsrueckensis usually has a better developed thallus which is usually rimose or areolate. Nevertheless, a DNA barcode is needed for unambiguous identification of the species. Morphologically, V. vainioi may be most difficult to separate from V. norrlinii but the latter species usually has a larger thallus and, on average, wider spores. Verrucaria danica Servít & M. S. Christ. has slightly smaller perithecia (up to 0.17 mm), an even more reduced thallus and it grows on calcareous rocks.
Additional specimens examined
Finland: Varsinais-Suomi: Lohja, Laakspohja, Eskolantie, abandoned road, road bank, on siliceous pebbles, 60 m a.s.l., 60°15ʹN, 24°08ʹE, 2019, J. Pykälä 52499; Lohja, Paloniemi, Lakimäki S, Picea abies-dominated herb-rich forest, brooklet, on siliceous pebbles, 47 m a.s.l., 60°17ʹN, 23°58ʹE, 2020, J. Pykälä 54604; Lohja, Paloniemi, Palomäki S, Picea abies-dominated herb-rich heath forest, close by a brooklet, on siliceous stone, 62 m a.s.l., 60°17ʹN, 23°58ʹE, 2020, J. Pykälä 54610. Etelä-Häme: Padasjoki, Vesijako Strict Nature Reserve, Hyödynmäki 200 m SE, Picea abies-dominated heath forest, small little-used road, between tracks, on siliceous pebbles, 150 m a.s.l., 61°20ʹN, 25°06ʹE, 2020, J. Pykälä 54650. Pohjois-Savo: Kuopio (Nilsiä), Nilsiä, Iso-Loutteinen E, abandoned gravel pit, field, young mixed forest, on bricks, 150 m a.s.l., 63°13ʹN, 28°02ʹE, 2020, J. Pykälä 55548.
Verrucaria sp.
Notes
These specimens are morphologically similar to V. norrlinii. More genetic markers are needed before their status can be resolved.
Specimens examined
Finland: Pohjois-Karjala: Polvijärvi, Sotkuma, Repovaara, calciferous serpentine rock outcrop, on top, on stone, 100 m a.s.l., 62°47ʹN, 29°20ʹE, 2014, J. Pykälä 47727. Koillismaa: Kuusamo, Kurvinen, Hanhiharju, N of Vasseleenlampi, gravel pit, on serpentine pebbles, 245 m a.s.l., 65°34ʹN, 29°48ʹE, 2006, J. Pykälä 28977; Kuusamo, Liikanen, Oulanka National Park, Korvasvaara, 200 m NW of Kotilaisenlampi, springy brook running through rich fen, on stones, 250 m a.s.l., 66°21ʹN, 29°36ʹE, 2009, J. Pykälä 35945; Kuusamo, Kirkonkylä, Luhtalampi E, small road, ditch bank, on calcareous pebble, 281 m a.s.l., 66°03ʹN, 29°15ʹE, 2020, J. Pykälä 55769. Kittilän Lappi: Kittilä, Sirkka, Kuukerinmaa, abandoned multi-metal ore mine, mine spoil heap, on pebbles, 193 m a.s.l., 67°48ʹN, 24°44ʹE, 2021, J. Pykälä 59214.
Key to the studied species and species with a similar morphology in Finland
1 Thallus often/usually with goniocyst-like units ……… 2
Thallus without goniocyst-like units ……… 11
2(1) Mean spore length 18–23 μm ……… 3
Mean spore length 14–18 μm ……… 4
3(2) Thallus of tiny dots, involucrellum (20–)30–50 μm thick, often thickening to base to 50–70 μm thick ……… ……… V. juankoskiensis Pykälä & Myllys
Thallus occasionally of tiny dots, usually fleck-like, involucrellum (20–)30–40 μm thick ……… V. juumaensis Pykälä & Myllys
4(2) Thallus of tiny dots ……… 5
Thallus fleck-like, rimose to areolate ……… 6
5(4) Perithecia 0.08–0.23 mm; siliceous rocks ……… V. vainioi Pykälä & Myllys
Perithecia 0.11–0.17 mm; calcareous rocks ……… V. danica Servít & M. S. Christ.
