86,534 research outputs found
Otto STAPF (1857-1933), ein Oberösterreicher, der in Kew Karriere machte
No full textSpeta, F. (2006): Otto STAPF (1857-1933), ein Oberösterreicher, der in Kew Karriere machte. Linzer biologische Beiträge 38 (1): 217-276, DOI: 10.5281/zenodo.543292
Otto STAPF (1857-1933), ein Oberösterreicher, der in Kew Karriere machte
No full textSpeta, F. (2006): Otto STAPF (1857-1933), ein Oberösterreicher, der in Kew Karriere machte. Linzer biologische Beiträge 38 (1): 217-276, DOI: http://doi.org/10.5281/zenodo.543292
Abb. 7 in Otto STAPF (1857-1933), ein Oberösterreicher, der in Kew Karriere machte
No full textAbb. 7: Lebenslauf von Otto STAPF vom 23.5.1881, der dem Promotionsansuchen beigegeben worden war (Archiv der Universität Wien).Published as part of Speta, F., 2006, Otto STAPF (1857-1933), ein Oberösterreicher, der in Kew Karriere machte, pp. 217-276 in Linzer biologische Beiträge 38 (1) on page 228, DOI: 10.5281/zenodo.543292
Scilla siehei SPETA
No full text<i>Scilla siehei</i> (STAPF) SPETA <p>Tirol: Nordtirol, Inntal, Innsbruck, West-Friedhof, auf Kies verwildert, ca. 580m, 8734/1, 19.03.2004, vid. S. Gewolf.</p> <p> <b>Neu für Tirol</b>. Seit dem bei WALTER et al. (2002) aufscheinenden Fund sind etliche neophytische Nachweise dieser aus SW-Asien stammenden, v.a. auf Friedhöfen häufig anzutreffenden Art aus Österreich publiziert worden. Die bisherigen Angaben stammen aus Wien und dem Burgenland (MELZER & BARTA 2005 und 2007), aus Niederösterreich (MELZER & BARTA 2005, ESSL & STÖHR 2006), aus Oberösterreich (HOHLA 2002 und 2006) und aus Salzburg (SCHRÖCK et al. 2004). Sicherlich folgen in Kürze Meldungen aus den übrigen Bundesländern.</p>Published as part of <i>Stöhr, O., Pilsl, P., Essl, F., Hohla, M. & Schröck, C., 2007, Beiträge zur Flora von Österreich, II, pp. 155-292 in Linzer biologische Beiträge 39 (1)</i> on page 248, DOI: <a href="http://zenodo.org/record/5407540">10.5281/zenodo.5407540</a>
Ebertia Speta
No full text6. Ebertia Speta in Phyton (Horn, Austria) 38(1): 65 (1998). Typus generis:— Ebertia nana (Oyewole) Speta = Urginea nana Oyewole (holotype). Description:—Small bulbous geophyte to ca. 8 cm tall. Bulb hypogeal, ovoid-oblong to subglobose, 2‒3 cm long, with short bulb neck, outer scales membranous and inner bulb scales white. Roots thickened and branched. Leaves 4‒10, hysteranthous, 8‒20 cm long and 1‒3 mm wide, thin, filiform and spreading or linear-lanceolate and erect to arching, green, smooth, glabrous. Inflorescence a short, dense raceme with (1–)3‒6 flowers; peduncle erect, terete, smooth, 1.5‒ 4.5 cm long, greenish to dark purple; pedicels spreading, 1‒4 mm long, glabrous; pedicels of fruits laterally recurved, to 15 mm long. Bracts broadly lanceolate, persistent, lowermost to 6 mm long with distinct flat, decurrent, bifid spur of ca. 1.5 mm long; bracteoles absent. Flowers campanulate, subpatent. Tepals 6, 5‒10 mm long, free to shortly fused at base for ca. 1 mm, lanceolate to oblong, spreading, whitish, pinkish or pale greenish with yellow or hyaline margins, sometimes slightly tinged with dark purple, with distinct dark purple brown longitudinal band on abaxial side, outers sometimes reflexed. Stamens 6, spreading; filaments 3‒4 mm long, white or greenish; anthers oblong, up to 2 mm long, opening by longitudinal slits. Ovary elongate oblong to pyramidal, 3‒4 mm long, greenish, sometimes puberulous near apex, with 10‒15 ovules per locule. Style short, 1‒3 mm long, erect, white, filiform. Capsule ovate to sphaerical, 8‒12 mm long, trigonous with blunt edges in section, mucronate, pale brown. Seeds flattened, dark brown to black, 7‒8 