identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
03BDA235A4746F7C5A3DA5398DC7FCB8.text	03BDA235A4746F7C5A3DA5398DC7FCB8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fabronia pusilla	<div><p>Fabronia pusilla,  F. rostrata,  F. matsumurae</p><p>The distinction between  F. pusilla and  F. ciliaris is also sometimes questioned. At least some problematic specimens were mentioned by, e.g., Crum &amp; Anderson (1981). Specimens of  F. pusilla from westernmost localities are easily recognized due to large, multicellular teeth at leaf margins. However, at the eastern edge of its distribution range, where  F. pusilla co-occurs with  F. ciliaris, plants with smaller marginal teeth consisting not more than three cells are often collected. Contrary to  F. major and  F. altaica,  F. pusilla usually has ovate leaves abruptly narrowed into acumen, short laminal cells and short, ovate capsules, which is similar to  F. ciliaris . In our dataset, only one specimen of  F. pusilla in question with small marginal teeth was included ( F. pusilla 2, Italy). It appeared in  F. pusilla -clade in ITS-based tree (Fig. 1), belonging the the main haplotype in the haplotype network (Fig. 2). On the other hand, specimens with occasional 2–3-celled marginal teeth were observed far beyond the distributional range of  F. pusilla, e.g., in South Urals and Khabarovsk Territory. They were resolved within  F. ciliaris ( F. ciliaris 20 and 15 in Figs. 1–3).</p><p>We were able to confirm only one specimen of  F. pusilla from Siberia: it is a specimen from Ol’khon Island of Baikal Lake. It is old and could not be sequenced; however, it undoubtfully belongs to this species due to leaves with very large, multicellular marginal teeth (Fig. 10: 4). Closest localities of  F. pusilla are known in Middle Asia (Turkmenistan, Tajikistan and Kyrgyzstan); we confirm these identifications in LE.  Fabronia pusilla was also reported from SW China, Xizang and Yunnan (Gao &amp; Fu, 2002b); however, illustrations in Gao &amp; Fu (2002a: page 96, Fig. 43) do not show the main character of  F. pusilla, namely multicellular teeth at leaf margins.</p><p>Fabronia rostrata is a rare species, only recently found in Russia. The only sequenced specimen showed very subtile difference from  F. ciliaris in ITS and none in more variable IGS1. However, a unique combination of such characters as eperistomate capsule and operculum with long, oblique beak easily separates this species from  F. ciliaris (it is worth to note, however, that one specimen of  F. ciliaris from the Caucasus (Kabardino-Balkaria 1) also had numerous capsules with long, oblique beak, but with perfectly developed peristome). Further studies are needed to understand such discrepancy better.</p><p>Another specimen from the Russian Far East was once identified as  F. matsumurae due to the absence of normally developed peristome. It appeared to be identical to  F. ciliaris in both ITS and IGS1 sequences. Some capsules in this collection have rudimentary or practically absent peristome, while in other ones pale teeth ca. 50 µm long, with papillose-striolate ornamentation were observed. This feature is unknown in  F. ciliaris, but for  F. matsumurae only totally eperistomate capsules were reported. In other characters, i.e., leaf shape, marginal teeth, cell areolation, capsule and operculum shape and spore size these plants fit  F. ciliaris . We consider peristomes in this collection as abnormally developed and refer this specimen to the latter species.</p><p>NrIGS1 vs. nrITS</p><p>The IGS1 is not a very widely used marker for phylogenetic studies as it is often too variable so precluding proper aligning, variable in length (Mateos &amp; Markow, 2005), and has big reversions (Wicke et al., 2011).</p><p>However, in some rapidly evolving groups IGS provides a strong and clear phylogenetic signal, which is well congruent with that from ITS (Logacheva et al., 2011). In moss species of the genus  Schistidium, it possessed a conservative and species-specific substitutions (Milyutina et al., 2015). The present study indicates a great value of IGS1 for supporting ITS-based conclusions of the species delimitation.</p></div>	https://treatment.plazi.org/id/03BDA235A4746F7C5A3DA5398DC7FCB8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Ignatova, Elena A.;Kuznetsova, Oxana I.;Milyutina, Irina A.;Fedosov, Vladimir E.;Ignatov, Michael S.	Ignatova, Elena A., Kuznetsova, Oxana I., Milyutina, Irina A., Fedosov, Vladimir E., Ignatov, Michael S. (2017): The genus Fabronia (Fabroniaceae, Bryophyta) in Russia. Arctoa 26 (1): 11-34, DOI: 10.15298/arctoa.26.02, URL: https://doi.org/10.15298/arctoa.26.02
