54 BRYOLOGICAL NOTES Piippo S. 1985. Bryophyte flora of the Huon Peninsula, Papua New Guinea. XII. Geocalycaceae (Hepaticae). Acta Botanica Fennica 131: 129–167. Piippo S. 1990. Annotated catalogue of Chinese Hepaticae and Anthocerotae. Journal of the Hattori Botanical Laboratory 68: 1–190. Tan BC, Engel JJ. 1986. An annotated checklist of Philippine Hepaticae. Journal of the Hattori Botanical Laboratory 60: 288– 355. Yamada K, Iwatsuki Z. 2006. Catalog of the Hepatics of Japan. Journal of the Hattori Botanical Laboratory 99: 1–106. D. K. SINGH, Botanical Survey of India, CGO Complex, 3rd MSO Building, Block F (5th floor), Salt Lake Sector I, Kolkata 700 064, India. E-mail: singh_drdk@rediffmail.com DEVENDRA SINGH, Botanical Survey of India, Central National Herbarium, Howrah 711 103, India Journal of Bryology (2009) 31: 54–62 # British Bryological Society 2009 Received 16 November 2008. Revision accepted 23 November 2008 DOI: 10.1179/037366808X343711 New national and regional bryophyte records, 20 Intending contributors to this column should consult the Instructions for Authors in part 1 of this volume, and should address their contributions to the column editor. 1. Andrewsianthus marionensis (S.W.Arnell) Grolle Contributors: Jiřı́ Váňa, Ryszard Ochyra, Marc Lebouvier and Beata Cykowska Îles Kerguelen: GRANDE TERRE: Péninsule Courbet, southern side of Val Studer: plateau at the upper part of the gorge with the cascade above the hut at the south-eastern end of Lac Supérieur, 49u17944.899S, 70u03900.799, 357 m a.s.l., in open places in fell-field on gravelly soil in dry situation, amongst Dicranoloma kerguelense and Jamesoniella colorata, 28 December 2006, leg. R. Ochyra No. 3727d/06 (KRAM). Hitherto, Andrewsianthus marionensis has been known only from three widely separated regions in the Southern Ocean. It was originally described from subantarctic Marion Island as Cephaloziella marionensis (Arnell, 1952) and a year later this author described another specimen from the same island as Lophozia marionensis (Arnell, 1953). Surprisingly, he had described a separate species using the same specific epithet. The two taxa were considered conspecific by Grolle (2002) who in the meanwhile transferred C. marionensis to the genus Andrewsianthus (Grolle, 1971). Váňa (1985) extended the range of A. marionensis to Tristan da Cunha when reducing Lophozia squarrosa S.W.Arnell to synonymy with the former species name. Additionally, A. marionensis is known from Île de la Possession in the Îles Crozet archipelago (Grolle, 2002) and now its range is extended to the largest archipelago in the Subantarctic, Îles Kerguelen. Thus, at present A. marionensis may be considered as a subantarctic species, nearly-endemic to the Kerguelen Province, only slightly extending to the southern cool-temperate zone in the Southern Atlantic Ocean sector. With the discovery of this species the known liverwort flora of Îles Kerguelen is increased to 38 species (Váňa & Gremmen, 2006). 2. Brachythecium rivulare Schimp. Contributor: C.C. Townsend Tanzania: ARUSHA DISTRICT: Nasolo River, E. slope of Mount Meru 3u149S, 36u459E, forming a dense mat on volcanic rocks on a broken cliff at the foot of a waterfall above a pool full of Zannichellia palustris and in the full spray of the fall, saturated with slightly alkaline water, 1820 m a.s.l, 14 March 1968, Greenway & Kanuri 13391 (EA, Priv. Herb. Townsend). This specimen displays the usual form of mosses growing in the full spray of a waterfall in having a dense mat of stems with leaves for the most part reduced to the costa. However, on soaking out it is possible to find leaves here and there which show the normal leaf shape of this species, with a rather short apex and the typical enlarged cells at the basal angles often forming distinct auricles. The locality is the same as that from which Drepanocladus aduncus (Hedw.) Warnst. was recorded (Townsend, 2007). The only previous record of the species from tropical Africa appears to be from Mount Kenya. 3. Bryum pallens Sw. Contributor: C.C. Townsend Zambia: NORTH-WESTERN PROVINCE: Mwinilunga District, on rocks in the R. Zambesi, Zambesi Rapids, 6 km N. of Kalene Hill, 11u109S, 24u119E, ca 1350 m a.s.l., 20 February 1975, leg. Townsend 75/174 (Priv. Herb. Townsend). At this point the Zambesi is only a few metres wide, and readily wadeable although fast-flowing; it much resembles the kind of stream that could be found almost anywhere in Europe containing B. pallens. Only the stem of this gathering shows any red colouration, and it very much resembles in this and all other respects another collection made in flushes on Ben Sgulaird, Glen Creran, Argyll, Scotland, 833 m a.s.l., Townsend 72/318 (Priv. Herb. Townsend). 4. Bucklandiella lamprocarpa (Müll.Hal.) Bednarek-Ochyra & Ochyra Contributors: Halina Bednarek-Ochyra and Ryszard Ochyra BRYOLOGICAL NOTES Bolivia: DEPARTAMENTO LA PAZ: Inquisivi Province, small lake called locally Laguna Huichincani, ca 1 km south of Rı́o Glorieta along trail from Bicupaya and Mina Huichincani, ca 8.5 km north-west of Quime, 16u579S, 67u179W, 400024020 m a.s.l, seeps over cliff by waterfall, 19 May 1987, leg. M. Lewis 87479 (KRAM, MO). The rheophytic Bucklandiella lamprocarpa has so far exhibited bicentric distribution in South America. It is widely distributed and locally common and abundant in the temperate regions in the southern part of the continent, extending to lat. ca 34uS in central Chile (Bednarek-Ochyra & Ochyra, 1994; Bednarek-Ochyra, Matteri & Ochyra, 1996) and then, after a significant gap in its range, recurring in northern South America at altimontane elevations in the Andes of Venezuela and Colombia (Churchill, Griffin & Muñoz, 2000), Ecuador (Bednarek-Ochyra, Ochyra & Soldán 2002) and northern Peru (Menzel, 1986). It is worth noting that the Peruvian plants were re-determined as B. bartramii (Roiv.) Roiv. by Deguchi (1987) but this is an incorrect conclusion since the latter is a distinct species endemic to the Fuegian region which differs at once from B. lamprocarpa in its spherical capsules (Ochyra, Sérgio & Schumacher, 1988). The discovery of B. lamprocarpa in Bolivia was expected since many cool-adapted austral species that penetrate into the northern Andes have intermediate stations in the Central Andes. 