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27 March 2015 Euro Med-Checklist Notulae, 4
Author Affiliations +
Abstract

This is the fourth of a series of miscellaneous contributions, by various authors, where hitherto unpublished data relevant to both the Med-Checklist and the Euro Med (or Sisyphus) projects are presented. This instalment deals with the families Amaranthaceae, Asclepiadaceae, Boraginaceae, Caryophyllaceae, Compositae, Cruciferae, Euphorbiaceae, Guttiferae, Malvaceae, Onagraceae, Orobanchaceae, Portulacaceae, Rosaceae; Commelinaceae, Gramineae, Liliaceae and Palmae. It includes new country and area records, taxonomic and distributional considerations for taxa in Amaranthus, Cardamine, Cerastium, Commelina, Euphorbia, Hieracium, Hypericum, Lilium, Melinis, Myosotis, Oenothera, Orobanche, Portulaca, Pyrus, Rubus, Senecio, Silene, Sporobolus, Tulipa, Vincetoxicum and Washingtonia, the validation of names in Malva and Polycarpon, and a corrigendum to an entry for Pilosella in the previous instalment.

Notice

A succinct description of the Euro+Med project, with a list of recognized territories and their abbreviations, and the conventions used to indicate the status and presence of taxa, can be found in the introduction to the first instalment of the Euro+Med Notulae (Greuter & Raab-Straube 2005: 223–226) and on the Euro+Med PlantBase website (Euro+Med 2006+). For the previous instalment of the Euro+Med-Checklist Notulae, see Raab-Straube & Raus (2014).

The following have contributed entries to the present instalment: N. M. G. Ardenghi, Z. Barina, F. Bartolucci, P. Cauzzi, A. Danin, M. D'Antraccoli, E. Del Guacchio, G. Faggi, G. Galasso, D. Iamonico, A. V. Ivanova, G. Király, L. Peruzzi, D. Pifkó, E. von Raab-Straube, Th. Raus, L. Saéz, F. Sales, A. Sani, S. A. Senator, A. Strid, K. Sutorý, J.-M. Tison, V. M. Vasjukov, P. Verloove & E. Willing.

Amaranthaceae

  • Amaranthus palmeri S. Watson

    A It: Italy, Emilia-Romagna: Province of Ravenna, Cervia, via Romea Nord (SS16), 44°16′5.8″N, 12°19′40.4″E, near sea-level, road embankment with ruderal vegetation, 8 Oct 2014, Faggi, Iamonico & Ardenghi (HFLA). — As part of the forthcoming treatment of Amaranthaceae in the Euro+Med PlantBase project, recent field surveys in N Italy (Emilia-Romagna region) allowed us to find a population of dioecious amaranths belonging to Arnaranthus subg. Acnida (L.) Aellen ex K. R. Robertson (see Mosyakin & Robertson 1996). The flora of Italy currently includes two taxa belonging to A. subg. Acnida: A. tuberculatus (Moq.) J. D. Sauer (= A. rudis J. D. Sauer), and A. tamariscinus Nutt. (see, e.g., Iamonico 2010a). These two species belong to A. sect. Acnida (L.) Mosyakin & K. R. Robertson, which includes taxa without or with 1 or 2 tepals in the pistillate flowers, and mostly indehiscent fruits. By contrast, the newly discovered plants have 5 tepals and usually dehiscent fruits, features that characterize A. sect. Saueranthus Mosyakin & K. R. Robertson (see Mosyakin & Robertson 1996). Among the four species currently included in A. sect. Saueran thus (A. arenicola I. M. Johnst., A. greggii S. Watson, A. palmeri, A. watsonii Standl.), the Italian population can be certainly ascribed to A. palmeri, featuring glabrous or slightly pubescent (and not glandular) stems, spiny tipped bracts much longer than the tepals, and dehiscent fruits (see Mosyakin & Robertson 2003). Amaranthus palmeri is native to North America, currently known as alien in some European countries, especially in C Europe. As no previous records have been mentioned in Italian standard floras (see, e.g., Conti & al. 2005, 2007; Celesti-Grapow & al. 2010 and literature therein), this taxon is regarded as a new casual for Italy.

    D. Iamonico, N. M. G. Ardenghi & G. Faggi

Asclepiadaceae

  • Vincetoxicum mugodsharicum Pobed. — Fig. 1.

    + Rf(E): Russia, Samara province: Kinel district, near village Chubovka, 53°42′N, 50°58′E, 125 m. steppe slopes on red marly clay, 25 May 2014, Ivanova & Senator; ibid.: Pohvistnevo district, near village Staropohvistnevo, mountain Kopeika, 53°68′N, 52°16′E, 135 m, steppe slopes on red marly clay, 5 Jun 2014, Vasjukov & Ivanova (all LE, PVB; det. Vasjukov). — New species for the flora of Europe; previously found only in the Mugojar mountains in Kazakhstan (Pobedimova 1952) and in Russia in the S of the Orenburg region: Sol-Iletsk district, near village Trinity, and Perevolotsky district, Kuvayskaya steppe (Rjabinina & Knjazev 2009, as Vincetoxicum intermedium Taliev s.l.; Vasjukov & al. 2014). On the mountain Kopeika, V. mugodsharicum grows together with several rare species, such as Astragalus zingeri Korsh., Crambe aspera M. Bieb., Iris pumila L., Koeleria sclerophylla P. A. Smirn., Oxytropis knjazevii Vasjukov, Stipa korshinskyi Roshev., Thymus bashkiriensis Klokov & Des.-Shost., T. pseudopannonicus Klokov, T. punctulosus Klokov, T. talijevii Klokov & Des.-Shost., Trinia muricata Godet and Tulipa scythica Klokov & Zoz.

    V. M. Vasjukov, A. V. Ivanova & S. A. Senator

Boraginaceae

  • Myosotis discolor subsp. dubia (Arrond.) Blaise

    Bl: Valdés (2012) listed this taxon for Mallorca and Menorca based on bibliographic references unsubstantiated by herbarium specimens. In fact, the basis for these Balearic records is not known for certain. I have tried to find Balearic material of this species in several herbaria (BC, BCN, COI, HJBS, JACA, MA, MPU, VAL and herb. Universitat Illes Balears) without success, and do not believe that this species occurs in the Balearic Islands. L. Sáez

  • Myosotis ramosissima Rochel subsp. ramosissima

    + Bl(M): Mallorca: Escorca, Puig Major, 39°48′32″N. 2°47′53″E, 1350 m, rocky limestone slopes with Hypericum balearicum L. scrub, 3 Jun 2013, Sáez LS-7404 (herb. Sáez, BCB). — In recent floras (Bolòs & Vigo 1996; Valdés 2012) this species is not listed for the Balearic archipelago.