6(4) Thallus pale green to dark brown, ostiole often projecting papillae ……… 7
Thallus medium brown to dark brown, ostiole more rarely projecting papillae ……… 9
7(6) Involucrellum 15–30(–40) μm thick ……… V. lapidicola Orange
Involucrellum 30–50 μm thick ……… 8
8(7) Prothallus absent, perithecia rarely leaving pits ……… V. kalenskyi Servít
Fimbriate prothallus often present, perithecia usually leaving pits ……… V. raesaenenii Pykälä & Myllys
9(6) 100–330 perithecia per cm2, aseptate spores occasionally present ……… V. linkolae Pykälä & Myllys
60–230 perithecia per cm2, spores always aseptate ……… 10
10(9) 60–160 perithecia per cm2; calcareous and siliceous rocks ……… V. norrlinii Pykälä & Myllys
80–230 perithecia per cm2; siliceous rocks ……… V. hunsrueckensis Thüs et al.
11(1) Spore length 11–17 μm ……… 12
Spore length mostly 18–25 μm ……… 13
12(11) Involucrellum 30–50 μm thick, ostiole plane ……… V. oulankajokiensis Pykälä & Myllys
Involucrellum 15–30 μm thick, ostiole pale, projecting papillae ……… V. dolosa Hepp
13(11) Thallus areolate, mosaically brown and white ……… V. lohjaensis Pykälä & Myllys
Thallus fleck-like, rimose to more rarely areolate, pale green to dark brown ……… 14
14(13) Perithecia often thinly thalline covered except apex, thallus green to brown ……… 15
Perithecia not thalline covered, thallus brown ……… V. infumata Nyl.
15(14) 50–120 perithecia per cm2, perithecia 1/4–1/2-immersed ……… V. tenebrosa Pykälä et al.
100–200 perithecia per cm2, perithecia 1/4–3/4-immersed ……… 16
16(15) Perithecia 1/2–3/4-immersed, ostiole plane to depressed ……… V. hakulinenii Pykälä & Myllys
Perithecia 1/4–1/2-immersed, ostiole often pale, projecting papillae ……… V. tallbackaensis Pykälä et al.
Acknowledgements
The fieldwork and manuscript preparation were mainly carried out within the research projects ‘Threatened lichens of calcareous rocks’ (grant no YTB059), ‘Key habitats for red-listed lichens’ (grant no 700T-MTX003) and ‘Inventory of calcareous and serpentine rocks’ financed by the Finnish Ministry of the Environment. The first two projects belonged to the research programme of deficiently known and threatened forest species (PUTTE). DNA barcoding was supported by the Kone Foundation, the Finnish Cultural Foundation and the Academy of Finland through their grants to the Finnish Barcode of Life (FinBOL) and the Finnish Biodiversity Information Facility (FinBIF). We would like to thank Emelie Winquist, Diana Weckman and Laura Häkkinen for their help with the laboratory work. The Norwegian specimens were barcoded in the Norwegian DNA lichen barcoding project (OLICH). We are grateful to Einar Timdal for the opportunity to barcode interesting lichen specimens found during the Nordic Lichen Society meeting in 2015 in Steinkjer. Our thanks go out to Mika Bendiksby for her laboratory work with the specimens. We also wish to express our gratitude to the curators of the herbaria B, G, S, UPS and W for the specimen loans and thanks to Andreas Beck, František Bouda, Francesco Di Carlo and Martin Westberg for their hospitality during the visits to M, PRM, VER and UPS, respectively. Herbarium visits were supported by a grant from the Societas pro Fauna et Flora Fennica. The manuscript was improved by the comments of two anonymous referees. We dedicate this paper to Teuvo Ahti in honour of his enormous contribution to lichenology.
Author ORCIDs
Juha Pykälä, 0000-0002-7566-9310; Annina Kantelinen, 0000-0001-8664-7662; Leena Myllys, 0000-0002-9566-9473.
Competing Interests
The authors declare none.
Open access