03BDA235A4766F7C59CBA3E08EF2F880.text	03BDA235A4766F7C59CBA3E08EF2F880.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fabronia Raddi, Atti Accad. Sci. Siena	<div><p>Fabronia Raddi, Atti Accad. Sci. Siena 9: 231–235, pl. 1. 1808.</p><p>Plants very small, soft, forming small flat mats, green or yellowish green, silky. Stems fragile, prostrate, irregularly branched, branches short, mostly densely foliate, julaceous; central strand and hyalodermis not differentiated, all cells ± thin-walled; rhizoids clastered near branch bases and developed on dorsal side of costa in lower part of leaves; paraphyllia absent; juvenile branch leaves narrow lanceolate or linear, sutuated on branch bases. Leaves loosely appressed when dry, occasionally slightly secund, spreading when moist, concave, ovate, ovate-lanceolate or lanceolate, abruptly or gradually acuminate, often piliferous; margins plane, dentate, denticulate or subentire, marginal teeth unicellular, short or long, or large, multicellular; costa slender, ending at midleaf; lamina unistratose, smooth; leaf cells rhomboidal or long-rhomboidal, with moderately thickened, non-porose walls; alar cells differentiated, quadrate and short rectangular, numerous. Autoicous. Perichaetial leaves broader than vegetative leaves. Setae erect, slender, yellowish or brownish, smooth. Capsules erect, ovoid, pyriform or cylindrical; annulus absent; exothecial cells quasrate and short rectangular, with wavy walls, stomata present, with elongate pore; peristome single, consisting of 16 exostome teeth usually fused in pairs, broadly lanceolate, blunt, light brown or dark red-brown, densely papillose-striolate on both surfaces, without trabeculae on both sides, usually reflexed when dry and appressed to the capsule wall, fragile, often broken in opened capsules. Opercula low conic or almost flat, mammillate or obliquely rostrate. Spores small, smooth or finely papillose.</p></div>	https://treatment.plazi.org/id/03BDA235A4766F7C59CBA3E08EF2F880	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Ignatova, Elena A.;Kuznetsova, Oxana I.;Milyutina, Irina A.;Fedosov, Vladimir E.;Ignatov, Michael S.	Ignatova, Elena A., Kuznetsova, Oxana I., Milyutina, Irina A., Fedosov, Vladimir E., Ignatov, Michael S. (2017): The genus Fabronia (Fabroniaceae, Bryophyta) in Russia. Arctoa 26 (1): 11-34, DOI: 10.15298/arctoa.26.02, URL: https://doi.org/10.15298/arctoa.26.02
03BDA235A4766F7D59C3A7E58E12F887.text	03BDA235A4766F7D59C3A7E58E12F887.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fabronia altaica Ignatova & Kuznetsova & Milyutina & Fedosov & Ignatov 2017	<div><p>Fabronia altaica Ignatova &amp; Ignatov,  sp. nova .</p><p>Type: Russia, Altai Republic, Ulagan District, <a href="https://tb.plazi.org/GgServer/search?materialsCitation.longitude=87.98333&amp;materialsCitation.latitude=51.083332" title="Search Plazi for locations around (long 87.98333/lat 51.083332)">left slope to Chulyshman River valley</a> ca. 1 km downstream from Chulcha River mouth, ca. 51°05’N, 87°59’E, 550 m a.s.l., at cliff base in  Rhododendron thickets, on rocks covered with thin layer of soil, 15.VIII.2012, coll. M. Ignatov &amp; E. Ignatova #12-747 (Holotype MHA,  isotypes MW, LE, H, S) .</p><p>Illustrations: Figs. 12, 5: 7–11, 6: 6–10, 8: 7– 12; 11: 14–17.</p><p>Diagnosis: this species is close to  Fabronia ciliaris and differs from it in lanceolate vs. ovate leaves, gradually vs. abruptly acuminate, longer leaf cells: 30–50 µm vs. 20–35 µm long, and ovate-cylindrical vs. ovate capsules.</p><p>Plants small, silky-green, glossy, in dense patches. Stems creeping, ascending at upper part, ca. 5 mm long, irregularly branching; branches 2–3 mm long, erect or arcuate, densely foliate. Stem and branch leaves similar, loosely appressed when dry, straight or ± secund, spreading when moist, ovate-lanceolate or lanceolate, gradually long acuminate, 0.65–0.90 u 0.25–0.30 mm; leaf margins dentate, marginal teeth unicellular, moderate in size (20– 30 µm long); costa slender, smooth, ending at mid-leaf; lamina smooth, upper and median laminal cells elongate-rhomboidal, (29–)35–50(–75) u 7–9 µm, with length/width ratio 4–6:1 and cell length, µm/ leaf length, mm ratio 42.7– 70.9; apical leaf cell to 100 µm long; alar cells quadrate to short-rectangular, forming a weakly delimited rectangular group 3–4 cells wide and 7–11 cells along leaf margin. Autoicous, usually with sporophytes. Perigonia bud-like. Perichaetial leaves ca. 0.8 mm long and 0.4 mm wide, with oblong base and abruptly attenuate narrow acumen; costa ending in the acumen. Sporophytes single in perichaetium. Seta ca. 4 mm long, straight, flexuose when dry, yellow. Capsule ovate-cylindrical, 0.6–0.9 mm long and ca. 0.3 mm wide, slightly constricted below mouth when open, with short neck, smooth, pale brown, with dark-brown rim; annulus absent. Peristome single, consisting of 16 exostome teeth fused in pair, dark-brown, obtuse, ca. 150 µm long; outer surface densely papillose and striolate, inner surface with less prominent ornamentation, smooth in lower part of teeth and covered with low oblique ridges and occasionally with scarce papillae in distal part. Spores 13–15 µm, finely papillose. Operculum low conic, with short oblique beak.</p><p>Distribution and ecology.  Fabronia altaica is known from Altai Republic and the Caucasus, in both regions only from the most xeric areas. In Altai, it grows on dry boulders, rock outcrops and cliffs on xeric slopes, in  Rhododendron thickets at cliff bases and in pine forests; it was also occasionally collected on soil at cliff base. Habitats of this species in Dagestan (Eastern Caucasis) were different: it was collected several times on trunks of birch and pear trees, while in Ingushetia it grew on soil in mixed forest.