mm long, with membranous wings, uniseriate per locule. Number of species and distribution:— Ebertia is known to include 2 species, occurring disjunctly in Central and West Africa, in Guinea, Sierra Leone, Nigeria and Sudan (Fig. 8). It is restricted to the Guineo-Congolian Region, the Sahelo-Sudanian Subregion and the Eastern Section of the Zambezian Subregion (sensu Takhtajan 1986 and Martínez-Azorín et al. 2023a). The species occurs in frequently burnt grasslands on mountain slopes at elevations of 300‒2000 m (Oyewole 1989, Friis & Vollesen 1999). For further information on Ebertia species see Baker (1898), Oyewole (1989), and Friis & Vollesen (1999). Karyology:—2n=20 (Oyewole 1988, as Urginea pauciflora (Baker) Baker). History, diagnostic characters, and taxonomic relationships:— Urginea pauciflora Baker (1898: 539), not to be confused with the illegitimate U. pauciflora Baker (1901: 786) or Drimia pauciflora Baker (1892: 6), was described by Baker (1898) based on small plants from Sierra Leone (West Africa) possessing hypogeal bulbs, leaves non-coetaneous with flowers, a short peduncle, raceme with 2‒3 campanulate flowers, stamens shorter than tepals and with flattened filaments, and inserted style. Friis & Vollesen (1999) proposed the new name Drimia sudanica Friis & Vollesen for U. pauciflora and extended the range of this species from West Africa (Sierra Leone and Guinea) to southern Sudan. These authors added important characters such as the very short raceme with 4‒6 flowers, lanceolate bracts with a flat, decurrent spur (a character not mentioned by Baker, but matching the type material at Kew herbarium), pedicels 1.5‒2.0 mm long, tepals 5‒7 mm long, shortly connate for ca. 1 mm at the base and spreading, with a dark purple-brown midrib, stamens 3‒4 mm long, filaments spreading, ovary elongate and ca 3 mm long, and very short style. Ripe capsules and seeds were not studied. A related species was described by Oyewole (1989) as Urginea nana Oyewole (1989: 623) from Nigeria, showing small, hypogeal, compact bulbs, filiform erect to spreading leaves that are not coetaneous with flowers, peduncle erect, up to 4 cm long, raceme short and compressed with up to 6 flowers, pedicels reflexed during fruit development, tepals 6‒10 mm long, free, the outers reflexed at anthesis, ovary pyramidal, 3‒4 mm long, style short and erect, capsule ovoid-spherical with mucronate apex, seeds flattened, subellipsoid, 7‒8 mm long, dark brown to black, and uniseriate per locule. The author also illustrated a dehisced capsule showing widely open valves, similar to those found in D. khubusensis P.C.van Wyk & J.C.Manning in Manning & Goldblatt (2018: 120), here considered to belong to Iosanthus. Further, Oyewole (1989) described a considerable morphological variation and three morphotypes in Urginea nana; further studies are needed to improve our understanding of this taxon. Speta (1998b) published Ebertia to include the tropical African taxa U. pauciflora and U. nana, being characterised by the hypogeal compact bulbs, filiform, proteranthous leaves, short peduncle and condensed few-flowered raceme, shortly spurred bracts, straight and patent pedicels, nocturnal, campanulate flowers with tepals shortly connate at base, filaments shorter than tepals, ovary inferior [examination of the type confirms this as erroneous], with 12 ovules per locule, style slightly thickened at the apex, pedicels of ripe capsules laterally recurved, capsules ovoid to globose, and flattened black seeds. The phylogenetic analyses of Pfosser & Speta (1999) place a sample of E. nana as sister to a sample from Senegal named `Thuranthos