    L. Sáez

Caryophyllaceae

  • Cerastium arvense L. subsp. arvense

    Bl: This species was erroneously recorded from Mallorca (“ad rupes montis Puig-Major”) by Cambessèdes (1827, sub Cerastium strictum L.). The voucher specimen (Mallorca: ad apicem montis Puig Major, 21 Apr 1825, [Cambessèdes], MPU-Knoche) represents Arenaria grandiflora subsp. glabrescens (Willk.) G. López & Nieto Fel. L. Sáez

  • Polycarpon tetraphyllum subsp. dunense (P. Fraga & Rosselló) Iamonico, comb. & stat. nov.Polycarpon dimense P. Fraga & Rosselló in Flora Montiber. 47: 30. 2011. — Holotype: Spain, Menorca, in arenosis loco dicto Arenal de sa Cavalleria ad 10 m, 31 Mar 1996, Fraga (VAL).

    A recent molecular investigation by Kool & al. (2007) has shown that the genus Polycarpon L. is polyphyletic. Three phylogenetic lineages can be highlighted: the aggregate P. coquimbense Gereau & Martic. / P. suffruticosum Griseb. (from South America); P. prostratum (Forssk.) Asch. & Schweinf. (widespread in the tropics); and the “Polycarpon tetraphyllum clade” (mainly Mediterranean). The species P. coquimbense, P. suffruticosum and P. prostratum have to be excluded from Polycarpon, while the remaining members represent a polyploid complex. Kool & al. (2007) also suggested to treat all the members of the P. tetraphyllum (L.) L. group as a single species with several infraspecific taxa. Accordingly, new nomenclatural combinations were proposed also considering morphological, ecological, and chorological data (see, e.g., Iamonico 2013, 2015; Iamonico & Domina 2015).

    Polycarpon dunense was recently described by Fraga & Rosselló (2011) from mobile sand dunes on the N coast of Menorca (Balearic Islands). Although Kool & al. (2007) did not include this taxon in their phylogenetic analyses, there is no doubt that P. dunense belongs to the P. tetraphyllum group on the basis of its morphology. The species includes small annual herbs with stems prostrate, simple or branched; leaves opposite, petiolate, silvery-glaucous, orbicular to ovate, fleshy, glabrous; inflorescences dense cymes; sepals 5, ovate, not keeled, with hyaline margins, rounded at apex; petals 5, oblong, obtuse at apex; stamens 3; seeds with smooth surface. This morphology resembles P. tetraphyllum subsp. alsinifolium (Biv.) Ball and P. tetraphyllum subsp. diphyllum (Cav.) O. Bolòs & Font Quer (both occurring in Menorca), and several characters overlap. The taxon dunense can be distinguished on the basis of the height of the plants [up to 1 cm, with branches up to 3 cm vs 5-15(-20) cm (subsp. alsinifolium) or (3-)6-8(-10) cm (subsp. diphyllum)], the colour of the leaves [silvery-glaucous vs green to reddish or purplish (both other subspecies)], the sepals [obtuse and not keeled vs acute and keeled (subsp. diphyllum) or subacute and sligthly keeled (subsp. alsinifolium)], and the number of the stamens [3 vs 4 or 5 (both other subspecies)]. From the ecological point of view, the taxon dunense grows on mobile sand dunes, whereas subsp. alsinifolium and subsp. diphyllum occupy fixed sandy soils (see Fraga & Rosselló 2011).

    Considering the morphology, ecology and distribution of the taxon dunense and its obvious affinities with Polycarpon tetraphyllum, subspecies rank is appropriate, notably in view of the overlap of characters mentioned above. D. Iamonico

  • Silene muscipula L.

    + Bl(I): [Ibiza]: in Ebuso, sa Plana de Santa Agnès, 30 May 1918, Gros (BC 109923). — The presence of this species in the W Balearic Islands has been regarded as questionable by several authors (Talavera 1990; Marhold 2011). The herbarium specimen indicated above confirms the presence of Silene muscipula in Ibiza. In the Balearic archipelago this species was previously known from Mallorca and Menorca.

    L. Sáez

Fig. 1.

Vincetoxicum mugodsharicum — Russia, Samara province, Pohvistnevo district, mountain Kopeika, 5 Jun 2014, photograph by A. V. Ivanova.

f01_119.jpg

Compositae

  • Hieracium murorum subsp. asterophorum (Zahn) Zahn

    Ga(F): The questionable record for France given in Med-Checklist (Greuter 2008: 383) is erroneous. The only place cited by Zahn (1906: 393; 1921: 320; 1930–1935: 458) is Mount Grammont, which is in Switzerland, c. 4.5 km from the French border.

    E. von Raab-Straube & J.-M. Tison

  • Senecio inaequidens DC.

    A Gr: Greece, W Makedonia: Nomos and Eparchia of Kastoria, SE of Fotini, 40°31′30″N, 21°23′20″E, 675 m, herbaceous vegetation between road and fruit plantation, 6 Oct 2014, Willing & Willing 249558 (B, herb. Willing). — First record for Greece of this highly invasive xenophyte of S African origin, which is now fully established in NW and C Europe and reached Bulgaria in 2009 (Vladimirov & Petrova 2009). In Greece a future spread of the species along railway tracks, roads and highways and in urban habitats is expected and should be attentively monitored by local field botanists and nature conservationists. E. Willing & Th. Raus

Cruciferae

  • Cardamine hamiltonii G. Don (≡ Cardamine debilis D. Don, nom. illeg. ≡ C. flexuosa subsp. debilis O. E. Schulz).

    A Cr: Greece, Kriti (Crete): Nomos of Iraklion, Eparchia of Temenos, 1821 Street, near entrance of the “El Greco Hotel”, 35°20′16.9″N, 25°7′57.5″E, 30 m, edge of flower bed with a cultivated tree, 17 Jun 2014, Ardenghi & Cauzzi (MSNM). — The plant was probably introduced as a weed from plant nurseries, as in the other European localities where this spreading SE Asian alien has been recently recorded (see Ardenghi & Mossini 2014). Following Lihová & al. (2006) and Al-Shehbaz & al. (2010: 474), we recognize this taxon at specific rank, adopting the available binomial Cardamine hamiltonii.

    N. M. G. Ardenghi,

    P. Cauzzi & G. Galasso

Fig. 2.

Euphorbia hypericifolia — seeds. — Photograph by K. Sutorý.

f02_119.jpg

Euphorbiaceae

  • Euphorbia hypericifolia L.

    (≡ Chamaesyce hypericifolia (L.) Millsp.). — Fig. 2 & 3.