</p><p>Specimens examined:   RUSSIA: ASIAN RUSSIA: Altai Republic: Ulagan District:  Chulyshman River valley 1 km downstream Chulcha River mouth, 550 m alt., 15.VIII.2012, Ignatov &amp; Ignatova 12-745 (MHA) ;   Shebalino District: Katun River valley near  Ust-Sema, 580 m alt., 28.VII.1991, Ignatov &amp; Ignatova 24/62 (MHA) ;   Chemal District:  Katun River valley 10 km upstream from Chemal, 450 m alt., 7.VII.1993, Ignatov &amp; Ignatova 34/24 (MHA) ;   Edikhta Creek ( Aedigan Creek tributary), 1100 m alt., 8.VII.1993, Ignatov &amp; Ignatova 34/111 (MHA) ;   Ongudai District:  Malyj Yaloman Settl., 900 m alt., 30.VII.1991, Ignatov &amp; Ignatova 25/151 (MHA) ;   Malyj Yaloman Settl., 950 m alt., 30.VII.1991, Ignatov &amp; Ignatova 25/ 158 (MHA) ;   Malyj Yaloman Creek 8.5 km upstream from Katun River, 1100 m alt., 31.VII.1991, Ignatov &amp; Ignatova 25/53 (MHA) ;   CAUCASUS: Dagestan Republic: Gunib District,  Gunib settlement surroundings: 1550 m alt., 22. V.2009, Ignatov &amp; Ignatova 09-725 (MHA, MW) ;  1600 m alt., 21. V.2009, Ignatov &amp; Ukrainskaya 09-475 (MHA);  1560 m alt., 22. V.2009, Ignatov et al. 14095 &amp; 14098 (LE);   Republic of Ingushetia:  Aramkhi, 1300 m alt., 12.VII.2005, Bersanova s.n. (MHA)  .</p><p>? ITALY:Como, 8.IX.1896 &amp; 31.X.1898, F. A.Artaria s.n. (LE). Plants from rich collection with many duplicates (seen in LE, H and S) from the northern Italy (Lombardy) is indistingishable from  F. altaica by morphology. However, some specimens of  F. major from Switzerland (proved by DNA) had laminal cells also more or less similar to  F. altaica (cf. Fig. 7). Considering this, and also the absence of any other specimens of  F. altaica from Central Europe, admitting that this specimen may represent an ultimate modification of  F. major . In the illustrations it is shown under the name  F. cf. altaica .</p><p>Differentiation.  Fabronia altaica is rather variable in leaf shape and size (cf. Fig. 5: 7–11); however, there is rather clear difference in shape from  F. ciliaris: ovate-lanceolate or lanceolate vs. ovate, and more gradually narrowed to the acumen vs. abruptly acuminate. There is a statistically proved difference in cell length between these species (Fig. 7). Fertile plants of  F. altaica are readily distinguished from  F. ciliaris by the shape of capsules: oblong, ovate-cylindrical vs. ovate. Peristome of  F. altaica are usually darker colored, dark-brown vs. light-brown in  F. ciliaris, but this difference may be caused by longer remaining color of peristome in the former species, while in young, deoperculate capsules they are of the same color. Opercula were rarely seen in  F. altaica, but it seems that they are also different, conic and with short oblique beak, while in specimens of  F. ciliaris we observed capsules mainly with mammillate opercula (though some exceptions were also seen: at least one specimen of  F. ciliaris from Kabardino-Balkaria has capsules with obliquely rostrate opercula). In leaf shape,  F. altaica resembles  F. major, and in the beginning of the present study we did not separate them from each other. However, the latter species has longer cells, (36–)50–70(–95) µm (with few exceptions: three specimens from Switzerland had shorter cells, mainly 43–50 µm) but long marginal teeth. See also above the discussion about the specimen from northern Italy which resembles  F. altaica in cell shape but more likely represents a deviating specimens of  F. major . Capsules were found only in few collctions of  F. major; they resemble  F. altaica rather than  F. ciliaris (see Fig. 11: 8–10, 14–17 and 1–7).</p></div>	https://treatment.plazi.org/id/03BDA235A4766F7D59C3A7E58E12F887	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Ignatova, Elena A.;Kuznetsova, Oxana I.;Milyutina, Irina A.;Fedosov, Vladimir E.;Ignatov, Michael S.	Ignatova, Elena A., Kuznetsova, Oxana I., Milyutina, Irina A., Fedosov, Vladimir E., Ignatov, Michael S. (2017): The genus Fabronia (Fabroniaceae, Bryophyta) in Russia. Arctoa 26 (1): 11-34, DOI: 10.15298/arctoa.26.02, URL: https://doi.org/10.15298/arctoa.26.02
03BDA235A4776F67599DA71A89E1FD6B.text	03BDA235A4776F67599DA71A89E1FD6B.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fabronia ciliaris (Brid.) Brid., Bryol. Univ.	<div><p>Fabronia ciliaris (Brid.) Brid., Bryol. Univ. 2: 171. 1827.</p><p>—  Hypnum ciliare Brid., Muscol. Recent. Suppl. 2: 155. 1812.</p><p>Holotype. “Schleicher Botaunte  Fabronia octoblepharis,  Fabronia ciliaris Bryol. Univ. Hypnum [sericeulum?] Helvetia, 1807” (B 31 0677 01), http:// ww2.bgbm.org/Herbarium/specimen.cfm?Barcode= B31067701 (Röpert, 2000).</p><p>Putative isotype in LE: “  Pterigynandrum obctoblepharis Schl., am Nov. genus?, ex Helvet” [another later hardwriting at label bottom “  Fabronia ”].</p><p>Illustrations: Figs. 5: 1–6, 6: 1–5, 11: 1–7; Ignatov &amp; Ignatova (2004): Fig 429 on page 647.