5. Campylopus introflexus (Hedw.) Brid. Contributor: Özlem Tonguç Yayintaş Turkey: THRACE REGION: Istranca Mountains, between Dereköy and Demirköy villages, 41u429–42u019N, 27u309– 28u049E, 350 m a.s.l., under mixed forest, base of trees, associated with Dicranum montanum Hedw., 5 February 2004, leg. Özlem Tonguç Yayintaş T 1472, conf. T.L. Blockeel (MO, Çanakkale Onsekiz Mart University herbarium). Campylopus introflexus is not included in the recent checklists of the moss flora of Turkey (Çetin & Uyar, 2004; Kürschner & Erdağ, 2005), and the present report is the first for the country. It is a widespread species in western Europe, occurring commonly in Britain and Ireland and extending to northern Iceland (Jóhannsson, 1991), Spain (Casas, 1991), Italy (Cortini Pedrotti, 2001), southern Scandinavia, and eastwards to Austria (Grims, 1999), the Czech Republic (Kučera & Váňa, 2003; Mikulášková, 2006), Slovakia (Holotová & Šoltés, 1997), Poland (Stebel, 1995; Fojcik & Gumieniak, 1999), Kaliningrad Province in Russia (Razgulayeva et al., 2001) and Hungary (Szűcs & Erzberger, 2007). The Istranca Mountains in Thrace are influenced by a sub-Mediterranean climate, and support Euro-Siberian, Euxine and Hyrcano-Euxine floristic elements (Yarcı, 2000). Common trees in the sampling area include Corylus avellana L. var. avellana, Fagus orientalis L., Acer sp., Cornus mas L., Quercus frainetto Ten., and Q. cerris L. 55 6. Coscinodon cribrosus (Hedw.) Spruce Contributor: Peter Erzberger Hungary: MEDVES MTS: County of Nógrád, on the south face of the basalt rock ‘Nagy-Kő’ near Bárna, east of Salgótarján, 48u05935.799N, 19u57907.599E, ca 500 m a.s.l., in crevices of the vertical basalt rock, leg. P. Erzberger 12830, 24 March 2008, conf. E. Maier April 2008 (B). Coscinodon cribrosus was excluded from the recent checklist of the bryophytes of Hungary (Erzberger & Papp, 2004) because earlier reports were based on misidentifications. Therefore, the above-mentioned collection is the first confirmed record for Hungary. 7. Didymodon rigidulus Hedw. Contributor: C.C. Townsend Kenya: NORTH NYERI DISTRICT: Ol’Loigululu Farm, Nanyuki, corticolous on tree by the Rongai river, ca 1880 m a.s.l., 22 January 1985, leg. C.C. Townsend 85/241. Tanzania: MBEYA DISTRICT: on bank by track, Isyonje village, 8u599S, 33u37.59E, Poroto Mts., ca 2200 m a.s.l., 29 May 1980, leg. C.C. Townsend 80/192; UFIPA DISTRICT: on a wall in the boma, Sumbawanga, 7u57.59S, 31u379E, ca 1450 m a.s.l., 4 June 1980, leg. C.C. Townsend 80/276. All specimens of this species are det. P. Sollman and are in Priv. Herb. Sollman & Priv. Herb. Townsend. 8. Didymodon sicculus M.J.Cano, Ros, Garcia-Zamora & J.Guerra Contributors: Marko Sabovljević and Aneta Sabovljević Slovenia: Coastal region, by local road between Piran (Pirano) and Portoroz (Portorose), 45u34.5659N, 13u32.8319E, leg. Marko Sabovljević & Aneta Sabovljević, 22 April 2008 (BEOU no. 4724). Didymodon sicculus was described by Cano et al. (1996) as an endemic species to the Iberian peninsula. However it was subsequently discovered in other circumMediterranean territories, though its extended range remains scattered: Spain (Cano et al., 2001), southern and northern Greece (Blockeel et al., 2002; Sabovljević, Tsakiri & Sabovljević, 2008), continental Italy and Sicily (Aleffi, Sabovljević & Tacchi, 2003; Puglisi, Privitera & Prezzavento, 2004), Turkey (Papp & Sabovljević, 2003; Jimenez et al., 2004), Montenegro (Cvetić & Sabovljević, 2004), Algeria, The Azores, The Canary Islands, Israel and Yemen (Jimenez et al., 2004). It was recorded for the first time in Slovenia along a minor road at the edge of pine forest on sunny or partially shaded loamy dry soils. Other species recorded in similar situations at the same site were Didymodon acutus (Brid.) K.Saito and Dicranella howei Renauld & Cardot. It is unlikely that D. sicculus is limited to this one site in Slovenia, but the new site and those in Greek Chalkidiki represent the northern limits of its range, here always close to the coastline. With further investigation it will probably be discovered in Croatia and Albania, and also in some dry inner territories where Mediterranean influence is high. 56 BRYOLOGICAL NOTES 9. Fissidens arnoldii R.Ruthe Contributors: A. Erdağ and H. Kürschner Turkey: PROVINCE ERZINCAN: KEMALIYE, Munzur Daglari, south-west of Erzincan, Kemaliye, between Salihli Köyü and Kemaliye, Esartepe, 39u17939.799N, 38u29926.499E, 870 m a.s.l., on soil-covered serpentine rock and in rock crevices in Quercus woodland, 14 May 2006, leg. A. Erdağ 06/ 233b (AYDN and Priv. Herb. H. Kürschner). A temperate taxon distributed in Europe (from Belgium, France, and the Netherlands through the lower parts of Central Europe to Poland and Russia (Frey et al., 2006)) and South-West Asia (Iraq, Israel, Jordan, Kuwait, Oman, Saudi Arabia, United Arab Emirates, Yemen (Kürschner, 2008)). At present no records are known from the West and South Mediterranean. The nearest site to the new Turkish locality is situated in northern Iraq [Mosul liwa: Turkish border near Sharanish, in Quercus woodland above Basingera (Fröhlich, 1959)]. The Turkish plants collected in Kemaliye clearly show the typical characters of F. arnoldii, i.e. (1) leaves in 3–8 pairs, ovate-oblong, obtuse and apiculate, (2) limbidia absent, (3) upper part of leaf much shorter than vaginant part. The species grows on soil-covered serpentine rocks, in rock fissures, hollows and clefts in shady but somewhat xeric conditions in Quercus infectoria subsp. boissieri woodland. Accompanying species are Encalypta rhaptocarpa Schwägr., Entosthodon fascicularis (Hedw.) Müll.Hal., E. muhlenbergii (Turner) Fife, Homalothecium sericeum (Hedw.) Schimp., Pseudocrossidium hornschuchianum (Schultz) R.H.Zander, Reboulia hemisphaerica (L.) Raddi and Weissia controversa Hedw., all affected by excess run-off from the smooth rock faces after rainfall. 10. Fossombronia echinata Macvicar Contributors: M. Kirmaci and A. Erdağ Turkey: PROV. AYDIN: Germencik county, Çamlık village, 37u5395099N, 027u2393299E, 400 m a.s.l., on soil, 2 February . 