indicum´ sensu lato, but fitting with Vera-duthiea in the sense of the present work. Pfosser & Speta (2001, 2004) extended the study to include four samples of E. nana (Oyewole 1989: 623) Speta (1998b: 68) from Guinea and Senegal that constituted a well supported clade sister to “ Duthiea ” species (= Vera-duthiea) from Senegal and Botswana. The recent phylogenetic analyses by Martínez-Azorín et al. (2023a) included three samples of Ebertia from Guinea and Senegal and form a strongly supported clade that is sister to Vera-duthiea. Based on the above-mentioned evidence, we accept Ebertia as including E. pauciflora (Baker 1898: 539) Speta (1998b: 68) and E. nana, taxa flowering shortly after grassland fires (Oyewole 1989, Friis & Vollesen 1999). These two species share a small size, non-coetaneous and filiform leaves, short peduncle and condensed, few-flower racemes, subcampanulate flowers with almost free, suberect to slightly spreading tepals, stamens shorter than tepals and included, an ovoid to conical ovary ca. 3 mm long which is sometimes puberulous, and short and erect style of equal length to the ovary. Further, E. nana is unique in the Urgineoideae in having reflexed pedicels that subtend the ripe capsules, since the remaining subfamily members always support ripe capsules on erect to suberect pedicels, except for the northwest African Spirophyllos. Further studies are necessary to compare this character with U. pauciflora. The widely spreading capsule valves and seed morphology in U. nana approach Iosanthus, a genus that is related to the clade comprising Urginea, Spirophyllos, and Indurgia (Martínez-Azorín et al. 2023a). Accepted species:— Ebertia nana (Oyewole) Speta in Phyton (Horn, Austria) 38(1): 68 (1998) ≡ Urginea nana Oyewole in Ann. Missouri Bot. Gard. 76(2): 623 (1989) ≡ Drimia minuta J.C.Manning & Goldblatt in Bothalia 43(1): 77 (2013), nom. nov. ≡ Drimia nana (Oyewole) J.C.Manning & Goldblatt in Edinburgh J. Bot. 60(3): 557 (2004), nom. illeg. [non Drimia nana (Snijman) J.C.Manning & Goldblatt in Bothalia 33(1): 111 (2003)]. Type:— NIGERIA. Ilorin, near the academic area, University of Ilorin, S00/2111 (IUH holo.; FHI iso.). Ebertia pauciflora (Baker) Speta in Phyton (Horn, Austria) 38(1): 68 (1998) ≡ Urginea pauciflora Baker, Fl. Trop. Afr. [Oliver et al.] 7(3): 539 (1898), basionym ≡ Drimia sudanica Friis & Vollesen in Nordic J. Bot. 19(2): 210 (1999), nom. nov. [non Urginea pauciflora Baker in Bull. Herb. Boissier ser. 2, 1: 786 (1901), nom. illeg., nec Drimia pauciflora Baker (1892)]. Type:— SIERRA LEONE. Near Wallia, on the River Scarcies, 11 February 1892, G.F. Scott-Elliot 4580 (K000257328! lecto. designated by Friis & Vollesen in Nordic J. Bot. 19(2): 210. 1999; BM! isolecto.). 7. Fusifilum Raf., Fl. Tellur. 2: 27 (1837) (Figs 21–23). Typus generis:— Drimia physodes (Jacq.) Jessop (lectotype, designated by Deb & Dasgupta in J. Econ. Tax. Bot. 3: 823. 1982). = Physodia Salisb., Gen. Pl.: 37 (1866) ≡ Urginea sect. Physodia (Salisb.) Baker in J. Linn. Soc., Bot. 13: 216 (1873) ≡ Drimia sect. Physodia (Salisb.) J.C.Manning & Goldblatt in Strelitzia 40: 92 (2018). Typus generis:— Physodia pusilla (Jacq.) U.M̧ll.-Doblies (lectotype, designated by Deb & Dasgupta in J. Econ. Tax. Bot. 3: 823. 