</p><p>Plants small, silky-green or yellow-green, glossy, in dense patches. Stems creeping, ca. 5 mm long, irregularly branching; branches 2–3 mm long, erect, densely foliate. Stem and branch leaves similar, loosely appressed when dry, straight, often with slightly recurved apices, spreading when moist, ovate, abruptly long acuminate, 0.5–0.9 u 0.25–0.3 mm; leaf margins denticulate, marginal teeth unicellular, small (ca. 0.1 mm long), or, rarely, consisting of 2–3 cells; costa slender, smooth, ending at midleaf; lamina smooth, upper and median laminal cells rhomboidal, 20–35(–40) u 8–11 µm, with length/width ratio 2–4:1 and cell length, µm/ leaf length, mm ratio 27.0– 53.3; apical cell ca. 110 µm long; alar cells quadrate to short-rectangular, forming weakly delimited rectangular goup 3–4 cells wide and 6–9 cells along leaf margin. Autoicous, sporophytes rare. Perigonia bud-like, sometimes numerous. Perichaetial leaves 0.4–0.5 mm long and 0.3–0.4 mm wide, with oblong base and gradually attenuate narrow acumen; costa ending below apex; margins with longer, stronger recurved teeth in upper part. Sporophytes single in perichaetium. Seta 3–4 mm long, straight, flexuose when dry, yellow. Capsule ovate, with short neck, 0.35–0.45 mm long and 0.3–0.4 mm wide, often flared at mouth with age, smooth, pale brown, concolorous at rim or slightly darker; annulus absent. Peristome single, consisting of 16 exostome teeth fused in pair, light-brown or brown, obtuse, ca. 125 µm long; outer surface papillose-striolate, inner surface with less prominent ornamentation, in distal parts of teeth covered with low vertical ridges. Spores (10–)15–17 µm, papillose. Operculum low conic, mammillate or with short straight or, rarely, moderately long oblique beak.</p><p>Distribution and ecology.  Fabronia ciliaris s. str. is considered as a widespread species throughout the world. It is known from mountain areas of Central and Southern Europe, in Asia it was reported from many provinces of China, from Korea and Japan; it is quite widespread in America, especially in the eastern part, uncommon in Mexico and central South America and becoming more frequent to the south, in mountain areas (Buck, 1983); it was also reported from Australia, New Zealand and Hawai. In Russia,  F. ciliaris is most widespread and frequent species of the genus. It is known from Eastern and Central Caucasus, Middle and South Urals, southern Siberia and south of Russian Far East; its northernmost records were made in southern and central Yakutia and the extreme point is in Verkhoyansk District, at 67°35’N (Isakova, 2010). Most numerous collections were made in Altai Mt. and Transbaikalia. This species grows in mountain areas in a wide range of altitudes, from 150 to 1550 m a.s.l., but mainly in forest zone. It inhabits dry and moderately wet cliffs, rock outcrops and boulders, both acidic and calcareous, in open and shady places, and occasionally grows on soil in rocky places; it was also collected on tree trunks: on poplar in Khabarovk Territory, on elm in Primorsky Territory and on pear trees in Dagestan. In Yakutia, it occurs on rock outcrops on xeric and warm steppe slopes, where other southern xerophilous species where found.</p><p>Selected specimens examined:   RUSSIA: CAUCASUS: Dagestan Republic: Gunib District:  Gunib, 1550 m alt., 22. V.2009, Ignatov &amp; Ignatova 09-672 &amp; 09–766 (MW) ;   North Ossetia /Alania: Suargom Gorge, 800 m alt., 1.XII.2014,  Ukrainskaya 15945 (LE) ;   Kabardino-Balkaria: Chereksky Disrict, Verkhnaya Balkaria Settl., 1100–1150 m alt., 28.VIII.2005,  Ignatov et al. 05-1825 &amp; 05-1880 (MHA) ;   Elbrussky District, Bylym,  Baksan River valley, 1000 m alt., 30.VII.2004,  Ignatov et al. s.n. (MHA) ;   Karachaevo-Cherkessia: Teberda Nature Reserve,  Dzhemagat Creek valley, 1550 m alt., 22.VII.1994,  Onipchenko 115/94 (MW) ;   Aksaut Gorge, 5. VI.1989,  Ukrainskaya 14444 (LE) ;   Daut River valley, 4.VIII.1993, Ukrainskaya 14443 (LE). URALS: Bashkortostan:  Bashkirsky Nature Reserve,  Kaga River mouth, 2.IX.1945,  Selivanova-Gorodkova s.n. (MHA) ;   Chelyabinsk Province: Satka District, Ai River, 300 m alt., 6.VIII.2011,  Ibatullin 36 (MHA) ;   Perm Territory: Kishertsky District,  Kamen Vostryj, 2.VII.1999,  Bezgodov 268 (MW); ASIAN   RUSSIA: Altai Republic: Ulagan District: Chulyshman River valley, 1950 m alt., 2.VIII.1993,  Ignatov 36/95 (MHA) ;   Chulcha River valley, 1000 m alt., 11.VII.1991,  Ignatov 9/12 (MHA) ;   northern shore of Teletzkoe Lake, Yailyu, 460 m alt., 1. VI.1989,  Ignatov 0/1054 (MHA) ;   west of Yailyu, Izvestkovaya Mt., 650 m alt., 12. VI.1989,  Ignatov 0/669 (MHA) ;   Artyshtu River 0.3 km of its mouth, 600 m alt., 20.IX.1989,  Zolotukhin s.n. (MHA) ;   Kukol stow in the valley of Karakem River, 23. VI.1989,  Ignatov 0/1055 (MHA) ;   Sebalino District: Katun River valley near  Ust-Sema, 380 m alt., 28.VII.1991, Ignatov &amp; Ignatova 24/163 (MHA) ;   Chemal District:  Chemal Creek 3 rm upstream mouth, 450 m alt., 12.VII.1993, Ignatov &amp; Ignatova 34/63 (MHA) ;   Irkutsk Province, Irkutsk surroundings, 10.VII.1932,  Kostin s.n. (LE) ;   Baikal Lake, Maloe More,  Yadyrtui Cape, 19.VII.1987,  Bardunov s.n. (LE) ;   Zabaikalsky Territory: Dul’durga District,  Alkhanai National Park,  Ilya River, 8.VII.2006,  Afonina 1606 (LE) ;   Kyra District: Sokhondinsky Biosphere Reserve:  Agutsa River, 1098 m alt., 18.VII.2010,  Afonina A3710 (LE) ;   Enda River, 1320 m alt., 12.VII.2010,  Afonina A1910 (LE) ;   Bukukun River, 1646 m alt.,  