2007, leg. M. Kırmacı MKIR 3820; PROV. AYDIN: I mamköy village, 37u5290.599N, 027u5492799E, 150 m, on soil, 6 February 2008, leg. M. Kırmacı and Emre Ağcagil EMA 97, conf. T.L. Blockeel (E). Five taxa were previously known in the genus Fossombronia Raddi in the bryophyte flora of Turkey (Kürschner & Erdağ, 2005; Ros et al., 2007), although F. foveolata Lindb. has been reported only by Smith (1990) without precise collection data or locality. The echinate spores (37240 mm in diameter) and the elaters with 223 spirals distinguish F. echinata from the other representatives of the genus in Turkey. The specimens were collected from two relatively close localities (nearly 40 km distant) on soil in clearings in destroyed Pinus brutia forest, maquis, and olive plantations. The conditions at each site are very similar because of the typical Eastern Mediterranean climate with long and dry summers and rainfall almost restricted to the spring and winter seasons. Accompanying species were Barbula unguiculata Hedw., Didymodon ferrugineus (Schimp. ex Besch.) M.O. Hill, Weissia long- ifolia Mitt., Trichostomum brachydontium Bruch, Bryum caespiticium Hedw., Bryum dichotomum Hedw., Cheilothela chloropus (Brid.) Broth., Microbryum starckeanum (Hedw.) R.H.Zander, Enthostodon durieui Mont., Phascum cuspidatum Schreb. ex Hedw. var. piliferum (Hedw.) Hook. & Taylor, Fissidens viridulus (Sw. ex anon.) Wahlenb., F. caespitiformis subsp. multispira (Schiffn.) J.R.Bray & D.C.Cargill, Riccia sorocarpa Bisch., R. beyrichiana Hampe ex. Lehm. and Petalophyllum ralfsii (Wilson) Nees & Gottsche. 11. Jubula hutchinsiae (Hook.) Dumort. subsp. javanica (Steph.) Verd. Contributors: Vadim A. Bakalin, Seungse Choi and Byung-Yun Sun Republic of Korea: JEONBUK PROVINCE: Muju-gun, Anseong-myeon, Deogyu Mt., Wolseong Stream, broadleaved forest, 35u4691399N, 127u4292299E, ca 680 m a.s.l., on wet rocks near stream, 2 April 2008, leg. S. Choi Kor-02-0408 (JNU, duplicate in VLA). This species is widely distributed in temperate and subtropical areas in the world, but in East Asia is mainly represented by subsp. javanica. The subspecies is found in the Caucasus (both Russian and Georgian parts), Asia Minor, the Himalayas, south-east Asia, Indo-Malaysia, the Philippines, Japan, Formosa, Samoa, Hawaii, Madagascar, Japan, Java and China (Duda, 1982; Guerke, 1978). This is the first record of the species for the Korean Peninsula and fills a gap between the Japanese islands and continental China. 12. Meesia hexasticha (Funck) Bruch Contributors: Ryszard Ochyra, Shiv Mohan Singh and Halina Bednarek-Ochyra Spitsbergen: Brøgger Halvøya on the southern side of Kongsfjorden in the north-western part of the island, Ny Ålesund, 78u55.0979N, 11u56.9679E, 17 m a.s.l, in wet situation in mossy tundra, August 2007, leg. Shiv Mohan Singh (KRAM). Meesia hexasticha is an Eurasian species having the main centre of its occurrence in Central Europe (Ochyra et al., 1988), where it is very rare and scattered and has not been rediscovered at many of its stations for over a century. Therefore it is considered to be an endangered species in Europe (Schumacker & Martiny, 1995). In addition, M. hexasticha is known in Fennoscandia (Söderström, 1998), but the record from Iceland (Frahm, 1975) is considered doubtful by Jóhannsson (1983) and the same author subsequently excluded the species from the Icelandic moss flora (Jóhannsson, 1995). Outside Europe, M. hexasticha is exceedingly rare in Yakutia and Chukotka in Arctic Siberia (Afonina, 2004; Ignatov, Afonina & Ignatova, 2006). The present discovery of M. hexasticha on Spitsbergen increases the moss flora of this arctic archipelago to 289 species (Frisvoll & Elvebakk, 1996) and represents the northernmost occurrence of this species. BRYOLOGICAL NOTES 13. Pleuridium nervosum (Hook.) Mitt. Contributors: Ryszard Ochyra and Halina BednarekOchyra Ethiopia: BALE MOUNTAINS: (1) Wasama, 6u559N, 39u469E, 920 m a.s.l, afroalpine Festuca–Pentaschistis grasslands on shallow and seasonally waterlogged soils overlying solid rock, with Kniphofia, 8u SW-facing rock ledge, pioneer moss on open silt, 10 January 1990, leg. Sabine & Georg Miehe 845 (KRAM); (2) Finchaya Habera, 7u009N, 39u449E, 3460 m a.s.l., afroalpine plant successions on mounds of the Giant Molerat and associated rodents (pioneer vegetation), on open silty ground, 31 December 1989, leg. Sabine & Georg Miehe 384 (KRAM). This Australasian-African species has long been known only from the southern Africa (Magill, 1981). Subsequently, it was recorded from Mt. Kenya (Townsend, 2005), but earlier it had been reported by Miehe & Miehe (1994) from the Bale Mountains in Ethiopia. Because no details of this record have been available, the relevant voucher collections are cited hereby. 57 species. The closely related P. saviana (De Not.) Latzel is also found in the summit region of Mt Kékes, the highest elevation of Hungary, and perhaps P. incurvata has been confused with that species in the field. The abovementioned specimen is the first confirmed record of the species for Hungary. 16. Ptychomnion densifolium (Brid.) A.Jaeger Contributors: Ryszard Ochyra, Marc Lebouvier and Halina Bednarek-Ochyra Île Amsterdam: Le Pignon, in a gully on a 10u SW-facing slope, 37u51939.699S, 77u32917.999E, 604 m a.s.l., continuous vegetation cover on saturated soil, 7 December 2007, leg. M. Lebouvier A081/1 (KRAM). A southern pan-temperate species, known from southern South America (Kühnemann & Gonçalves Carralves, 1975), New Zealand (Tangney & Fife, 1997), as well as some islands of the Southern Ocean, including Tristan da Cunha from where it was originally described as Hypnum densifolium (Bridel, 1812; Dixon, 1960), as well as subantarctic Maquarie Island (Seppelt, 2004), Marion Island (Zanten, 1971) and Îles Crozet (Ochyra, 2002), 14. Pohlia nutans (Hedw.) Lindb. subsp. schimperi (Müll.Hal.) Nyholm Contributor: Beáta Papp Hungary: ZEMPLÉN MTS: County of Borsod-AbaújZemplén, Kerek-kő peak at Háromhuta, 48u24937.799 N, 21u25939.199 E, ca 500 m a.s.l., in crevices of a vertical andesite rock, 27 May 2007, leg. B. Papp, conf. H. Köckinger, April 2008 (BP 175446). The distribution of Pohlia nutans subsp. schimperi was reevaluated recently by Köckinger, Kučera & Stebel (2005) on the basis of newly discovered localities in the Western Carpathians, the Sudetes, South Bohemia and in the eastern part of the Alps. Later, the moss was also reported from the western part of the Balkan mountain range, Stara Planina Mts, Serbia (Erzberger, 2007). The Hungarian occurrence in the foothills of Carpathians fits well in the known distribution. P. nutans subsp. schimperi is new to the Hungarian bryoflora (Erzberger & Papp, 2004). 