    A Gr: Greece: Nomos of Achaia, Eparchia of Egialia, on the N coastline of the Peloponnese peninsula, village Eleonos (W of Diakopto), 28°11′50″N. 22°10′40″E, near sea-level, in the street, 7 Aug 2013, Sutorý (BRNM). — The annual, more or less erect plants of Euphorbia subg. Chamaesyce Raf., originating from the neotropics, are sometimes separated as E. subsect. Hypericifoliae Boiss. Though modern methods do not accept this subsection in its original sense (Yang & Berry 2011), they are morphologically quite well distinguished from the other members of the subgenus. From this subsection at least two species are recognized as naturalized in Europe. Euphorbia nutans Lag. (≡ Chamaesyce nutans (Lag.) Small) is by far the commoner of the two. It is an expansive and often quite abundant xenophyte in the W part of the Mediterranean area (e.g. Greuter & al. 1986; Benedí 2000; Conti & al. 2005; Celesti-Grapow & al. 2009). It is less common in the E Mediterranean although it has been repeatedly recorded in recent times (e.g. Bergmeier 2007; Haber & Semaan 2007; Parolly & Eren 2007; Anastasiu & Negrean 2008; Biel & Tan 2009; Pahlevani & Riina 2011). The second species, E. hypericifolia (≡ C. hypericifolia), is distinguished from E. nutans by “fruits 0.9–1.3 mm long; columella < 1 mm long; transverse ribs on seeds often poorly defined, giving a pitted or irregular surface [Fig. 2]; inflorescences usually with leafless distal nodes; stipules usually 1–1.5 mm long and conspicuous [Fig. 3]” against “fruits 1.4–2 mm long; columella more than 1 mm long; transverse ribs on the seeds usually prominent and well defined; inflorescences with narrow reduced leaves at distal nodes; stipules usually c. 0.5 mm long and inconspicuous” (Burger & Huft 1995: 73). It was reported by Greuter & al. (1986) from Egypt, Israel and Italy, but the latter record (from Lombardia) is erroneous and referable to E. nutans (Banfi & Galasso 2010). Verloove (2002, 2005) cited two localities in Belgium (ephemeral) and Spain (degree of naturalization uncertain). Recently, it was also reported from Crete (Gregor & Meierott 2013). Plants of E. hypericifolia were found in 2013 on the N coastline of Peloponnisos in Greece, in the streets of Eleonos (W of Diakopto). A targeted search in the same locality as well as in neighbouring villages in 2014 was not successful. We can assume that its occurrence there is not common.

    Considering the distribution in Europe and Macaronesia, Euphorbia hypericifolia is doubtless most widespread in the Canary Islands (El Hierro, La Palma, La Gomera, Tenerife, Gran Canaria and Fuerteventura; see Acebes & al. 2009; Santos-Guerra & al. 2013; Otto & Verloove 2014), from which area it is surprisingly omitted in the Euro+Med PlantBase (Euro+Med 2006+).

    Euphorbia hypericifolia is a fairly variable species. Present-day taxonomists mostly tend to accept it in a broad sense (see, e.g.,  http://www.tropicos.org/. However, if a narrow species concept would apply, then all plants seen from Europe (with quite glabrous stems and leaves) should be assigned to E. glomerifera (Millsp.) L. C. Wheeler (≡ Chamaesyce glomerifera Millsp.). Carter & al. (1984) came to the same conclusion with respect to plants from the Cape Verde Islands. K. Sutorý & P. Verloove

Fig. 3.

Euphorbia hypericifolia — stipules. — Photograph by K. Sutorý.

f03_119.jpg

Guttiferae

  • Hypericum dubium Leers [= Hypericum maculatum subsp. obtusiusculum (Tourlet) Hayek].

    + Ct: Croatia: Međimurska županija, 0.5 km W of Zasadbreg, 46°27′N, 16°23′24″E, 250 m, on the margin of a hay meadow, 1 Jul 2013, Király (ZA). — First record for Croatia. Hypericum dubium, a representative of the H. maculatum Crantz group, is considered a separate species (Marhold 2011+; for nomenclature and taxonomy see Mártonfi 2008). It grows SE-E of the main range of the Alps on hay meadows in the submontane belt where it replaces H. maculatum s.str. (with which it was often confused in the region).

    G. Király

Malvaceae

  • Malva stenopetala subsp . plazzae (Atzei) Iamonico, Bartolucci & Peruzzi, comb. nov.Lavatera plazzae Atzei in Boll. Soc. Sarda Sci. Nat. 30: 151. 1995 ≡ Malva plazzae (Atzei) Soldano, Banfi & Galasso in Atti Soc. Ital. Sci. Nat. Mus. Civico Storia Nat. Milano 146: 230. 2005 ≡ Lavatera stenopetala subsp. plazzae (Atzei) Iamonico in Pl. Ecol. Evol. 147: 196. 2014. — Holotype: Italy, Sassari, fra la staz. ferrov. di Giave (c. 1 km) e la Cant, di Cadrea, ai bordi della vecchia SS Carlo Felice, 19 Jul 1991, Atzei B229bis (SASSA).

    A recent taxonomic and nomenclatural investigation on Lavatera stenopetala Batt. and L. plazzae Atzei clearly showed that these two taxa are distinct from morphological and chorological points of view, supporting a separation of the latter at subspecific rank (Iamonico 2014). The first author preliminarily accepted the recognition of these taxa under Lavatera L., given that several scholars (e.g. Bayer & Kubitzki 2003; Molero & Montserrat 2007) still accepted the genus Lavatera as distinct from Malva L., albeit limited to the taxa included in the so-called “lavateroid clade” as defined by Ray (1995).

    However, on the basis of the molecular studies by Ray (1995) himself, Tate & al. (2005) and Escobar & al. (2009), the traditional separation of Malva and Lavatera is certainly artificial and cannot be maintained. As a consequence, several names in Lavatera were transferred to Malva (see e.g. Banfi & al. 2005; Molero & Montserrat 2006; Iamonico 2010b; Conti & Bartolucci 2012), and this is the classification currently adopted also in Euro+Med PlantBase (Valdés 2011). In the checklist of Italian endemics (Peruzzi & al. 2014) and in the ongoing new edition of the Checklist of the Italian vascular flora (F. Conti and collaborators, in prep.), Malva is applied in its broadest sense. Hence, we here propose a new combination, necessary for accommodating L. plazzae at sub specific rank under Malva stenopetala (Batt.) Soldano & al.

    D. Iamonico, F. Bartolucci & L. Peruzzi

Onagraceae

  • Oenothera speciosa Nutt.

    A Cr: Greece, Kriti (Crete): Nomos & Eparchia of Chania, Episkopi, N and S sides of Eparchiaki Odos Chanion-Sougias, near the service station, 35°28′7.8″N, 23°55′32.2″E, 55 m, roadsides, 15 Jun 2014, Ardenghi & Cauzzi (MSNM; det. Ardenghi 2014). — Spontaneous individuals occurred on both sides of a road, originating from the dissemination of cultivated plants in the nearby service station.

    N. M. G. Ardenghi & P. Cauzzi

Orobanchaceae

  • Orobanche rapum-genistae Thuill.

    Bl: This species was recorded from Menorca by Marès & Vigineix (1880). According to Fraga & al. (2004) its presence in the Balearic Islands is questionable. Indeed, the voucher specimen that had served as base for this record “[Menorca] Fort St. Philippe, 21 May 1855, G. Vigineix (MPU-Knoche, sub Orobanche rapum)” belongs to O. crinita Viv. L. Sáez

Portulacaceae

  • Portulaca cypria Danin

    + Lu: Portugal: Soure [near Coimbra], Jul 1890, Moller (COI). — This is the first record of the microspecies from the Iberian peninsula.