Czernyadjeva 42-11 (LE) ;   Ulota District: Ingoda River ner  Leninskiy Settlement, 6.VIII.2011,  Afonina 0611 (LE) ;   Krasnochikoisky District: Zhindokon Creek, 963 m alt., 8.VIII.2011,  Afonina 1411 (LE) ;   Nerchinsk District: Nerchinsko-Kuenginsky Rangem Marikta River, 15.VII.2012,  Czernyadjeva 7-12 (LE) ;   Aleksandrovsky Zavod District, Malaya Borzya River, 817 m alt., 27.VII.2012,  Afonina 4412 (LE) ;   Tungokochin District, Ul’durga River, 618 m alt., 16.VII.2012,  Afonina 1112 (LE) ;   Chita District, Aratsa River, 964 m alt., 13.VII.2012,  Afonina 0312 (LE) ;   Republic of Buryatia: Selenga River near  Novoselenginsk Settlement, 4.VII.2007,  Afonina 00707 (LE) ;   Amurskaya Province: Selemdzhinsky District: Norskaya Hill, 220 m alt., 21. VI.2011,  Bezgodov 391 (MHA) ;   Nora River, 240 m alt., 15.VII.2010,  Bezgodov 460 (MHA) ;   Khabarovsk Territory: Verkhnebureinsky District:  Chegdomyn, 450 m alt.,  Ignatov 97-284 (MHA) ;   Sovgavan District: Botchinsky State Reserve:  Spokoiny Creek, 290 m alt., 22.VIII.2013, Ignatov &amp; Ignatova 13-1035 (MHA) ;   Mulpa River, 245 m alt., 14.VIII.2013, Ignatov &amp; Ignatova 13-494 (MHA) ;   Primorsky Territory: Partizank District:  Chandolaz Mt., 250 m alt., 8.IX.2013,  Ignatov et al. 13-1840 (MHA) ;   Shkotovo District: Ussurijsky Nature Reserve,  Koryavaya Pad’,  Zmeinaya Mt., 331 m alt., 15.X.2008,  Ignatov 08-299 (MHA) ;   Republic of Sakha / Yakutia:  Khangalassky District:  Lenskie Pillars National Park,  Lena River downstream  Labyja Creek mouth, 150 m alt., 19.VIII.2000, Ignatov 00-164 (MHA) ;   Verkhoyansk District, 30 rm W of Tabalakh Settl., Tuostakh Creek, 5.VIII.2009,  Isakova s.n. (MHA)  .</p><p>ASIA: GEORGIA: Borzhom, pr. fl.  Kura, VIII.1877, A.H. &amp; V.F. Brotherus s.n. (LE); Imeretia, pr. fl.  Rion, 6. VI.1877, A.H. &amp; V.F. Brotherus s.n. (LE);   Ossetia, Balta, ad. fl.  Terek, 19. V.1881, A.H. &amp; V.F. Brotherus s.n. (LE).   AZERBAIJAN: Zakatalsky District,  Kebeloba Settl., 14. VI.1969, Lyubarskaya s.n. (LE);   Lenkoran,  Bilyasar Mountains, 28. V.1937, Topachevsky s.n. (LE)  .</p><p>MONGOLIA: Khentii Province, 33 km NW of Dadal,  Bukukun River valley, 4.VIII.2006, Afonina s.n. (LE) ;   Bayan-Hongor Province,  Ikh-Bogd Mt., 2000 m alt., 29. VI.2001,  Ignatov 01-479 (MHA) ;   Omnogovi Province,  Khuren khanyn khep mountain ridge, 2000 m alt., 25. VI.2001,  Ignatov 01-456 (MHA)  .</p><p>CHINA: Inner Mongolia, NE of Huhhot, Yingshan Mountains,  Manhan Mt., 1650 m alt., 24.X.2008, Ignatov 08-511 (MHA)  .</p><p>EUROPE: AUSTRIA: Carinthia: Drautal, Danielsberg, ca. 900 m alt., 14.VI.2003,  Köckinger 15056 (MW, ex Hb. H. Köckinger);   Lavanttal, Waldensteiner Graben E of  Twimberg, 700 m alt., 12.VI.2004, Köckinger 15057 (MW, ex Hb. H. Köckinger);  SWITZERLAND: Ticino, Cugnasco-Gerra, Sciarana, 350 m alt., 9.IV.2005, Schnyder 2005070 (ex Herbarium Norbert Schnyder). HUNGARY: Ktyptogamae exsiccatae #1892, col. Lojka (LE) .   ITALY: Südtirol, Meran, no date,  Zickendrath s.n. (LE)  .</p><p>NORTH AMERICA: U.S.A.: Ohio: Adams Co.,  Spring Glen National Area, 215 m alt., 22. V.2006,  Buck 50414 (NY) ;   Oklahoma: Payne Co., Stillwater Creek, 22.III.1942,  Ikenberry 829 (LE) ;   Missouri: Shannon Co., Jam-Up Creek, 28.XI.1961,  Redfearn 9484 (LE)  .</p><p>Differentiation. Distinctive characters of  F. ciliaris include ovate, abruptly acuminate leaves, regularly denticulate margins with small marginal teeth, short laminal cells 20–45 x 18–11 µm with length/width ratio 2– 4:1 and short, ovate capsules. Its difference from  F. altaica,  F. major,  F. pusilla and  F. rostrata are discussed in comments to them.</p><p>KEY TO IDENTIFICATION OF  FABRONIA SPECIES IN RUSSIA</p><p>1. Leaves ovate, abruptly long acuminate; leaf length/ width ratio 2.4–2.8:1 ............................................. 2</p><p>— Leaves ovate-lanceolate or lanceolate, gradually long acuminate; leaf length/width ratio (2.4–)2.8–3.7:1 .. 4</p><p>2. Marginal teeth unequal, large 3–5-celled teeth alter with small unicellular teeth ......................  F. pusilla</p><p>— Marginal teeth equal, small, 1(–2)-celled ............. 3</p><p>3. Peristome present .....................................  F. ciliaris</p><p>— Peristome absent ............................ [ F. matsumurae]</p><p>4(1) Peristome absent; operculum with a curved long beak; leaf margins finely serrulate .........  F. rostrata</p><p>— Peristome present; operculum with a short beak or mammillate; leaf margins serrate .......................... 5</p><p>5. Upper and middle leaf cells 50–70(–85) µm long, 4– 8:1; teeth at leaf margins 25–50 µm long ....  F. major</p><p>— Upper and middle leaf cells 35–50 µm long, 4–6:1; teeth at leaf margins 20–30 µm long ..........  F. altaica</p></div>	https://treatment.plazi.org/id/03BDA235A4776F67599DA71A89E1FD6B	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Ignatova, Elena A.;Kuznetsova, Oxana I.;Milyutina, Irina A.;Fedosov, Vladimir E.;Ignatov, Michael S.	Ignatova, Elena A., Kuznetsova, Oxana I., Milyutina, Irina A., Fedosov, Vladimir E., Ignatov, Michael S. (2017): The genus Fabronia (Fabroniaceae, Bryophyta) in Russia. Arctoa 26 (1): 11-34, DOI: 10.15298/arctoa.26.02, URL: https://doi.org/10.15298/arctoa.26.02