15. Pseudoleskea incurvata (Hedw.) Loeske Contributor: Peter Erzberger Hungary: MÁTRA MTS: County of Heves, on andesite boulders in beech forest on the north side of the summit of Mt Kékes near Parád, ca 1000 m a.s.l. , 25 March 1951, leg. Á. Boros, as an admixture in a specimen of Grimmia hartmanii Schimp., det. P. Erzberger, April 2008 (BP 113128). The original label on the specimen reads: Dr. A. Boros: Plantae Hungariae exsiccatae Grimmia hartmanii Schpr. Comit. Heves. In saxis andesit. in faginetis sept. culminis montis Kékes prope Parád d. 25. marc. 1951 Alt. cca 1000 m.s.m. The occurrence of P. incurvata in Hungary was somewhat controversial. Although reported by Hungarian authorities (Boros, 1968; Orbán & Vajda, 1983), it was excluded in the recent checklist (Erzberger & Papp, 2004), because all available specimens were revised as other where it is fairly frequent and locally abundant (Ochyra, personal observations). The present discovery extends the known range of the species to the southern cool-temperate zone in the South Indian Ocean sector. 17. Racomitrium aciculare (Hedw.) Brid. Contributor: Peter Erzberger Hungary: BÖRZSÖNY MTS: County of Nógrád, on shaded rock of the hill Rakottyásbérc above the valley Bacsinavölgy near Királyháza, 23 May 1958, leg. L. Vajda, as an admixture in a specimen of Grimmia hartmanii Schimp., det. P. Erzberger, April 2008, conf. H. Bednarek-Ochyra, November 2008 (BP 59411, 175909). The original label on the specimen reads: Herbar. Musei Nat. Hungar. Budapest, Flora Hungarica, Grimmia hartmanii Schpr. Comit. Nógrád. In rupibus umbrosis montis Rakottyásbérc supra vallem Bacinavölgy prope Királyháza, montes Börzsöny. Racomitrium aciculare had been reported for Hungary by Düll (1985, 1992), but these reports were erroneous (Düll, in litt.; Erzberger & Papp, 2004). Boros and Vajda collected R. aquaticum (Brid. ex Schrad.) Brid. from several sites in the Börzsöny Mts (Boros, 1968), and these records were confirmed by Bednarek-Ochyra (2006). R. aquaticum is also found in the envelope together with R. aciculare, Grimmia hartmanii and Hypnum cupressiforme Hedw. R. aciculare is new to the bryoflora of Hungary, and this record completes the range of the species in the countries of the Carpathian mountains (Bednarek-Ochyra 2006). 18. Racomitrium lanuginosum (Hedw.) Brid. Contributors: Halina Bednarek-Ochyra, Marc Lebouvier and Ryszard Ochyra Île Amsterdam: Mont de la Dives (highest point of the island), 5u W-facing slope, 37u50955.799S, 77u32955.099E, 881m a.s.l., open vegetation in fell-field with the endemic grass Agrostis delislei and the endemic plantain Plantago 58 BRYOLOGICAL NOTES stauntoni, 28 November 2007, leg. M. Lebouvier A012/2 (KRAM). Racomitrium lanuginosum is a pan-Holantarctic species, occurring on all subantarctic islands from South Georgia to Macquarie Island, on the southernmost tips of South America, Africa and south-western Australia, and extending to the northern maritime Antarctic, as well as on Tristan da Cunha and Gough Island in the South Atlantic Ocean in the cool-temperate zone (Ochyra, Lewis Smith & Bednarek-Ochyra, 2008). The discovery of this species on Île Amsterdam was therefore expected and it nicely completes the continuous geographical range of the species in the Southern Ocean. It is very likely that the reports of R. pruinosum (Wilson) Müll.Hal. (Bescherelle, 1875; Schenck, 1905) from Îles Amsterdam refer to R. lanuginosum since this species is restricted to Australasia only (Vitt & Marsh, 1988), whereas its only record from southern South America is very doubtful. 19. Riccardia georgiensis (Steph.) Hässel subsp. sympodea R.M.Schust. Contributors: Jiřı́ Váňa, Ryszard Ochyra, Marc Lebouvier and Beata Cykowska Îles Kerguelen: GRANDE TERRE: Presqu’ı̂le Bouquet de la Grye: (1) in the vicinity of the hut in Port Couvreux, 49u17904.499S, 69u41935.499E, ca 20 m a.s.l., on wet ground concealed within patches of Breutelia integrifolia and Sanionia uncinata on stream banks, 19 November 2006, leg. R. Ochyra 356/06 (KRAM); (2) on the west shore of a large un-named lake in the central part of the peninsula 4 km west of Port Couvreux, 49u17909.55699S, 69u39901.37999E, ca 100 m a.s.l., intermixed with Willia calobolax in dry rocks crevices, 21 November 2006, leg. R. Ochyra 731/06 (KRAM). Previously Riccardia georgiensis subsp. sympodea has been recorded only from Marion Island in the Prince Edward Islands archipelago (Schuster, 1989) and Île de la Possession in the Îles Crozet archipelago (Grolle, 2002) in the Subantarctic, as well as from Livingston Island in the South Shetland Islands archipelago in the Antarctic (Bednarek-Ochyra et al. 2000). With the extension of its range to Îles Kerguelen, R. georgiensis subsp. sympodea is firmly established as an amphiatlantic subantarctic taxon. This is in contrast to the type subspecies which is an amphiatlantic temperate taxon, widespread in southern South America (Hässel de Menéndez, 1972) and on the Falkland Islands (Engel, 1990), and recently recorded also from Îles Kerguelen (Váňa & Gremmen, 2006). 20. Schistidium confusum H.H.Blom Contributors: Peter Erzberger and Wiebke Schröder Hungary: BUDA MTS: Budapest, on the hill ‘Sashegy’, 47u28958.899N, 19u01912.299E, ca 250 m a.s.l., on concrete joined to dolomite, 28 March 2008, leg. P. Erzberger 12896, det. W. Schröder, April 2008 (B). Schistidium confusum is not included in the checklist of Hungarian bryophytes (Erzberger & Papp, 2004), nor was it found during a revision of Schistidium specimens from BP by P.E. and W.S. (Erzberger & Schröder, 2008). Its occurrence in Hungary was, however, to be expected. The collection site within the confines of the capital of Hungary is an important nature reserve with many rare species of dolomitic rocky grasslands. Visitors are led on paths with small walls of concrete and dolomite in places, many of them colonized by species of Schistidium, e.g. S. crassipilum H.H.Blom, S. brunnescens Limpr. subsp. brunnescens, and S. dupretii (Thér.) W.A.Weber. 