    A. Danin & F. Sales

  • Portulaca granulatostellulata (Poelln.) Ricceri & Arrigoni

    + Ab(A): Azerbaijan: Gfi01_119.gifdfi01_119.gifbfi01_119.gify rayon, Qizilturpaq, near Zajamçay bridge on road to Qovlar, 40°36′16″N, 45°38′41″E, 1140 m, 29 Aug 2011, Raab-Straube 4660, Farzaliev & K∂rimov (B, BAK); Gfi01_119.gifncfi01_119.gif Şfi01_119.gifhfi01_119.gifri, Gfi01_119.gifncfi01_119.gif, near city centre, 40°40′N, 46°21′E, 450 m, garden, ruderal place, 30 Aug 2011, Raab-Straube 4688, Farzaliev & K∂rimov (B, BAK). — These are the first records of any microspecies of the Portulaca oleracea L. aggregate from Azerbaijan. From the Caucasus region, only P. granulatostellulata (Danin 2011a) and P. nitida (Danin & H. G. Baker) Ricceri & Arrigoni (Danin 2011b), both from Tbilisi (Georgia), have been reported so far.

    A. Danin & E. von Raab-Straube

Rosaceae

  • Pyrus austriaca A. Kern,

    C Ct: Croatia: Varaždinska županija, S of Bedenec, 46°14′14″N, 16°04′00″E, 230 m, a single tree in an orchard, 7 Sep 2013, Király & Schmidt (ZA); ibid.: near Gornja Voća, Király & Schmidt obs.; ibid.: Međimurska županija, Štrigova, Király & Schmidt obs. — First records for Croatia. Pyrus austriaca is often considered conspecific with P. nivalis. However, as a stable hybrid of P. nivalis Jacq. and P. pyraster (L.) Baumg. (see Terpó 1960) it is presumably a separate entity (Kurtto & al. 2013). Supposedly it is a primeval cultivated fruit tree, since it grows mostly in orchards and vineyards. Its range is limited to the E foot of the Alps. Certain former records of P. nivalis from SE Austria and N Slovenia also refer to P. austriaca (Király 2000; Király & al. 2007; for the status of the taxon in Austria see also Fischer & al. 2008: 539). Pyrus austriaca is a tree up to 15 m high (P. nivalis is usually not taller than 5 m), it never develops root suckers (P. nivalis forms large polycormons), and its leaves are generally at least 4–5 cm long with yellowish felt on the lower surface (leaves of P. nivalis are rarely longer than 4 cm, with white felt). Pyrus austriaca differs from P. nivalis also by its glabrous style. G. Király

  • Rubus armeniacus Focke

    N BH: Bosnia and Herzegovina: Canton of Una-Sana, Donji Vojići, 1.5 km SW of the village along the road nr M-5, 44°32′55″N, 16°41′48″E, 475 m, shrubbery, 29 Sep 2013, Király & al. (BP). — First verified record of this Caucasian apomictic bramble species of Rubus [sect. Rubus] ser. Discolores (P. J. Müll.) Focke for Bosnia and Herzegovina and the Balkan peninsula as a whole (for the European distribution see Kurtto & al. 2010). The species is highly invasive in some parts of C Europe and North America (Weber 1995), hence a further expansion in SE Europe is also to be expected. G. Király, Z. Barina & D. Pifkó

  • Rubus bifrons Vest

    + BH: Bosnia and Herzegovina: Canton of Una-Sana, 1.3 km E of Zgon along the road to Sanski Most, 44°33′11″N, 16°48′37″E, 360 m, shrubbery, 29 Sep 2013, Király & al. (BP); ibid.: 8.5 km N of Zgon along the road to Sanski Most, 44°37′59″N, 16°47′56″E, 215 m, shrubbery, 29 Sep 2013, Király & al. obs.; ibid.: 3.5 km E of Donji Vojići, parking place along the road nr M-5, 44°33′05″N, 16°40′01″E, 635 m, 29 Sep 2013, Király & al. obs. — A bramble species of a wide sub-Mediterranean to C European distribution, reported in the N Balkan Peninsula from Croatia and Slovenia; however, its presence in Bosnia and Herzegovina was questioned by Kurtto & al. (2010). Based on our observations, it can be considered a widespread species of mesic forest fringes in the NW part of the country. G. Király, Z. Barina & D. Pifkó

Commelinaceae

  • Commelina erecta L.

    A Ir: Israel: Jerusalem, Bet Hakerem, 14 Sep 2014, Danin (B, HUJ, PAL); ibid.: Lower Galilee, Yifaat, 15 Sep 2014, Danin (HUJ). — A weed native to North America and Africa that has not yet been recorded from the E Mediterranean area. It seems to have been recently introduced in Israel. A. Danin

Gramineae

  • Melinis repens (Willd.) Zizka subsp. repens

    A It: Italy, Campania: Province of Salerno, Salerno, via Ligea, 40°40′27.3″N, 14°44′14.3″E, near sealevel, roadsides, 29 Sep 2002, Del Guacchio & Petolicchio (NAP, herb. Del Guacchio). — Melinis repens is native to Africa and S W Asia, but nowadays it is reported as an alien species also in the Americas, Europe and Oceania (Verloove & Sánchez Gullón 2008). The single individual found fits well within the most widespread subspecies M. repens subsp. repens (Clayton 1989: 117). Valdés & Scholz (2009) reported it in the Euro-Mediterranean area only for the Canary Islands. However, the record of the species for Spain (cf. Valdés & Scholz 2009) is also to be referred to the same taxon (Verloove & Sánchez Gullón 2008). No previous records are given in Italian standard floras (see, e.g., Conti & al. 2005, 2007; Celesti-Grapow & al. 2010 and literature therein). At present, the species is obviously to be regarded as a casual alien in Italy where the genus itself is new. Even if M. repens is also used as an ornamental plant (Knees & Zantout 2011), it is not cultivated in the area of our find, where several other species have probably been introduced casually by maritime trade. Among them we may mention the very rare Acalypha ostryifolia J. M. Coult. (Euphorbiaceae) (Del Guacchio 2005), not recorded by Euro+Med PlantBase (Euro+Med 2006+). E. Del Guacchio

  • Sporobolus cryptandrus (Torr.) A. Gray

    N It: Italy, Toscana: Tenuta di San Rossore (Pisa), Viale delle Cascine, Regional Park of Migliarino San Rossore Massaciuccoli, 43°43′04″N, 10°20′16″ E, near sea-level, xeric grassland rich in therophytes, 28 Aug 2014, Sani & D'Antraccoli (PI). — Sporobolus R. Br. is a cosmopolitan genus, belonging to subfamily Chloridoideae, tribe Zoysieae, subtribe Sporobolinae (Peterson & al. 2007). It is one of the largest genera within the subfamily, including about 200 species (Simon & al. 2011), predominantly distributed in the tropical and subtropical areas of the world, especially in Africa (73 spp.), North America (45 spp.), and Asia (34 spp.) (Ortiz-Diaz & Culham 2000). At present, four species of Sporobolus are recorded in Italy (Conti & al. 2005): S. indicus (L.) R. Br., S. neglectus Nash and S. vaginiflorus (Torr.) Wood are alien species (Celesti-Grapow & al. 2010), whereas S. virginicus Kunth is native. Sporobolus cryptandrus is native to North America, where it is widespread throughout S Canada, across most of the United States, and N Mexico (Hitchcock 1950). In Europe, it is recorded as alien for France (Tison & de Foucault 2014), Germany and Slovakia (Valdés & Scholz 2009) and Austria and Hungary (DAISIE 2008). This is the first record for the Italian flora. For the identification, the keys published by Hitchcock (1950) and Tison & de Foucault (2014) were used.