1982). Description:—Small bulbous geophyte. Bulb hypogeal, ovoid to subglobose, 1‒7 cm in diam., sometimes with short bulb neck, solitary or commonly clump forming, inner scales fleshy, white and compact, outer scales membranous. Roots thickened and branched. Leaves 1‒10, hysteranthous, 3‒15 cm long and 1‒30 mm wide, usually flat, canaliculate, lanceolate, spreading, green, glabrous or papillose. Inflorescence a dense, short or elongated raceme, 1‒8 cm long, with 6‒60(–120) flowers; peduncle erect, terete, smooth or papillose, 4‒15 cm long, greenish to dark purple; pedicels patent-spreading, 8‒30 mm long, glabrous. Bracts lanceolate, small, persistent, lowermost 1‒2 mm long with short spur of ca. 1 mm long; bracteoles absent. Flowers stellate, suberect, diurnal, opening in afternoon. Tepals 6, biseriate, 4‒7 mm long, spreading, white, with distinct greenish to purplish longitudinal band on abaxial side, free to shortly fused at base for less than 1 mm, outers sometimes slightly reflexed. Stamens 6, spreading; filaments 3‒4 mm long, fusiform, narrowed to base and apex, white, with distinct papillae along basal third; anthers oblong, medifixed, to 1 mm long, opening by longitudinal slits. Ovary oblong, truncate to style, 2‒4 mm long, white, with 10‒15 ovules per locule. Style 2‒3 mm long, erect, white, filiform. Capsule ovate to sphaerical, trigonous with blunt edges in cross-section, 6‒12 mm long, pale brown. Seeds subellipsoid, (3–) 4‒8 mm long, flattened with prominent central embryo and wide, flat or incurved wings, dark brown to black, glossy, with sinuous anticlinal testa cell walls. Number of species and distribution:—It includes 17 species, occurring in Southern Africa (Fig. 8) and restricted to the Cape, Karoo-Namib and Uzambara-Zululand Regions, and the Southern Section of the Zambezian Subregion (sensu Takhtajan 1986 and Martínez-Azorín et al. 2023a). For further information on Fusifilum species see M̧ller-Doblies et al. (2001). We preliminarily accept F. magicum as originally circumscribed as belonging to Fusifilum based on its flower morphology (Fig. 23.1). However, its phylogenetic position places two samples of this species in a clade related to Urginea revoluta and Boosia (Martínez-Azorín et al. 2023a). Further studies, including new phylogenetic evidence, are needed to evaluate other alternatives. Karyology:—2n=20 (De Wet 1957, as Urginea depressa Baker). History, diagnostic characters, and taxonomic relationships:— Fusifilum was described to accommodate some species of Urgineoideae having small to medium-sized, subcapitate inflorescence; white stellate, flowers; fusiform and papillate filaments; and white gynoecium. The latter character is unique and diagnostic. The original concept of the genus included species described and illustrated by Jacquin (1795) from Southern Africa and by Ruiz & Pavón (1802) from South America, the latter belonging to Oziroe Rafinesque (1837: 53). However, the current concept of Fusifilum excludes the American taxon, and Deb & Dasgupta (1982) typified the genus on F. physodes (Jacquin 1795: 18) Speta (1998b: 69) (M̧ller-Doblies et al. 2001, Martínez-Azorín et al. 2015). Later, other generic names, such as Physodia Salisbury (1866: 37), were applied to this distinct group of plants. Speta (1998b) accepted Fusifilum to include seven species, and M̧ller-Doblies et al. (2001) presented a taxonomic revision that included 16 species, four from Speta’s (1998b) treatment, one from Tang & Weiglin (2001), 10 as new, and one new combination. Types of their newly described species are still not deposited in most of the studied herbaria and their morphological descriptions are incomplete, which has impeded further taxonomic work in the genus during the last two decades. The phylogenetic analyses of Manning et al. (2004) included four samples considered by them to belong to Fusifilum, although only F. physodes is a true Fusifilum, following circumscriptions of M̧ller-Doblies et al. (2001) and the present work. The supposed polyphyly