21. Schistidium praemorsum (Müll.Hal.) Herzog Contributors: Ryszard Ochyra, William R. Buck and Halina Bednarek-Ochyra Chile: XII REGIÓN, PROV. ANTÁRTICA CHILENA: Comuna Cabo de Hornos, Isla Navarino, Parque Etnobotánico Omora, ca 3 km west of Puerto Williams, 54u5692623199S,67u3895399267u3993699W, ca 52100 m a.s.l., on rock by stream in Nothofagus forest, 21 November 2001, leg. W. R. Buck 40759 (KRAM, NY). Although Schistidium praemorsum is a distinct and easily identifiable species in its almost entirely bistratose laminal cells in the upper part of the leaf, coarsely denticulate and terete leaf hair-point and reduced peristome teeth, it has been rarely collected in South America and in the maritime Antarctic (Ochyra, Bednarek-Ochyra & Lewis Smith, 2008). So far, the species is known on mainland South America only from high elevations in the Central Andes of Bolivia (Herzog, 1916) and north-western Argentina (Müller, 1882), as well as from western and southern Patagonia (Ochyra, Lewis Smith & Bednarek-Ochyra, 2008). Here, it is recorded for the first time from Chile and the archipelago of Tierra del Fuego in the southernmost tip of the continent. 22. Sematophyllum perrevolutum Broth. Contributor: C.C. Townsend Kenya: UASIN GISHU DISTRICT: roadside forest between Nakuru and Eldoret, ca 1 km past turning to Kisumu, on rotting log, 15 March 1977, leg. C.C. Townsend 77/41 (EA, Priv. Herb. Townsend); in another part of the same forest, also on a rotting log, leg. C.C.Townsend 77/42 (Priv. Herb. Townsend); ELGEYO DISTRICT: Cherangani Hills, Yemit, 0u599N, 35u27.59E, 8 km. N.W. of Cheptongei, on rotting log, 2500 m a.s.l., 6 February 1985, leg. C.C. Townsend 85/ 383 (Priv. Herb. Townsend); SOUTH NYERI DISTRICT: Aberdare Mts., on Erica stems above the S. side of Chania Falls, 0u279S, 36u449E, ca 3030 m a.s.l., 8 April 1975, leg. C.C. Townsend 75/877 (Priv. Herb. Townsend). The leaves in this attractive little moss are very concave, sometimes very deeply so centrally, so that the ends of the concavity meet a little below the apex and a little above the base, and a broad flat marginal band is formed round the concavity rather than a narrower recurved one. In this and other characters the first two specimens are a very good match for Dummer 522 from forest, Kipaya, Uganda, in Herb. Dixon (BM). The third specimen appears unhappy and brownish, probably affected by formic acid from the 59 BRYOLOGICAL NOTES abundant ants in the log, but otherwise appears to share the characters of the other two very convincingly. 23. Splachnobryum obtusum (Brid.) Müll.Hal. Contributor: C.C. Townsend Zambia: LUSAKA DISTRICT: on damp clay soil in a dambo between the Great North Road and Kamaila Forest Reserve, E. of the Road ca 36 km N. of Lusaka, 1250 m a.s.l., leg. C.C. Townsend 75/12, 9 February 1975 (Priv. Herb. C.C. Townsend). 24. Taxifolium taxirameum (Mitt.) M.Fleisch. Contributor: C.C. Townsend Kenya: NAKURU DISTRICT: earthy bank by the dried-up river below Makalia Falls, Lake Nakuru National Park, 0u249S, 36u059E, 1760 m a.s.l., 1 April 1977, leg. C.C. Townsend 77/338 (Priv. Herb. Townsend). This species, which I often encountered in India, Ceylon and Nepal, varies a good deal in the prominence of the papillae at the upper end of the leaf cells, and in the present gathering they are small but clearly visible. 25. Tetralophozia filiformis (Steph.) Urmi Contributors: Vadim A. Bakalin, Seungse Choi and Byung-Yun Sun Republic of Korea: JEONBUK PROVINCE: Muju-gun, Anseong-myeon, Deogyu Mt., southern macroslope, Deokgok Stream, broad-leaved forest with admixture of Pinus densiflora Siebold and Zucc., 35u5195199N, 127u4391599E, 723 m a.s.l., on shady cliffs near stream, 1 July 2008, leg. V.A. Bakalin & S. Choi Kor-01-07-08 (JNU, duplicate in VLA). The distribution of Tetralophozia filiformis was summarised by Urmi (1983) and Konstantinova (2002). The species was recently also recorded for Eastern Siberia by Bakalin (2004). At present it is known in Europe (Spain), Asia (Siberia, Japan, Taiwan, southern China, Nepal, India, Butan, Malaysia) and Northern America (British Columbia). This record is the first for the Korean Peninsula. The species has a disjunctive temperate montane distribution and is rare worldwide. The first author (VAB) carefully searched many mountain systems for this species in south Siberia and the Russian Far East, but collected it only twice (including the present record). On the Deogyu mountain the authors studied many similar cliffs along streams in the same communities, but discovered the species only once. The probable reason for this is low reproductive activity in T. filiformis, and like some Herbertus species it has a relict distribution everywhere at the present time. 26. Weissia breutelii Müll.Hal Contributor: Özlem Tonguç Yayintaş Turkey, HATAY: Tekepinari Village, Karapinar Valley, Musa Mount, 510 m a.s.l., on soil, 15 May 2001, leg. Özlem Tonguç Yayintaş T 1234, conf. R.H. Zander (MO, Çanakkale Onsekiz Mart University herbarium). Weisia breutelii has a disjunct distribution between the Americas and S.W. Asia. It is well known as a Caribbean and Central American species (Britton, 1915; Reese, 1991; Zander, 1993; Allen, 2002), extending to Brazil (Yano, 1996) and north-eastern and north-western South America (Heyn & Herrnstadt, 2004). In S.W. Asia it occurs in Israel (Herrnstadt et al., 1982; Frey & Kürschner, 1991), this being the nearest locality to the new Turkish site. This geographical disjunction seems rather puzzling. Frey and Kürschner (1983) indicated that such disjunctions might be explained by Circum-Tethyan distributions, and our sample collection area is situated in the West Irano-Turanian province. ACKNOWLEDGEMENTS H. Bednarek-Ochyra and R. Ochyra have gained financial support from the Polish Ministry of Science and Higher Education through grants No. N 303 063 32/2264 for