    A. Sani, M. D'Antraccoli & L. Peruzzi

Liliaceae

  • Lilium jankae A. Kern.

    + Gr: Greece, N Thessalia/W Makedonia: Nomos of Larisa/Pieria, Eparchia of Elasson/Pieria: Mt Titaros, between Livadion and Skotina, 40°11′N, 22°09′E, opening in Fagus forest on N-facing slope, 27 Jul 1976, Andersen 11248 (G). — This previously overlooked collection clearly represents Lilium jankae rather than the closely related L. albanicum Griseb. Rešetnik & al. (2007) recognized four geographically vicariant members of the L. carniolicum group: L. carniolicum W. D. J. Koch in the SE Alps; L. bosniacum (Beck) Fritsch from Istria to Montenegro; L. albanicum from Montenegro to NW Greece; and L. jankae from Bulgaria, E Serbia and SW Romania. In fact, L. albanicum and L. jankae meet in the mountains of NC and NE Greece. Whereas Andersen 11248 clearly represents L. jankae, other collections are more or less intermediate, notably some from Mt Belles (Kerkini) on the Greek/Bulgarian border, viz. Strid & al. 16181 (G, herb. A. Strid) and Strid & al. 18555 (B, C) = Stamatiadou 22509 (ATH). Collections from Mt Pieria and Mt Vermio are also more or less intermediate, whereas plants from Mt Siniatsiko, Mt Vitsi and further W are rather typical L. albanicum. In view of the somewhat vague morphological differences and vicariant distribution areas, the four members of the L. carniolicum group may be better regarded as geographical races (subspecies). A. Strid

  • Tulipa rhodopea (Velen.) Velen.

    + Gr: Greece, E Makedonia: Nomos & Eparchia of Xanthi: Near Xanthi, Meken Tepe, 41°11′N, 24°48′E, c. 700 m, rock ledges on very steep slope of limestone hills, 1 May 1936, Tedd 1665 (K 3 sheets; images available online at  http://apps.kew.org/herbcat/navigator.do). [The locality has not been precisely identified, but probably refers to hills a few km NNW of Xanthi]. — This large, red-flowered tulip was first described as Tulipa orientalis var. rhodopea Velen. (Velenovský 1900: 8, “in lapidosis m. Rhodope ad Sv. Petka” [Bulgaria]). It was subsequently recombined as T. rhodopea by Velenovský in Reliquiae Mrkvičkanae (Velenovský 1922: 28), a little-known publication listing plants collected by Jan Mrkvička, who was a soldier with the Bulgarian army in Macedonia in 1915–1916 and who collected plants during that campaign. Mrkvička had collected this tulip on Pirin Planina in SW Bulgaria near the Greek border. After he was killed in action on 17 Aug 1916, his specimens were sent to his parents, who handed them over to Velenovský. H. Griffith Tedd was a British amateur botanist who lived in Xanthi for several years in the 1930s, associated with the tobacco industry that flourished in NE Greece at that time. He gathered some 2000 generally well-prepared and well-labelled specimens, which were sent to William B. Turrill at Kew for identification. Tedd used the old Turkish geographical names, which are not always easy to identify with their modern Greek equivalents. Tulipa rhodopea was previously believed to be endemic to a small area in SW Bulgaria. Its taxonomic status is somewhat uncertain. In the recent monograph of Tulipa L. (Everett 2013: 236–237), it was listed as a synonym of T. hungarica Borbás, and was said to be “naturalizing well in a border at Kew”.

    A. Strid

Palmea

  • Washingtonian filiera (Andre) de Barry

    A Car: Greece, Kriti (Crete): Nomos & Eparchia of Chania, Episkopi, N side of the Eparchiaki Odos Chanion-Sougias, 35°28′5.3″N. 23°55′27.8″E, 55 m, dry ditch along the road, 15 Jun 2014, Ardenghi & Cauzzi (MSNM; det. Ardenghi 2014). — The observed juvenile individuals (at least one year old) originated from the dissemination of plants possibly cultivated in nearby private gardens.

    N. M. G. Ardenghi & P. Cauzzi

Corrigendum to Euro+Med-Checklist Notulae, 3

Pilosella acutifolia subsp. villarsii (F. W. Schultz & Sch. Bip.) Gottschl, in Willdenowia 44: 291. 2014 ≡ Pilosella villarsii F. W. Schultz & Sch. Bip. in Flora 45: 242. 1862 ≡ Hieracium villarsii F. W. Schultz in Flora 44: 35. 1861 [non J. Serres in Bull. Soc. Bot. France 2: 225. 1855] ≡ Hieracium brachiatum subsp. villarsii (F. W. Schultz & Sch. Bip.) Nägeli & Peter, Hierac. Mitt.-Eur. 1: 616. 1885 ≡ Pilosella brachiata subsp. villarsii (F. W. Schultz & Sch. Bip.) Schuhw. in Ber. Bayer. Bot. Ges. 83: 199. 2013.

Gottschlich, when providing the new combination in Pilosella acutifolia, overlooked that Hieracium villarsii F. W. Schultz is illegitimate, being a later homonym, and P. villarsii therefore is to be treated as a replacement name with the same type (McNeill & al. 2012: Art. 58.1). Later combinations have to be based on this replacement name. The new combination was validly published because Gottschlich also cited the actual basionym with a full and direct reference to its author and place of valid publication (Art. 41.5); also, contrary to what was stated, the combination P. brachiata subsp. villarsii was validly published by Schuhwerk in 2013.

References

  1. J. R. Acebes , M. C. León , M. L. Rodríguez , M. del Arco , A. García , P. L. Pérez , O. Rodríguez , V. E. Martín & W. Wildpret de la Torre 2009: Pteridophyta, Spermatophyta. — Pp. 119–172 in: M. Arechavaleta , S. Rodríguez , N. Zurita & A. García (ed.), Lista de especies silvestres de Canarias (hongos, plantas y animales terrestres), ed. 2. — La Laguna: Gobierno de Canarias. Google Scholar

  2. I. A. Al-Shehbaz , K. Marhold & J. Lihová 2010: Cardamine. — Pp. 464–484 in: Flora of North America Editorial Committee (ed.), Flora of North America North of Mexico 7. — New York & Oxford: Oxford University Press. Google Scholar

  3. P. Anastasiu & G. Negrean 2008: Plante străine noi în România. New alien plants to Romania. — Analele Univ. Craiova, Agric. Montan. Cadastra 38/B: 1–10. Google Scholar

  4. N. M. G. Ardenghi & S. Mossini 2014: Cardamine flexuosa subsp. debilis O. E. Schulz. — P. 292 in: E. von Raab-Straube & Th. Raus (ed.): Euro+Med-Checklist Notulae, 3 [Notulae ad floram euro-mediterraneam pertinentes 32]. —  Willdenowia 44: 287–299 Google Scholar

  5. E. Banfi & G. Galasso (ed.) 2010: La flora esotica lombarda. — Milano: Museo di Storia Naturale di Milano. Google Scholar