of Fusifilum, in the sense of Manning et al. (2004), was one of the main reasons offered to justify the lumping of the evidently broad diversity in Urgineoideae in a single, extremely variable Drimia, excluding Bowiea. However, the correct genus adscription of these species does, in fact, dissolve the polyphyly of Fusifilum and support an analytic rather than a synthetic treatment in the subfamily (Martínez-Azorín et al. 2023a) since ‘ F. dregei ’ is a species of Urgineopsis Compton (as accepted in this work) and ‘ F. marginata ’ belongs to Austronea (Martínez-Azorín et al. 2019a) —a genus sister to Fusifilum. The names Fusifilum calcarata and F. marginata sensu Manning et al. (2004) were never formally combined or published prior to 2004. Manning & Goldblatt (2018) described Drimia sect. Physodia, which mostly fits the concept of Fusifilum in this work, but excluding Urginea virens that belongs to Austronea (Martínez-Azorín et al. 2019a). Manning & Goldblatt (2018) placed eight of the species described by M̧ller-Doblies et al. (2001) under their Drimia physodes (Jacquin 1795: 18) Jessop (1977: 300), commenting that those names were not validly published since the types were not deposited following Art. 40.7 of the ICN. However, this interpretation is incorrect, as the Shenzhen Code only recommends that the type material, especially the holotype, should be deposited in a public herbarium or other public collection allowing access and warranting long-term conservation (Art. 7 Rec. 7A1 of the ICN). Therefore, these M̧ller-Doblies names are valid following the current Shenzhen Code, and hence must be accepted. Our field work in Southern Africa over the last decades has enabled us to observe clear morphological differences in support of the acceptance of the species of M̧ller-Doblies et al. (2001). Our phylogenetic analyses show 20 samples of Fusifilum, including several type collections provided by U. & D. M̧ller-Doblies, forming a strongly supported clade sister to Austronea (Martínez-Azorín et al. 2023a), further supporting the acceptance of this genus based on a unique syndrome of morphological characters, biogeography, and phylogenetic relationships. Accepted species and required new combination:— Fusifilum bruce-bayeri U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 479 (2001). Type:— SOUTH AFRICA. Western Cape. Worcester (3319): Worcester West, Polhillia waltersii Nature Reserve, (–CB), elev. 250 m, 15 August 1984, M̧ller-Doblies 84017f (PRE holo.; B, BTU, E, G, GRA, K, M, MO, NAS, NBG, S, W, WIND, Z iso.; ex cult. BTU5931: ibidem. Not deposited in the cited herbaria). Fusifilum capitatum (Hook.f.) Speta in Phyton (Horn, Austria) 38(1): 69 (1998) ≡ Ornithogalum capitatum Hook.f. in Curtis’s Bot. Mag. 89: t. 5388 (1863), basionym (Figs 2.3, 21.3) [non Drimia capitata Baker (1897)] ≡ Urginea capitata (Hook.f.) Baker, Fl. Cap. (Harvey) 6(3): 465 (1897) ≡ Physodia capitata (Hook.f.) U.Müll. -Doblies, J.S.Tang & D.Müll.-Doblies in Feddes Repert. 107(5−6): 520 (1996) (Fig. 22.1). Type:— SOUTH AFRICA. British Kaffraria [part of Eastern Cape today], 1860, Cooper 208 (K000365544! lecto. designated as “holo” by Manning & Goldblatt in Strelitzia 40: 93. 2018; Z-000086255! isolecto.). Fusifilum crenulatum U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 483 (2001) (Fig. 22.2). Type:— SOUTH AFRICA. Northern Cape. Kamiesberg (3018): Koringlandskloof, 1 km on Leliefontein road from Garies / Platbakkies road, (–AC), loamy ground, elev. 1200 m, 12 August 1980, M̧ller-Doblies 80087b (PRE holo.; B, BTU, G, K, M, MO, NAS, NBG, S, WIND, Z iso.; ex cult. BTU4033: ibidem. Not deposited in the cited herbaria). Fusifilum depressum (Baker) U.Müll. -Doblies, J.S.Tang & D.Müll.