H. Bednarek-Ochyra and No. 2 P04G 043 29 for R. Ochyra. The field work of R. Ochyra on Îles Kerguelen was organised by Marc Lebouvier, Paimpont, within the programme 136 ECOBIO of the French Polar Institute (IPEV) and his facilities are gratefully acknowledged. The contributions to the flora of Îles Kerguelen and Île Amsterdam have been prepared under the auspices of the SCAR programme Evolution and Biodiversity in the Antarctic (EBA). A. . Erdağ and H. Kürschner are grateful to TUBI TAK (CAYDAG-105Y016) for supporting A. Erdağ’s field studies in Kemaliye. P. Erzberger wishes to thank E. Maier for kindly examining the specimen of Coscinodon cribrosus, and H. Bednarek-Ochyra for helpful comments and examination of the specimen of Racomitrium aciculare. B. Papp is grateful to H. Köckinger for confirming the identity of Pohlia nutans subsp. schimperi. J. Váňa has received financial support for his research from the Ministry of Education of the Government of the Czech Republic through grant No. 0021620828. Özlem Tonguç Yayintaş gives special thanks to Dr R.H. Zander for confirming the determination of Weissia breutelii and linguistic assistance; he is also very grateful to the curator at Missouri Botanical Garden for access to herbarium specimens for comparison, and to the director of Missouri Botanical Garden for making the moss herbarium available for this study. TAXONOMIC ADDITIONS AND CHANGES: Nil. REFERENCES Afonina OM. 2004. Conspectus of the moss flora of Chukotka. Sankt Petersburg: Botanicheskiy Institut im. Komarova, Rossiyskaya Akademia Nauk (in Russian). Aleffi M, Sabovljević M, Tacchi R. 2003. Didymodon sicculus M.J.Cano, Ros, Garcia-Zamora & J.Guerra (Pottiaceae, Musci), new to Italy. Cryptogamie, Bryologie 24: 49251. Allen B. 2002. Moss Flora of Central America. Part 2. Encalyptaceae – Orthotrichaceae. Missouri: Missouri Botanical Garden Press. Arnell SW. 1952. Hepaticae collected in South and West Africa 1951. New and little known species. Botaniska Notiser 1952: 3072329. Arnell SW. 1953. List of Hepaticae collected in Marion Island by Mr. R. W. Rand Dec. 1951 2 April 1952. Svensk Botanisk Tidskrift 47: 4112425. Bakalin VA. 2004. The liverworts of Stanovoye Nagorye Upplands. Arctoa 13: 73283. 60 BRYOLOGICAL NOTES Bednarek-Ochyra H. 2006. A taxonomic monograph of the moss genus Codriophorus P. Beauv. (Grimmiaceae). Kraków: W. Szafer Institute of Botany, Polish Academy of Sciences. Bednarek-Ochyra H, Matteri CM, Ochyra R. 1996. A major range extension of Racomitrium lamprocarpum (Musci, Grimmiaceae) in South America. Fragmenta Floristica et Geobotanica 41: 995–1000. Bednarek-Ochyra H, Ochyra R. 1994. Racomitrium lamprocarpum (Musci, Grimmiaceae) in southern South America. Fragmenta Floristica et Geobotanica 39: 361–367. Bednarek-Ochyra H, Ochyra R, Soldán Z. 2002. Racomitrium lamprocarpum [in Ecuador]. In: TL Blockeel, ed. New national and regional bryophyte records, 5. Journal of Bryology 24: 90. Bednarek-Ochyra H, Váňa J, Ochyra R, Lewis Smith RI. 2000. The liverwort flora of Antarctica. Cracow: Polish Academy of Sciences, Institute of Botany. Bescherelle E. 1875. Note sur les mousses des ı̂les Saint-Paule et d’Amsterdam. Comptes Rendus Hebdomadaires des Séances de l’Académie des Sciences 81: 7202725. Blockeel TL, Ros RM, Sabovljević M, Cano MJ, Gallego MT, Muñoz J. 2002. New and interesting bryophyte records for Greece. Cryptogamie, Bryologie 23: 149–155. Boros Á. 1968. Bryogeographie und Bryoflora Ungarns. Budapest: Akadémiai Kiadó. Bridel SE. 1812. Muscologiae recentiorum supplementum seu species muscorum. Pars II. Gothae: ex Officina Libraria Ettingeriana. Britton EG. 1915. West Indian Mosses-II. Mosses of Danish West Indies and Virgin Islands. Bulletin of the Torrey Botanical Club 42: 128. Cano MJ, Gallego MT, Garilleti R, Juaristi R, Lara F, MartinezAbaigar J, Mazimpaka V, Rosello JA, Sanchez-Moya MC, Uridoz A. 2001. Aportaciones al conocimiento de la flora briologica Espanola. Notula XIII: Hepaticas y musgos de Mallorca (Islas Baleares). Boletin de la Sociedad Espanola de Briologia 18/19: 1032110. Cano MJ, Ros RM, Garcia-Zamora P, Guerra J. 1996. Didymodon sicculus sp. nov. (Bryopsida, Pottiaceae) from the Iberian Peninsula. Bryologist 99: 401–406. Casas C. 1991. New checklist of Spanish mosses. Orsis 6: 3226. Çetin B, Uyar G. 2004. A new check-list of the mosses of Turkey. Journal of Bryology 26: 2032220. Churchill SP, Griffin D III, Muñoz J. 2000. A checklist of the mosses of the tropical Andean countries. Ruizia 17: 1–203. Cortini Pedrotii C. 2001. New checklist of the mosses of Italy. Flora Mediterranea 11: 23–107. Cvetić T, Sabovljević M. 2004. New and interesting bryophyte records for Montenegro. Phytologia Balcanica 10: 67269. Deguchi H. 1987. Studies on some Peruvian species of the Grimmiaceae (Musci, Bryophyta). In: Inoue H, ed. Studies on cryptogams in southern Peru. Tokyo: Tokai University Press, pp. 19–74. Dixon HN. 1960. Mosses of Tristan da Cunha. In: Christophersen E, ed. Results of the Norwegian Scientific Expedition to Tristan da Cunha 1937–1938. No. 48. Oslo: Kommissjon hos H. Aschehoug & Co. (W. Nygaard), pp. 1–49. Duda J. 1982. Ad distributionem Hepaticarum in Caucaso notula. Novosti Sistematiki Nizshikh Rasteniy 19: 200–204. Düll R. 1985. Distribution of the European and Macaronesian Mosses (Bryophytina) Part II. Bryologische Beiträge 5: 110–232. Düll R. 1992. Distribution of the European and Macaronesian Mosses (Bryophytina) Annotations and Progress. Bryologische Beiträge 8/ 9: 1–223. Engel JJ. 1990. Falkland Islands (Islas Malvinas). Hepaticae and Anthocerotophyta: a taxonomic and phytogeographic study. Fieldiana Botany, New Series 25: 1–209. Erzberger P, 2007. Pohlia nutans subsp. schimperi [in Serbia]. In: Blockeel TL, ed. New national and regional bryophyte records, 15. Journal of Bryology 29: 141. Erzberger P, Papp B. 2004. Annotated checklist of Hungarian bryophytes. Studia Botanica Hungarica 35: 912149. Erzberger P, Schröder W. 2008. The genus Schistidium (Grimmiaceae, Musci) in Hungary. Studia Botanica Hungarica 39: 27288. Fojcik B, Gumieniak A. 1999. A locality for Campylopus introflexus (Musci, Dicranaceae) in Płaskowyż Kolbuszowski (Kotlina Sandomierska). Fragmenta Floristica et Geobotanica Series Polonica 6: 288–290. Frahm J.