  6. E. Banfi , G. Galasso & A. Soldano 2005: Notes on systematics and taxonomy for the Italian vascular flora 1. — Atti Soc. Ital. Sci. Nat. Mus. Civico Storia Nat. Milano 146: 219–244. Google Scholar

  7. C. Bayer & K. Kubitzki 2003: Malvaceae. — Pp. 225–311 in: K. Kubitzki & C. Bayer (ed.), Families and genera of vascular plants 5. — Berlin & New York: Springer. Google Scholar

  8. C. Benedí 2000: Chamaesyce Gray. — Pp. 286–297 in: S. Castroviejo , C. Aedo , C. Benedí , M. Laínz , F. Muñoz Garmendia , G. Nieto Feliner & J. Paiva (ed.), Flora iberica. Plantas vasculares de la Península Ibérica e Islas Baleares 8. Haloragaceae-Euphorbiaceae. — Madrid: Real Jardín Botánico, CSIC. Google Scholar

  9. E. Bergmeier 2007: Chamaesyce nutans. — P. 439 in: W. Greuter & Th. Raus (ed.), Med-Checklist Notulae, 26. —  Willdenowia 37: 435–444 Google Scholar

  10. B. Biel & K. Tan 2009: Contribution 22 Chamaesyce nutans. — P. 435 in: V. Vladimirov , F. Dane , V. Stevanović & K. Tan : New floristic records in the Balkans: 12. — Phytol. Balcan. 15: 431–452. Google Scholar

  11. O. Bolòs & J. Vigo 1996: Flora dels Països Catalans 3. — Barcelona: Barcino. Google Scholar

  12. W. Burger & M. Huft 1995: Flora costaricensis. Family 113 Euphorbiaceae. — Fieldiana, ser. 2, 36. Google Scholar

  13. J. Cambessèdes 1827: Enumeratio plantarum quas in insulis Balearibus collegit J. Cambessèdes. —  Mém. Mus. Hist. Nat. Paris 14: 173–335 Google Scholar

  14. S. Carter , W. Lobin & A. Radcliffe-Smith 1984: A collection of and notes on Euphorbiaceae from the Cape Verde Islands (Dicotyledonae). — Senckenberg. Biol. 64: 429–451. Google Scholar

  15. L. Celesti-Grapow , L. Pretto , G. Brundu , E. Carli & C. Blasi 2009: A thematic contribution to the National Biodiversity strategy. Plant invasion in Italy, an overview. — Roma: Palombi. Google Scholar

  16. L. Celesti-Grapow , F. Pretto , E. Carli & C. Blasi (ed.) 2010: Flora vascolare alloctona e invasiva delle regioni d'Italia. — Roma: Università La Sapienza. Google Scholar

  17. W. D. Clayton 1989: Melinis Beauv. — Pp. 115–128 in: E. Launert & G. Pope (ed.), Flora zambesiaca 10(3). — London: Flora Zambesiaca Managing Committee. — Published at:  http://apps.kew.org/efloras/search.do [accessed 7 Jun 2013]. Google Scholar

  18. F. Conti , G. Abbate , A. Alessandrini & C. Blasi (ed.) 2005: An annotated checklist of the Italian vascular flora. — Roma: Palombi. Google Scholar

  19. F. Conti , A. Alessandrini , G. Bacchetta , E. Banfi , G. Barberis , F. Bartolucci , L. Bernardo , S. Bonacquisti , D. Bouvet , M. Bovio , G. Brusa , E. Del Guacchio , B. Foggi , S. Frattini , G. Galasso , L. Gallo , C. Gangale , G. Gottschlich , P. Grünanger , L. Gubellini , G. Iiriti , D. Lucarini , D. Marchetti , B. Moraldo , L. Peruzzi , L. Poldini , F. Prosser , M. Raffaelli , A. Santangelo , E. Scassellati , S. Scortegagna , F. Selvi , A. Soldano , D. Tinti , D. Ubaldi , D. Uzunov & M. Vidali 2007: Integrazioni alla Checklist della flora vascolare italiana. — Nat. Vicentina 10: 5–74. Google Scholar

  20. F. Conti & F. Bartolucci 2012: Two new combinations in Malva (Malvaceae). — Ann. Bot. Fenn. 49: 123–124. Google Scholar

  21. DAISIE 2008: European Invasive Alien Species Gateway. — Published at  http://www.europe-aliens.org/ [accessed 26 Nov 2014]. Google Scholar

  22. A. Danin 2011a: Portulacaceae. — Pp. 131–134 in: W. Greuter & E. von Raab-Straube (ed.), Euro+Med Notulae, 5. —  Willdenowia 41: 129–138 Google Scholar

  23. A. Danin 2011b: Collections of microspecies of the Portulaca oleracea aggregate from Europe and the Mediterranean areas. — Fl. Medit. 21: 305–307. Google Scholar

  24. E. Del Guacchio 2005: New data for the exotic flora of Campania. — Quad. Bot. Amb. Appl. 16: 175–180. Google Scholar

  25. P. Escobar , P. Schönswetter , J. Fuertes Aguilar , G. Nieto Feliner & G. M. Schneeweiss 2009: Five molecular markers reveal extensive morphological homoplasy and reticulate evolution in the Malva alliance (Malvaceae). —  Molec. Phylogen. Evol. 50: 226–239. Google Scholar

  26. Euro+Med 2006+ [continuously updated]: Euro+Med PlantBase — the information resource for Euro-Mediterranean plant diversity. — Published at  http://ww2.bgbm.org/EuroPlusMed [accessed 19 Dec 2014]. Google Scholar

  27. D. Everett 2013: The genus Tulipa. Tulips of the world. — Kew: Royal Botanic Gardens. Google Scholar

  28. M. Fischer , K. Oswald & W. Adler 2008: Exkursionsflora für Österreich, Liechtenstein und Südtirol, ed. 3. — Linz: Biologiezentrum der Oberösterreichischen Landesmuseen. Google Scholar

  29. P. Fraga , C. Mascaró , D. Carreras , O. Garcia , X. Pellicer , M. Pons , M. Seoane & M. Truyol 2004: Catàleg de la flora vascular de Menorca. — Maó: Institut Menorqui d'Estudis IME. Google Scholar

  30. P. Fraga & J. A. Rosselló 2011: Polycarpon dunense (Caryophyllaceae), a new psammophilous species from Minorca (Balearic islands). — Flora Montiber. 47: 29–35. Google Scholar

  31. T. Gregor & L. Meierott 2013: Report 72 Euphorbia hypericifolia L. — P. 277 in: V. Vladimirov , F. Dane , V. Stevanovič & K. Tan , New floristic records in the Balkans: 22. — Phytol. Balcan. 19: 267–303. Google Scholar

  32. W. Greuter 2008: Dicotyledones (Compositae). — In: W. Greuter & E. von Raab-Straube (ed.), Med-Checklist 2. — Palermo, Genève & Berlin: OPTIMA. Google Scholar

  33. W. Greuter , H. M. Burdet & D. Long (ed.) 1986: Med-Checklist 3. — Genève: Conservatoire et Jardin botaniques de la Ville de Genève; Berlin: Secretariat Med-Checklist, Botanischer Garten & Botanisches Museum Berlin-Dahlem. Google Scholar