03BDA235A4686F665A3DA64A8E1FFC72.text	03BDA235A4686F665A3DA64A8E1FFC72.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fabronia major DeNot., Mem. RealeAccad. Sci. Torino	<div><p>Fabronia major DeNot., Mem.RealeAccad.Sci.Torino 39: 229. 1836.</p><p>— Fabronia pusilla var. major (De Not.) Schimp., Bryol. Eur. 5: 71 (fasc. 44–45. Mon. 3). 1850.</p><p>Lectotype (selected here): specimen from herbarium of G. Hampe, BM 001007509 (Fig. 14).</p><p>Comments on the lectotypification: there are two specimens of  Fabronia major in BM, which obviously belong to the same species (Fig. 14). Collection from the Hampe herbarium is preferred by the following reasons, suggested by Len Ellis: (1) it has several sporophytes (in Schimper’ herbarium only one or two); (2) specimen from Hampe’ herbarium is generally in a better physical condition; (3) specimen from Schimper’ herbarium includes fragments of a different pleurocarp with leaves with conspicous single costa (superficially similar to  Lescurea saxicola), while the specimen from Hampe herbarium has no admixtures.</p><p>Illustrations: Figs. 13–14, 5: 12–16, 6: 11–14, 8: 13– 15 and 11: 8.</p><p>Plants small, yellow-green, green or grayish-green, glossy, in soft, dense patches. Stems creeping or ascending, 5–10 mm long, irregularly branching; branches 2–4 mm long, straight or arcuate, densely foliate. Stem and branch leaves similar, loosely appressed when dry, straight, occasionally secund, erect-spreading when moist, lanceolate, gradually long acuminate, 0.6–1.0(– 1.3) u 0.2–0.3(–0.4) mm; leaf margins dentate or ciliate, marginal teeth mainly unicellular (occasionally with additional short cell at base, long (25–35 µm, occasionally to 50 µm long); costa slender, smooth, ending at midleaf; lamina smooth, upper and median laminal cells elongate-rhomboidal, (36–)50–70(–85) u 8–11 µm, with length/width ratio 4–8:1 and cell length, µm/ leaf length, mm ratio 42.8–91.2; apical leaf cell to 175 µm long; alar cells quadrate to short-rectangular, forming weakly delimited rectangular goup 3–4 cells wide and 8–13 cells along leaf margin. Autoicous, sporophytes infrequent. Perigonia bud-like. Perichaetial leaves 0.5–0.7 mm long and ca. 0.2 mm wide, with oblong base and gradually attenuate narrow acumen; costa ending above midleaf; margins with stronger dentate in upper part than stem leaves. Sporophytes single in perichaetium. Seta 3–4 mm long, straight, flexuose when dry, yellow. Capsule short cylindrical, with short neck, 0.7–0.8 mm long and 0.4– 0.5 mm wide, occasionally flared at mouth with age, smooth, light brown, with dark-brown rim; annulus absent. Peristome single, consisting of 16 exostome teeth fused in pair, dark-brown, obtuse, ca. 125 µm long, with few round perforations in distal part; outer surface papillose-striolate, inner surface with less prominent ornamentation, with low vertical ridges. Spores 14–17 µm, brownish, papillose. Operculum low conic or almost flat, with very short, narrow, straight beak.</p><p>Distribution and ecology.  Fabronia major was found in collections from the Eastern Caucasus (Dagestan and North Ossetia) and Central and Southern Europe (Austria, Switzerland and northern Italy). It grows in mountain areas at low and middle altitudes, up to 1100 m a.s.l. in the Alps and up to 1600 m in the Eastern Caucasus. In Dagestan it was collected on trunks of hornbeam and pear trees; one specimen was also gathered from the trunk of  Magnolia and another on unknown tree in the cemetery in Switzerland. All other collections were made from siliceous cliffs and boulders, shady and open. Most Caucasian collections were sterile, while in the mountains of Central Europe sporophytes were occasionally present.</p><p>Specimens examined:   RUSSIA: Dagestan Republic: Gunib District,  Gunib Settlement surroundings: 1370 m alt., 19. V.2009, Ignatov &amp; Ignatova 09-254 (MHA);  1600 m alt., 21. V.2009, Ignatov &amp; Ukrainskaya 09-472 (MHA);  Republic of Severnaya Ossetia /Alania:  North Ossetian Nature Reserve, Tsei River valley, 25.VII.1979, L. I. Abramova s.n. (MW);  Fiagdon Gorge, 1275 m alt., 13.VII.2015, Ukrainskaya 16660 (LE);  Nizhny Lars, 800 m alt., 1.VII.2014,  Ukrainskaya 15938 (LE)  .</p><p>AUSTRIA: Styria:  Stadl an der Mur, 1100 m alt., 11.X.1993, Köckinger s.n. (MW, ex Hb. H. Köckinger) ;   bei  St. Michael, 600 m alt., 7.VII.1884, Breidler s.n. (LE) ;   Upper Austria: Donautal,  Schlögen, 350 m alt., 2.X.2013, Köckinger 14991 (MW, ex Herb. H. Köckinger) ;   Carinthia,  Lavant valley, between Twimberg and Waldenstein, 650 m alt., 18.IV.2001, Köckinger 14992 (MW, ex Hb. H. Köckinger)  .  SWITZERLAND: Zürich, 418 m alt., 29.III.2015, Kiebacher 781 (MW, ex Herb. T. Kiebacher);   Ticino: Muralto, am  Lago Maggiore, 196 m alt., 11.X.2002, Hofmann s.n. (MW, ex Herb. H. Hofmann) ;   Vogomo, 510 m alt, 7.VII.2001,  Hofmann s.n. (MW, ex Herb. H. Hofmann) ;   Monte Carasso,  Pedemonte, 395 m alt., 9.IV.2005, Schnyder 2005052 (MW, ex Herb. Norbert Schnyder) ;   Grisons,  Bregaglia, 890 m alt., 12.X.2016, Hofmann s.n. (MW, ex Herb. H. Hofmann)  .   ITALY: Piedmont, Lepontine-Verbano Alps,  Cicogna, 740–750 m alt., 24.VII.2012, Kučera 15135 (CBFS)  .</p><p>Differentiation.  