-P. 1975. Beiträge zur Moosflora von Island. Herzogia 3: 1712188. Frey W, Kürschner H. 1983. New records of bryophytes from Transjordan with remarks on phytogeography and endemism in SW Asiatic mosses. Lindbergia 9: 1212132. Frey W, Kürschner H. 1991. Conceptus Bryophytorum Orientalum et Arabicorum: An Annotated Catalogue of the Bryophytes of Southwest Asia. Bryophytorum Bibliotheca, Band 39. BerlinStuttgard: J.Cramer. Frey W, Frahm J.-P, Fischer E, Lobin W. 2006. The liverworts, mosses and ferns of Europe. English edition revised and edited by T.L. Blockeel. Colchester: Harley Books. Frisvoll AA, Elvebakk A. 1996. Part 2. Bryophytes. In: Elvebakk A, Prestrud P, eds. A catalogue of Svalbard plants, fungi, algae and cyanobacteria. Norsk Polarinstitutt Skrifter 198: 57–172. Fröhlich, J. 1959. Bryophyten aus Vorderasien. Annalen des Naturhistorischen Museums Wien 63: 31232. Grims F. 1999. Die Laubmoose Österreichs. Catalogus Florae Austriae. II. Teil, Bryophyten (Moose), Heft 1, Musci (Laubmoose). Biosystematics and Ecology Series 15: 1–418. Grolle R. 1971. Hepaticopsida. In: Zinderen Bakker EM van Sr, Winterbottom JM, Dyer RA, eds. Marion and Prince Edward Islands. Report on the South African Biological and Geological Expedition 1965–1966. Cape Town: A.A. Balkema, pp. 173–227. Grolle R. 2002. The Hepaticae and Anthocerotae of the subantarctic and temperate islands in the eastern Southern Hemisphere (90uE to 0u): an annotated catalogue. Journal of Bryology 24: 57280. Guerke WR. 1978. A monograph of the genus Jubula Dumortier. Bryophytorum Bibliotheca, Band 17. Berlin/Stuttgard: J.Cramer. Hässel de Menéndez GG. 1972. Revision taxonomica del genero ‘Riccardia’ (Hepaticae). Revista del Museo Argentino de Ciencias Naturales ‘Bernardino Rivadavia’, Botánica 4: 12242. Herrnstadt I, Heyn CC, Ben-Sasson R, Crosby MR. 1982. New records of mosses from Israel. Bryologist 85: 2142217. Herzog T. 1916. Die Bryophyten meiner zweiten Reise durch Bolivia. Bibliotheca Botanica 87: 1–347. Heyn CC, Herrnstadt I. 2004. The bryophyte flora of Israel and adjacent regions. Jerusalem: The Israel Academy of Science and Humanities. Holotová E, Šoltés R. 1997. Campylopus introflexus new moss species to the Slovakian moss flora. Biologia (Bratislava) 52: 494. Ignatov MS, Afonina OM, Ignatova EA. 2006. Check-list of mosses of East Europe and North Asia. Arctoa 15: 12130. Jiménez JA, Ros RM, Cano MJ, Guerra J. 2004. New distribution data on Didymodon anserinocapitatus (X.J.Li) R.H. Zander, D. maschalogena (Renauld & Cardot) Broth. and D. sicculus M.J. Cano et al. (Bryophyta, Pottiaceae). Cryptogamie, Bryologie 25: 91297. Jóhannsson B. 1983. A list of Icelandic bryophyte species. Acta Naturalia Islandica 30: 1229. Jóhannsson B. 1991. Icelandic bryophytes. Dicranaceae. Fjölrit Náttúrufræðistofnunar 19: 1–119. Jóhannsson B. 1995. Icelandic bryophytes. Mniaceae, Aulacomniaceae, Meesiaceae, Catoscopiaceae, Bartramiaceae and Timmiaceae. Fjölrit Náttúrufræðistofnunar 26: 1–129. Köckinger H, Kučera J, Stebel A. 2005. Pohlia nutans subsp. schimperi (Müll.Hal.) Nyholm, a neglected Nordic moss in Central Europe. Journal of Bryology 27: 3512355. Konstantinova NA. 2002. The genus Tetralophozia (R.M. Schust.) Schljakov (Lophoziaceae, Hepaticae) in Russia. Arctoa 11: 45252. Kučera J, Váňa J. 2003. Check- and Red List of bryophytes of the Czech Republic. Preslia 75: 1932222. BRYOLOGICAL NOTES Kühnemann O, Gonçalves Carralves MF. 1975. Monografia preliminar para la flora criptogámica fuegina: los musgos de la familia Ptychomniaceae (Bryophyta). Darwiniana 19: 583–617. Kürschner H. 2008. A key to the acrocarpous mosses (Bryophytina p.p., excl. Pottiaceae) of the Near and Middle East. Towards a bryophyte flora of the Near and Middle East, 7. Nova Hedwigia 86: 432103. Kürschner H, Erdağ E. 2005. Bryophytes of Turkey: an annotated reference list of the species with synonyms from the recent literature and an annotated list of Turkish bryological literature. Turkish Journal of Botany 29: 952154. Magill RE. 1981. Flora of southern Africa. Bryophyta. Part 1. Mosses. Fascicle 1. Sphagnaceaeae2Grimmiaceae. Pretoria: Botanical Research Institute. Menzel M. 1986. Beitrag zur andinen Laubmoosflora von Peru. Willdenowia 15: 5292555. Miehe G, Miehe S. 1994. Ericaceous forest and heathlands in the Bale Mountains of South Ethiopia. Ecology and man’s impact. Hamburg: Stiftung Walderhaltung in Africa and Bundesforschungsanstalt für Forst- und Holzwirtschaft. Mikulášková E. 2006. Development in distribution of the neophytic moss Campylopus introflexus in the Czech Republic. Bryonora 38: 126. Müller C. 1882. Prodromus bryologiae argentinicae II, seu Musci lorentziani argentinici. Linnaea 43: 341–486. Ochyra R. 2002. Ptychomnion ringianum Broth. & Kaal., synonymous with P. densifolium (Brid.) A.Jaeger (Ptychomniaceae). Journal of Bryology 24: 87288. Ochyra R, Bednarek-Ochyra H, Lewis Smith RI. 2008. New and rare moss species from the Antarctic. Nova Hedwigia 87: 4572477. Ochyra R, Lewis Smith RI, Bednarek-Ochyra H. 2008. The illustrated moss flora of Antarctica. Cambridge: Cambridge University Press. Ochyra R, Sérgio C, Schumacker R. 1988. Racomitrium lamprocarpum (C. Muell.) Jaeg., an austral moss disjunct in Portugal, with taxonomic and phytogeographic notes. Bulletin du Jardin Botanique National de Belgique 58: 225–258. Ochyra R, Szmajda P, Bednarek H, Bocheński W. 1988. M. 387. Meesia hexasticha (Funck) Bruch. In: Tobolewski Z, Wojterski T, eds. Atlas of the geographical distribution of spore plants in Poland. Series V. Mosses (Musci). 