  34. W. Greuter & E. von Raab-Straube (ed.) 2005: Euro+Med Notulae, 1. —  Willdenowia 35: 223–239. Google Scholar

  35. R. M. Haber & M. T. Semaan 2007: Two records from Lebanon: Camaesyce nutans (Lag.) Small (Euphorbiaceae) and Eleusine indica (L.) Gaertner (Poaceae). — Turk. J. Bot. 31: 341–343. Google Scholar

  36. A. S. Hitchcock 1950: Manual of the grasses of the United States. Miscellaneous publication no. 200, revised by Agnes Chase. — Washington, DC: United States Goverment Printing Office. Google Scholar

  37. D. Iamonico 2010a: Amaranthus tamariscinus Nutt. (Amaranthaceae): taxonomical notes on the species and its presence in Italy. — Nat. Sloveniae 12: 25–33. Google Scholar

  38. D. Iamonico 2010b: Malva subovata subsp. bicolor, comb. & stat, nov. (Malvaceae). —  Ann. Bot. Fenn. 47: 312–314. Google Scholar

  39. D. Iamonico 2013: Notula 1997. Polycarpon tetraphyllum L. subsp. polycarpoides (Biv.) Iamonico stat. nov. (Caryophyllaceae). Notulae nomenclaturali alla Checklist della flora italiana: 15. — Inform. Bot. Ital. 45: 105. Google Scholar

  40. D. Iamonico 2014: Lavatera stenopetala subsp. plazzae comb, et stat. nov. —  Pl. Ecol. Evol. 147: 293–298 Google Scholar

  41. D. Iamonico 2015: A new nomenclatural change in Polycarpon (Caryophyllaceae): P. tetraphyllum subsp. sauvagei comb. & stat, nov., an endemic taxon from Morocco. —  Phytotaxa 197: 225–26. Google Scholar

  42. D. Iamonico & G. Domina 2015: Nomenclatural notes on the Polycarpon tetraphyllum aggregate (Caryophyllaceae). — Pl. Biosystems (in press). Google Scholar

  43. G. Király 2000: Neue Ergebnisse der floristischen Forschung im westlichen Grenzgebiet Ungarns. — Verh. Zool.-Bot. Ges. Österreich 137: 235–254. Google Scholar

  44. G. Király , A. Mesterházy & B. Bakan 2007: Elodea nuttalii (Planch.) H. St. John, Myosotis laxa Lehm, and Pyrus austriaca Kern., new for Slovenia, as well as other floristic records. — Hladnikia 20: 11–15. Google Scholar

  45. S. G. Knees & N. Zantout 2011: Melinis. — P. 357 in: J. Cullen , S. G. Knees & H. S. Cubey (ed.), The European garden flora 1. — Cambridge: University Press. Google Scholar

  46. A. Kool , A. Bengtson & M. Thulin 2007: Polyphyly of Polycarpon (Caryophyllaceae) inferred from DNA sequence data. —  Taxon 56: 775–782. Google Scholar

  47. A. Kurtto , A. N. Sennikov & R. Lampinen (ed.) 2013: Atlas florae europaeae 16. Rosaceae (Cydonia to Prunus, excl. Sorbus). — Helsinki: Committee for Mapping the Flora of Europe & Societas Biologica Fennica Vanamo. Google Scholar

  48. A. Kurtto , H. E. Weber , R. Lampinen & A. N. Sennikov (ed.) 2010: Atlas florae europaeae 15. Rosaceae (Rubus). — Helsinki: Committee for Mapping the Flora of Europe & Societas Biologica Fennica Vanamo. Google Scholar

  49. J. Lihová , K. Marhold , H. Kudoh & M. A. Koch 2006: Worldwide phylogeny and biogeography of Cardamine flexuosa (Brassicaceae) and its relatives. —  Amer. J. Bot. 93: 1206–1221 Google Scholar

  50. P. Marès & G. Vigineix 1880: Catalogue raisonné des plantes vasculaires des îles Baléares. — Paris: G. Masson. Google Scholar

  51. K. Marhold 2011+ [continuously updated]: Caryophyllaceae, Clusiaceae. — In: Euro+Med PlantBase — the information resource for Euro-Mediterranean plant diversity. — Published at  http://ww2.bgbm.org/EuroPlusMed [accessed 7 Dec 2014]. Google Scholar

  52. P. Mártonfi 2008: Hypericum dubium Leers — new data on taxonomy and biology. —  Folia Geobot. 43: 59–82. Google Scholar

  53. J. McNeill , F. R. Barrie , W. R. Buck , V. Demoulin , W. Greuter , D. L. Hawksworth , P. S. Herendeen , S. Knapp , K. Marhold , J. Prado , W. F. Prud'homme van Reine , G. F. Smith , J. H. Wiersema & N. J. Turland (ed.) 2012: International Code of Nomenclature for algae, fungi, and plants (Melbourne Code) adopted by the Eighteenth International Botanical Congress Melbourne, Australia, July 2011. — Regnum Veg. 154. Google Scholar

  54. J. Molero & J. M. Montserrat 2006: Adiciones y enmiendas nomenclaturales en el género Malva L. (Malvaceae). — Lagascalia 26: 153–155. Google Scholar

  55. J. Molero & J. M. Montserrat 2007: A new species of Lavatera sect. Olbia (Medik.) DC. (Malvaceae) from north-east Morocco. —  Bot. J. Linn. Soc. 153: 445–454. Google Scholar

  56. S. L. Mosyakin & K. R. Robertson 1996: New infrageneric taxa and combinations in Amaranthus (Amaranthaceae). — Ann. Bot. Fenn. 33: 275–281. Google Scholar

  57. S. L. Mosyakin & K. R. Robertson 2003: Amaranthus L. — Pp. 410–435 in: Flora of North America Editorial Committee (ed.), Flora of North America North of Mexico 4. — New York & Oxford: Oxford University Press. Google Scholar

  58. NOBANIS 2013: European Network on Invasive Alien Species. — Published at  http://www.nobanis.org/ [accessed 15 Jan 2015]. Google Scholar

  59. J. J. Ortiz-Diaz & A. Culham 2000: Phylogenetic relationships of the genus Sporobolus (Poaceae: Eragrostideae) based on nuclear ribosomal DNA ITS sequences. — Pp. 184–188 in: S. W. L. Jacobs & J. Everett (ed.), Grasses: systematics and evolution. — Collingwood: CSIRO Publishing. Google Scholar

  60. R. Otto & F. Verloove 2015: New xenophytes from La Palma (Canary Islands, Spain), with emphasis on naturalized and (potentially) invasive species. — Collect. Bot. (Barcelona) (in press). Google Scholar

  61. A. H. Pahlevani & R. Riina 2011: A synopsis of Euphorbia subgen. Chamaesyce (Euphorbiaceae) in Iran. —  Ann. Bot. Fenn. 48: 304–316. Google Scholar