Fabronia major was taken for both  F. pusilla and  F. ciliaris, since it considered as a variety of the former and a synonym of the latter. It resembles  F. pusilla in long marginal teeth which, however, are unicellular, like in  F. ciliaris . At the same time, it can be readily distinguished from both these species by narrow, lanceolate vs. ovate leaves and much longer, elongate-rhomboidal laminal cells with length/width ratio 4–8:1 vs. 2–4:1. It resembles  F. altaica in leaf and capsule shape, but that species has slightly shorter cells, 4–6:1, and shorter marginal teeth. There is some similarity in leaf shape, cell length and strong serration of leaf margins between  F. major and South and Central American  F. macroblepharis Schwägr., but the latter species has even longer marginal teeth which are often 2–3-celled.</p></div>	https://treatment.plazi.org/id/03BDA235A4686F665A3DA64A8E1FFC72	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Ignatova, Elena A.;Kuznetsova, Oxana I.;Milyutina, Irina A.;Fedosov, Vladimir E.;Ignatov, Michael S.	Ignatova, Elena A., Kuznetsova, Oxana I., Milyutina, Irina A., Fedosov, Vladimir E., Ignatov, Michael S. (2017): The genus Fabronia (Fabroniaceae, Bryophyta) in Russia. Arctoa 26 (1): 11-34, DOI: 10.15298/arctoa.26.02, URL: https://doi.org/10.15298/arctoa.26.02
03BDA235A46C6F6659C3A3D68F80F839.text	03BDA235A46C6F6659C3A3D68F80F839.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fabronia pusilla Raddi, Atti Accad. Sci. Siena	<div><p>Fabronia pusilla Raddi, Atti Accad. Sci. Siena 9: 231. 1808.</p><p>Type. Europe: Toscana, Raddi s.n.</p><p>Illustrations: Figs. 9: 1–6, 10: 1–5 &amp; 11: 11–13; see also Ignatov &amp; Ignatova (2004), Fig. 430 on page 648.</p><p>Plants very small, soft, yellowish green, glossy, in small dense tufts. Stems creeping, ascending at apex, irregularly branched; branches erect, 1–2 mm long, densely foliate. Leaves loosely appressed when dry, often with recurved piliferous acumen, occasionally slightly secund, spreading when moist, ovate, abruptly long acuminate, 0.50–0.80 u 0.15–0.35 mm; leaf margins coarsely dentate to ciliate, marginal teeth unequal, large 3–5-celled teeth alter with small unicellular teeth; costa slender, smooth, ending at mid-leaf; lamina smooth, upper and median laminal cells rhomboidal, 25– 30(–45) u 9–11 µm, with length/width ratio 3–4:1 and cell length, µm/ leaf length, mm ratio 31.8–49.6; apical leaf cell to 110 µm long; alar cells quadrate to short-rectangular, forming weakly delimited rectangular goup 3–4 cells wide and 6–11 cells along leaf margin. Autoicous, sporophytes infrequent. Perigonia bud-like. Perichaetial leaves ca. 0.5 mm long and 0.2 mm wide, with oblong base and gradually attenuate narrow acumen; costa ending at midleaf; margins moderately dentate in upper part. Sporophytes single in perichaetium. Seta 2–3 mm long, straight, yellow. Capsule ovate, with short neck, 0.4–0.6 mm long and 0.3– 0.4 mm wide, smooth, light brown, concolorous at rim; annulus absent. Peristome single, consisting of 16 exostome teeth fused in pair, light brown, obtuse, ca. 75 µm long; outer surface papillose-striolate, inner surface with less prominent ornamentation, with low vertical ridges. Spores 12– 14 µm, brownish, papillose.Operculum low conic, with short oblique beak or mammillate.</p><p>Distribution and ecology. Main distribution area of  Fabronia pusilla is in the western parts of Eurasia and North America, with southernmost localities in Mexico, and in northern Africa. It was also reported from southwestern provinces of China and states of Middle Asia. In Russia it is known from two localities: in Rostov Province (south of European Russia) and in Republic of Buryatia (Asian Russia, Baikal Lake area). Both places are characterized by xeric conditions. In Rostov province  F. pusilla was collected on dead wood in the park. In Buryatia it grew on the shore of Baikal Lake (Svyatoi Nos peninsula), in deep shady niches of dry cliffs, on eroded rock surface. In the main part of its area,  F. pusilla grows mainly on dry rocks (volcanic, granite, limestone), but is occasionally collected from tree trunks (e.g., of  Quercus pubescens).</p><p>Specimens examined: RUSSIA: EUROPEAN RUSSIA: Rostov Province: Rostov-na-Donu, Kamenka Settlement, park of the health resort “Rostovsky”, 16.X.2000,  Sereda s.n. (MHA); ASIAN RUSSIA: Republic of Buryatia: NE shore of Baikal Lake, Svyatoi Nos peninsula, 450 m alt, 26. VI.1956, Bardunov s.n. (LE).</p><p>EUROPE: SPAIN: Granada, Sierra Nevada, Güejar Sierra, Vereda de la Estrella, 145 m alt., 21. V.2009,  Guerra 30176 (LE); Andalucia, Grazalema, Sierra del Endrinal, 350 m alt., 3. V.2015, Kučera 17500 (CBFS). ITALY: South Tyrol: Etschtal, Castel Feder S of Auer, 350 m alt., 29.X.1989 Köckinger s.n. (MW, ex Herb H. Köckinger); prope Bozen, 260 m alt., Sauter, Flora Exsiccata Austro-Hungarica #717 (LE). SWITZERLAND: Ticino, Lugano, 280 m alt., 11.II.2003, Schnyder 2003001 (MW, ex Herb. Norbert Schnyder). AUSTRIA: Styria orientalis, Hartberg, 450 m alt., X.1942, Baumgartner, Crypt. Exs. ed. a Museo Hist Natur. Vindobonensi #892 (LE).