3. Warszawa 2 Poznań: Państwowe Wydawnictwo Naukowe, pp. 53–61 z map. Orbán S, Vajda, L. 1983. Magyarország mohaflórájának kézikönyve. Budapest: Akadémiai Kiadó. Papp B., Sabovljević M. 2003. Contribution to the bryophyte flora of Turkish Thrace. Studia Botanica Hungarica 34: 43254. Puglisi M, Privitera M, Prezzavento AD. 2004. More about occurence of Didymodon sicculus Cano, Ros, Garcia-Zamora & Guerra (Musci, Pottiaceae) in Italy. Braun-Blanquetia 34: 47249. Razgulyaeva LV, Napreenko MG, Wolfram Ch, Ignatov MS. 2001. Campylopus introflexus (Dicranaceae, Musci) – an addition to the moss flora of Russia. Arctoa 10: 185–188. Reese WD. 1991. Weissia (Hymenostomum) flavescens new to the United States. Bryologist 94: 1792180. Ros RM, Mazimpaka V, Abou-Salama U, Aleffi M, Blockeel TL, Brugués M, Cano MJ, Cros RM, Dia MG, Dirkse GM, El Saadawi W, Erdağ A, Ganeva A, González-Mancebo JM, Herrnstadt I, Khalil K, Kürschner H, Lanfranco E, Losada-Lima A, Refai MS, Rodrı́guez-Nuñez S, Sabovljević M, Sérgio C, Shabbara H, Sim-Sim M, Söderström L. 2007. Hepatics and Anthocerotes of the 61 Mediterranean, an annotated checklist. Cryptogamie Bryologie 28: 351–437. Sabovljević M, Tsakiri E, Sabovljević A. 2008. Towards the bryophyte flora of Greece, studies in Chalkidiki area (North Greece). Cryptogamie, Bryologie 29: 1432155. Schenck H. 1905. Ueber Flora und Vegetation von St. Paul und NeuAmsterdam. In: Chun C, ed. Wissenschaftliche Ergebnisse der Deutschen Tiefsee-Expedition Valdivia 189821899. 2(1). Jena: Verlag von Gustav Fischer, pp. 1792224. Schumacker R, Martiny P. 1995. Red Data Book of European bryophytes. Part 2. Threatened bryophytes in Europe including Macaronesia. In: European Committee for Conservation of Bryophytes. Red Data Book of European Bryophytes. Trondheim: ECCB, pp. 292193. Schuster RM. 1989. Studies on the hepatic flora of the Prince Edward Islands. I. Aneuraceae. Journal of the Hattori Botanical Laboratory 67: 592108. Seppelt RD. 2004. The moss flora of Macquarie Island. Kingston: Australian Antarctic Division. Smith AJE. 1990. The liverworts of Britain and Ireland. Cambridge: Cambridge University Press. Söderström L (ed). 1998. Preliminary distribution maps of bryophytes in northwestern Europe. 3. Musci (J–Z). Trondheim: Mossornas Vänner. Stebel A. 1995. Campylopus introflexus (Musci, Dicranaceae) found in the Carpathians. Fragmenta Floristica et Geobotanica 40: 909–911. Szűcs P, Erzberger P. 2007. Campylopus introflexus [in Hungary]. In: Blockeel TL, ed. New national and regional bryophyte records, 16. Journal of Bryology 29: 199. Tangney RS, Fife AJ. 1997. The occurrence of Ptychomnion densifolium in New Zealand. Journal of Bryology 19: 819–825. Townsend CC. 2005. Pleuridium nervosum [in Kenya]. In: Blockeel TL, ed. New national and regional bryolophyte records, 11. Journal of Bryology 27: 166. Townsend CC. 2007. Drepanocladus aduncus [in Tanzania]. In: Blockeel TL, ed. New national and regional bryophyte records, 17. Journal of Bryology 29: 278. Urmi E. 1983. Tetralophozia filiformis (Steph.) comb. nov. in Europe. Journal of Bryology 12: 3932401. Váňa J. 1985. Notes on some African hepatic genera 629. Folia Geobotanica et Phytotaxonomica 20: 81299. Váňa J, Gremmen N. 2006. Checklist of the hepatic flora of subAntarctic Îles Kerguelen. Cryptogamie, Bryologie 27: 1312139. Vitt DH, Marsh C. 1988. Population variation and phytogeography of Racomitrium lanuginosum and R. pruinosum. In: Engel JJ, Hattori S, eds, Bryological contributions presented in celebration of the distinguished scholarship of Rudolf M. Schuster. Beihefte zur Nova Hedwigia 90: 235–260. Yano O. 1996. A checklist of Brazilian bryophytes. Boletim do Instituto de Botanica (São Paulo) 10: 47–232. Yarcı C. 2000. Demirköy (Istranca Daglari / Trakya Bölgesi) ve Civarinin Orman Vejetasyonu. Ekoloji Dergisi 9: 13–18. Zander RH. 1993. Genera of the Pottiaceae: mosses of harsh environments. Bulletin of the Buffalo Society of Natural Sciences 32: 1–378. Zanten BO van. 1971. Musci. In: Zinderen Bakker EM van Sr, Winterbottom JM, Dyer RA, eds. Marion and Prince Edward Islands. Report on the South African Biological and Geological Expedition 1965–1966. Cape Town: A. A. Balkema, pp. 173–227. T.L. BLOCKEEL1, 9 Ashfurlong Close, Dore, Sheffield S17 3NN, UK. E-mail: Tblockeel@aol.com V. A. BAKALIN, Institute of Biology and Soil Science, Stoletiya Vladivostoka Street., 159, Vladivostok, Russia. E-mail: v_bak@list.ru H. BEDNAREK-OCHYRA & R. OCHYRA, Laboratory of Bryology, Institute of Botany, Polish Academy of Sciences, ul. Lubicz 46, 31-512 Kraków, Poland. E-mails: Halina.Bednarek@ib-pan.krakow.pl and Ryszard.Ochyra@ib-pan.krakow.pl W. R. BUCK, The New York Botanical Garden, Institute of Systematic Botany, Bronx, NY 10458-5126, USA. E-mail: BBUCK@nybg.org S. CHOI, Faculty of Biological Sciences, Chonbuk National University, Jeonju, Jeonbuk, Korea. E-mail: hepaticae@chonbuk.ac.kr 62 BRYOLOGICAL NOTES B. CYKOWSKA, Laboratory of Bryology, Institute of Botany, Polish Academy of Sciences, ul. Lubicz 46, 31-512 Kraków, Poland. E-mail: ibcykowska@ib-pan.krakow.pl A. ERDAĞ, Adnan Menderes Üniversitesi, Fen Edebiyat Fakültesi, Biyoloji Bölümü, 09010 Kepez-Aydın, Turkey P. ERZBERGER, Belziger Str. 37, D-10823 Berlin, Germany. E-mail: erzberger@erzfisch.de M. KIRMACI, Adnan Menderes Üniversitesi, Fen Edebiyat Fakültesi, Biyoloji Bölümü, 09010 Kepez- Aydın, Turkey H. KÜRSCHNER, Freie Universität Berlin, Institut für Biologie, Systematische Botanik und Pflanzengeographie, Altensteinstr. 6, D-14195 Berlin, Germany M. LEBOUVIER, CNRS UMR 6553, Université de Rennes 1, Station Biologique, F-35380 Paimpont, France. E-mail: marc.lebouvier@ univ-rennes1.fr B. PAPP, Hungarian Natural History Museum, Budapest, Pf. 222, H-1476, Hungary MARKO SABOVLJEVIĆ and ANETA SABOVLJEVIĆ, Institute of Botany and Garden Faculty of Biology, University of Belgrade Takovska 43, 11000 Belgrade Serbia. E-mail: sabmar@hotmail.com W. SCHRÖDER, Ludwigsstädter Str. 51, D-96337 Ludwigsstadt, Germany S. M. SINGH, National Centre for Antarctic & Ocean Research, Ministry of Earth Sciences, Government of India, Headland Sada, Vascoda-Gama, Goa - 403 804, India. E-mail: drsmsingh@yahoo.com B.-Y. SUN, Faculty of Biological Sciences, Chonbuk National University, Jeonju, Jeonbuk, Korea. E-mail: sunby@chonbuk.ac.kr C.C. TOWNSEND, 392 Staines Road, Twickenham, Middlesex TW2 5JA, UK. E-mail: cliff.townsend@blueyonder.co.uk J. VÁŇA, Department of Botany, Charles University, Faculty of Science, Benátská 2, CZ-128 01 Praha 2, Czech Republic. E-mail: vana@natur.cuni.cz ÖZLEM TONGUç YAYINTAŞ, Canakkale Onsekiz Mart University, Biga Vocational College, Technical Program, 17200, Biga, CanakkaleTurkey. E-mail: ozlemyayintas@hotmail.com Column editor, to whom contributions should be sent. 1