-Doblies in Feddes Repert. 112(7−8): 480 (2001) ≡ Urginea depressa Baker in Bull. Herb. Boissier ser. 2, 4: 1000 (1904), basionym ≡ Drimia depressa (Baker) Jessop in J. S. African Bot. 43: 297 (1977) (Fig. 22.3). Type:— SOUTH AFRICA. Gauteng. Johannesburg (2628): Transvaal, Modderfontein, (–CB), September 1897, Conrath 687 (Z000027555! lecto. designated here). Note:—The lectotype designation by Jessop in J. S. African Bot. 43: 297 (1977) is not acceptable according to Art. 8.2 Ex. 3 of the Code (see Martínez-Azorín & Crespo 2014; the voucher K000857414! bears a different collection date of 9 October 1898, perhaps erroneously transcribed. In that case it is a true isolectotype, as well as GZU!). Fusifilum emdeorum J.S.Tang & Weiglin in Feddes Repert. 112(7−8): 505 (2001). Type:— SOUTH AFRICA. Western Cape. Worcester (3319): Farm Gevonden, E end of Dutoitskloof, (–CA), elev. 300 m, 22 July 1986, M̧ller-Doblies 86017c (PRE holo.; B, BTU, K, M, MO, NBG, S, WIND, Z iso.; ex cult. BTU6466: ibidem and G, GRA, LI, NAS, W. Not deposited in the cited herbaria). Fusifilum gifbergense U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 479 (2001). Type:— SOUTH AFRICA. Western Cape. Vanrhynsdorp (3118): Snorkfontein, half way up the Gifberg, (–DD), elev. 500−600 m, 16 August 1980, M̧ller-Doblies 80105v (PRE holo.; B, BTU, E, G, K, LI, M, MO, NAS, NBG, P, S, W, WIND, Z iso.; ex cult. BTU4239: ibidem. Not deposited in the cited herbaria). Fusifilum glaucum U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 481 (2001). Type:— SOUTH AFRICA. Western Cape. Vanrhynsdorp (3118): Zandkraal, Gifberg road, 2.7 km S of turn off to Zandkraal, (–DB), elev. 150 m, 16 August 1980 veg., M̧ller-Doblies 80104e (PRE holo.; B, BTU, K, M; ex cult. BTU4201: B, BTU, G, K, LI, M, MO, NAS, NBG, PRE, S, WIND, Z iso. Not deposited in the cited herbaria). Fusifilum hei U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 480 (2001). Type:— SOUTH AFRICA. Western Cape. Montagu (3320): Matjesfontein, Farm Boelhouer (Bullover), 4 km on Keurfontein (Driekop) road, (–BA), elev. 1050 m, 02 August 1986 veg., M̧ller-Doblies 86032a (PRE holo.; B, BTU, K, NAS, S iso; ex cult. BTU6607: ibidem. Not deposited in the cited herbaria). Fusifilum magicum U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 491 (2001) (Fig. 23.1). Type:— SOUTH AFRICA. Western Cape. Beaufort West (3222): Boesmansklip, 2.5 km from N1 to Molteno Pass, (–BC), elev. 900 m, 15 January 1984, M̧ller-Doblies 84129c (PRE holo; B, BTU, K, NBG. Not deposited in the cited herbaria). Fusifilum minus (A.V.Duthie) Speta in Phyton (Horn, Austria) 38(1): 69 (1998) ≡ Urginea minor A.V.Duthie in Ann. Univ. Stellenbosch 6. Sect. A, No. 2, 11 (1928), basionym ≡ Drimia minor (A.V.Duthie) Jessop in J. S. African Bot. 43(4): 306 (1977) ≡ Physodia minor (A.V.Duthie) Salisb. ex U.Müll. -Doblies, J.S.Tang & D.Müll.-Doblies in Feddes Repert. 107(5−6): 520 (1996). Type:— SOUTH AFRICA. Western Cape. Cape Town (3318): Stellenbosch Flats, (–DD), March 1924, Duthie s.n. STE1546 (NBG0197706! lecto. designated as “holo.” by Jessop in J. S. African Bot. 43: 306. 