</p><p>ASIA: TADJIKISTAN: Darvaz Ridge, Pyandzh River basin, Egit Village, Surkh-Dara gorge, 1130 m alt., 9.VII.1964, Mamatkulov 5218 (LE). KYRGYZSTAN: Kyrgyz Range, Dzhirly-Kaindy stow, 1900 m alt., 18. VI.1965, Rakhmatullina s.n. (LE).</p><p>NORTH AMERICA: U.S.A.: Colorado, Boulder Co., Nordseite des Boulder Canyon, 2150 m alt., 30.III.1957,  Weber, Crypt. Exs. ed. a Museo Hist Natur. Vindobonensi #4476 (LE); California: Mariposa Co., Elephant Rock, ca. 975 m alt., 2.XII.2006, Shevock 29285 (NY); San Benito Co., ca. 470 m alt., 12.II.2005, Shevock 26293 (NY); Monterey Co., San Antonio Reservoir County Recreation Area, ca. 240 m alt., 3. I.2009, Schevock 32581 (NY); Oregon: Wheeler Co., John Day River basin, 655 m alt., 23.III.2008, Shevock 31600 (NY); Wasco Co., Colombia River Gorge National Scenic Area, 45 m alt., 27.III.2008, Shevock 31659 (NY).</p><p>Differentiation. ‘Typical’ specimens of  Fabronia pusilla are easily recognized due to large, multicellular teeth at leaf margins. However, some specimens with smaller, 2–3-celled teeth may be referred either to  F. pusilla or  F. ciliaris (as it is proved by DNA data) and cannot be identified with confidence. Such specimens were observed mainly in Central Europe where both species co-occur. Maybe slightly smaller spores of  F. pusilla, 12–14 vs. 15–17 µm in  F. ciliaris, can help in these difficult cases.</p></div>	https://treatment.plazi.org/id/03BDA235A46C6F6659C3A3D68F80F839	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Ignatova, Elena A.;Kuznetsova, Oxana I.;Milyutina, Irina A.;Fedosov, Vladimir E.;Ignatov, Michael S.	Ignatova, Elena A., Kuznetsova, Oxana I., Milyutina, Irina A., Fedosov, Vladimir E., Ignatov, Michael S. (2017): The genus Fabronia (Fabroniaceae, Bryophyta) in Russia. Arctoa 26 (1): 11-34, DOI: 10.15298/arctoa.26.02, URL: https://doi.org/10.15298/arctoa.26.02
03BDA235A46D6F67599DA0B08E45F8C6.text	03BDA235A46D6F67599DA0B08E45F8C6.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Fabronia rostrata Broth., Symb. Sin.	<div><p>Fabronia rostrata Broth., Symb. Sin. 4: 92. 1929.</p><p>Type. China: Yunnan, Mekong, 28°11’N, Handel-Mazzetti 8018 (holotype H) .</p><p>Illustrations: Figs. 9: 11; 10: 9 and 11: 20; see also Dudov et al., 2015.</p><p>Plants small, in flat, loose or moderately compact mats, light green or grayish, glossy. Stems 10–15 cm, prostrate, irregularly branched, evenly foliate. Leaves appressed and imbricate when dry, erectopatent to spreading when wet, 0.6–1.0(–1.2) u 0.4–0.5 mm, ovate-lanceolate, gradually narrowed into a long and narrow acumen, slightly concave; margins plane, finely serrulate; costa slender, reaching 0.4–0.6 of leaf length; laminal cells rhomboidal, thin-walled, smooth, 30–60 u 6–10 µm, with length/width ratio 2–4:1 and cell length, µm/ leaf length, mm ratio 19.5–33.7; apical leaf cell to 110 µm long; alar cells differentiated, quadrate, in 3–4 rows at margin. Autoicous. Seta 2–3 mm. Capsule ovoid, 0.6– 0.9 mm long. Operculum almost flat, with rather long oblique beak. Peristome totally reduced. Spores 10–15 µm.</p><p>Distribution and ecology.  Fabronia rostrata was originally collected in NW Yunnan, at 2325 m a.s.l., on granite rocks in a dry oxbow of Mekong River (Brotherus, 1929). Gao &amp; Fu (2002) report the species from another locality in Yunnan and from Henan, describing its habitats as “rocks and tree trunks in forests”. In Zabaikalsky Territory the species grew at low elevation, up to 650 m a.s.l., on rock outcrops; in Amurskaya Province it was collected at 400–650 m a.s.l., on rock in the forest and on  Tilia amurensis trunk.</p><p>Specimens examined: RUSSIA: Zabaikalsky Territory, Nerchinsko-Zavodskiy District, near Nerchinsky Zavod settlement, 658 m alt., 25.VII.2012, Afonina 3912 (LE); Amurskaya Province: Zeisky Disctrict, Zeya Nature Reserve, Tukhuringra range: Gilyiskiy bay of Zeya reservoir, right shore, at 0.3 km to W from cordon “Medvezhiy” 628 m alt., 2.VIII.2013, Dudov &amp; Kotel’nikova# 2013_Br_0021; Izvestkoviy bay of Zeya reservoir, right shore near Izvestkoviy stream estruary 421 m alt., 4.VIII.2013. Dudov &amp; Kotel’nikova 2013_Br_0336 (MW).</p><p>Differentiation. In the description of this species V.F. Brotherus (1929) noted such characteristic features of the species as finely serrulate leaf margins and operculum with rather long oblique beak. These characters, as well as the absence of peristome, allow its separation from both  F. ciliata and  F. pusilla which possess much stronger serrate leaf margins (especially the latter species), mammillate operculum and well-developed, albeit fragile single peristome of 16 teeth, strongly reflexed in dry state and appressed to the urn of opened capsules. Even if partly brocken, teeth remains are apparent enough to indicate peristome presence in these species.</p></div>	https://treatment.plazi.org/id/03BDA235A46D6F67599DA0B08E45F8C6	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Ignatova, Elena A.;Kuznetsova, Oxana I.;Milyutina, Irina A.;Fedosov, Vladimir E.;Ignatov, Michael S.	Ignatova, Elena A., Kuznetsova, Oxana I., Milyutina, Irina A., Fedosov, Vladimir E., Ignatov, Michael S. (2017): The genus Fabronia (Fabroniaceae, Bryophyta) in Russia. Arctoa 26 (1): 11-34, DOI: 10.15298/arctoa.26.02, URL: https://doi.org/10.15298/arctoa.26.02