  62. G. Parolly & Ö. Eren 2007: Contributions to the flora of Turkey. —  Willdenowia 37: 243–271. Google Scholar

  63. L. Peruzzi , F. Conti & F. Bartolucci 2014: An inventory of vascular plants endemic to Italy. —  Phytotaxa 168: 1–75 Google Scholar

  64. P. M. Peterson , J. T. Columbus & S. J. Pennington 2007: Classification and biogeography of New World grasses: Chloridoideae. —  Aliso 23: 580–594. Google Scholar

  65. E. G. Pobedimova 1952: Asclepiadaceae Lindl. — Pp. 663–718 in: B. K. Shishkin & E. G. Bobrov (ed.), Flora URSS 18. — Moskva & Leningrad: Akademii Nauk SSSR. Google Scholar

  66. E. von Raab-Straube & Th. Raus (ed.) 2014: Euro+Med-Checklist Notulae, 3 [Notulae ad floram euro-mediterraneam pertinentes 31]. —  Willdenowia 44: 287–299 Google Scholar

  67. M. F. Ray 1995: Systematics of Lavatera and Malva (Malvaceae, Malveae): a new perspective. —  Pl. Syst. Evol. 198: 29–53 Google Scholar

  68. L Rešetnik , Z. Liber , Z. Satovic , P. Cigić & T. Nikolić 2007: Molecular phylogeny and systematics of the Lilium carniolicum group (Liliaceae) based on nuclear ITS sequences. —  Pl. Syst. Evol. 265: 45–58 Google Scholar

  69. Z. N. Rjabinina & M. S. Knjazev 2009: Opredelitel' sosudistyh rastenij Orenburgskoj oblasti. — Moskva: Tovariščestvo naučnyh izdanij KMK. Google Scholar

  70. A. Santos-Guerra , J. A. Reyes-Betancort , M. A. Padrón-Mederos & R. Mesa-Coello 2013: Plantas poco o nada conocidas de la flora vascular silvestre de las Islas Canarias. — Bot. Complut. 37: 99–108. Google Scholar

  71. B. K. Simon , W. D. Clayton , K. T. Harman , D. Healy & Y. Alfonso 2011: GrassWorld. — Published at  http://grassworld.myspecies.info/ [accessed 10 Nov 2014]. Google Scholar

  72. S. Talavera 1990: Silene L. — Pp. 313–406 in: S. Castroviejo , M. Lainz , G. López González , P. Montserrat , F. Muñoz Garmendia , J. Paiva & L. Villar (ed.), Flora iberica. Plantas vasculares de la Península Ibérica e Islas Baleares 2. Platanaceae-Plumbaginaceae (partim). — Madrid: Real Jardín Botánico, CSIC. Google Scholar

  73. J. A. Tate , J. Fuertes Aguilar , S. J. Wagstaff , J. C. La Duke , T. A. B. Slotta & B. B. Simpson 2005: Phylogenetic relationships within the tribe Malveae (Malvaceae, subfamily Malvoideae) as inferred from ITS sequence data. —  Amer. J. Bot. 92: 584–602. Google Scholar

  74. A. Terpó 1960: Magyarország vadkörtéi (Pyri Hungariae). — Kert. Szőlész. Főisk. Évk. 11: 1–258. Google Scholar

  75. J.-M. Tison & B. de Foucault 2014: Flora gallica. Flore de France. — Mèze: Biotope. Google Scholar

  76. B. Valdés 2011: Malvaceae. — Pp. 318–319 in: W. Greuter & Th. Raus (ed.), Med-Checklist Notulae, 30. —  Willdenowia 41: 311–328. Google Scholar

  77. B. Valdés 2012: Myosotis L. — Pp. 490–527 in: S. Castroviejo (ed.), Flora iberica. Plantas vasculares de la Península Ibérica e Islas Baleares 11. Gentianaceae-Boraginaceae. — Madrid: Real Jardín Botánico, CSIC. Google Scholar

  78. B. Valdés & H. Scholz 2009: Poaceae (pro parte majore). — In: Euro+Med PlantBase — the information resource for Euro-Mediterranean plant diversity. — Published at  http://ww2.bgbm.org/euroPlusmed/ [accessed 8 Nov 2014, 19 Dec 2014]. Google Scholar

  79. V. M. Vasjukov , A. V. Ivanova & S. A. Senator 2014: On the flora of Great Basin Kinel (Samara region) — Pp. 43–47 in: S. A. Senator , S. V. Saksonov & G. S. Rozenberg (ed.), Ecology and geography of plants and communities of the middle Volga. — Togliatti: Cassandra. Google Scholar

  80. J. Velenovský 1900: Siebenter Nachtrag zur Flora von Bulgarien. — Sitzungsber. Königl. Böhm. Ges. Wiss. Prag, Math.-Naturwiss. Cl. 1899(40): 1–8. Google Scholar

  81. J. Velenovský 1922: Reliquiae Mrkvičkanae. — Pragae:  Fr. ŘivnáčGoogle Scholar

  82. F. Verloove 2002: Ingeburgerde plantensoorten in Vlaanderen. — Brussel: Institut voor Natuurbehoud [Mededeling van het Instituut voor Natuurbehoud 20]. Google Scholar

  83. F. Verloove 2005: New records of interesting xenophytes in Spain. — Lazaroa 26: 141–148. Google Scholar

  84. F. Verloove & E. Sánchez Gullón 2008: New records of interesting xenophytes in the Iberian Peninsula. — Acta Bot. Malac. 33: 147–167. Google Scholar

  85. V. Vladimirov & A. Petrova 2009: Senecio inaequidens (Asteraceae): a new alien species for the Bulgarian flora. — Phytol. Balcan. 15: 373–375. Google Scholar

  86. H. E. Weber 1995: Rubus L. — Pp. 284–595 in: G. Hegi (ed.), Illustrierte Flora von Mitteleuropa, ed. 3, 4/2A. Spermatophyta: Angiospermae: Dicotyledones 2(2). — Berlin etc.: Blackwell. Google Scholar

  87. Y. Yang & P. E. Berry 2011 : Phylogenetics of the Chamaesyce clade (Euphorbia, Euphorbiaceae): Reticulate evolution and long-distance dispersal in a prominent C4 lineage. —  Amer. J. Bot. 98: 1486–1503. Google Scholar

  88. K. H. Zahn 1906: Hieracien der Schweiz. — Neue Denkschr. Allg. Schweiz. Ges. Gesammten Naturwiss. 40: 163–728. Google Scholar

  89. K. H. Zahn 1921: Hieracium. Sect. VII Vulgata (Fortsetzung und Schluss) bis Sect. X. Pannosa (Anfang). — In: A. Engler (ed.), Das Pflanzenreich 76. — Leipzig: Engelmann. Google Scholar

  90. K. H. Zahn 1930–1935: Plieracium 2. — In: P. F. A. Ascherson & K. O. P. P. Graebner (ed.), Synopsis der mitteleuropäischen Flora 12(2). — Leipzig: Borntraeger. Google Scholar

© 2015 BGBM Berlin-Dahlem.
Eckhard Von Raab-Straube and Thomas Raus "Euro Med-Checklist Notulae, 4," Willdenowia 45(1), (27 March 2015). https://doi.org/10.3372/wi.45.45113
Published: 27 March 2015
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