1977); K000257366!, PRE0049735! isolecto.). Fusifilum montanum (A.P.Dold & E.Brink) A.P.Dold, Mart. -Azorín, M.B.Crespo, M.Pinter & Wetschnig comb. nov. ≡ Drimia montana A.P.Dold & E.Brink in Bothalia 36(1): 64 (2006) basionym ≡ Drimia montana A.P.Dold & E.Brink in Taxon 63: 1130 (2014), nom. superfl. ≡ Fusifilum montanum (A.P.Dold & E.Brink) A.P.Dold, Mart. -Azorín, M.B.Crespo, M.Pinter & Wetschnig in Phytotaxa 201(2): 168 (2015), comb. inval. (Figs 2.4, 23.2). Type:— SOUTH AFRICA. Eastern Cape. Fort Beaufort (3226): Groot Winterberg, The Hoek farm, (–AD), elev. 2150 m, 1 January 2004, A.P. Dold 4633 (GRA0000460! lecto. designated here: only the plants in flower and fruit lacking leaves “Pressed in December at time of collection” [though corrected to January by A.P. Dold 08/10/2014; A.P. Dold pers. comm.], which are placed on the upper half of the sheet.). Comments:—In the light of the recentmost proposal by Mosyakin & McNeill (2022) to amend Art. 8 of the ICN, after which the information in the protologue will rule, and considering that the protologue in Dold & Brink (2006) only indicates a single collecting date (01- 01-2004) in the holotype designation, a lectotypification is needed from the mixed type collection GRA0000460. Based on the new considerations, the description made by Martínez-Azorín & Crespo (2014: 1330) and the combination in Martínez-Azorín et al. (2015: 168) are therefore nomenclaturally inoperative, since it is either superfluous or not valid. Fusifilum oliverorum U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 487 (2001). Type:— SOUTH AFRICA. Western Cape. Bredasdorp (3420): Moerasfontein, 1.3 km NW of Skipskop / Bredasdorp road, (–CB), elev. 30 m, 18 August 1984 veg., Oliver & M̧ller-Doblies 84025a (PRE holo.; B, BTU, K, M, MO, NBG, S, WIND, Z iso; ex cult. BTU 6000, 6001, 6002, 6003: ibidem. Not deposited in the cited herbaria). Fusifilum papillosum U.Müll. - Doblies, J.S.Tang & D.Müll. - Doblies in Feddes Repert. 112(7−8): 487 (2001). Type:— SOUTH AFRICA. Northern Cape. Calvinia (3119): Glen Lyon States, SE of Nieuwoudtville, (–AC), elev. 750 m
Chromosomal diversification and karyotype evolution of diploids in the cytologically diverse genus Prospero
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Variations on the Author
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No full textNewspaper article titled "Author Claims Evidence of Second JFK Assassin." The article states that author Richard J. Whalen concluded "that there is circumstantial evidence to support the theory of a second assassin in the shooting of President John F. Kennedy.
Also By The Same Author: AKTiveAuthor, a Citation Graph Approach to Name Disambiguation
No full textThe desire for definitive data and the semantic web drive for inference over heterogeneous data sources requires co-reference resolution to be performed on those data. In particular, name disambiguation is required to allow accurate publication lists, citation counts and impact measures to be determined. This paper describes a graph-based approach to author disambiguation on large-scale citation networks. Using self-citation, co-authorship and document source analyses, AKTiveAuthor clusters papers, achieving precision of 0.997 and recall of 0.818 over a test group of eight surname clusters
John F. Kennedy telegram to Roosevelt
No full textJersey Homesteads (later the Borough of Roosevelt) was established in the 1930s as an agro-industrial cooperative community. It was established specifically for urban Jewish garment workers, many of whom had emigrated from Europe. President John F. Kennedy sent a telegram to the citizens of Roosevelt, New Jersey, apologizing for not being able to attend the memorial dedication in honor of former President Franklin Delano Roosevelt. (Jersey Homesteads became Roosevelt in 1945 in honor of the president.) President Kennedy expressed his gratitude to the people of Roosevelt for constructing the memorial, and commented that it will serve as a constant reminder of Roosevelt's good works
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