196,224 research outputs found
Smithsonian Plant Collections, Guiana Shield: 2002-2012, Karen M. Redden and Kenneth J. Wurdack
Smithsonian Plant Collections, Guiana Shield: 2002–2012, Karen M. Redden and Kenneth J. Wurdack. Part I provides the collector’s notes on trips with maps by date. Part II lists collection localities, with collection number ranges, habitat descriptions, geographic coordinates, and assisting collectors. Part III lists collections in numerical order with identifications and authors. Part IV lists collections ordered by determined name.</p
Miconia amacurensis Wurdack
[1056] Miconia amacurensis Wurdack Acta Bot. Venez. 2: 373 (Wurdack 1967). HERBARIUM DATA (FG). — 2 collections at CAY. Sel. exs.: P.A. Sagot 987, Nov. 1856 (P [P05206288]). SIZE. — Up to 16 m tall (Wurdack et al. 1993).Published as part of Molino, Jean-François, Sabatier, Daniel, Grenand, Pierre, Engel, Julien, Frame, Dawn, Delprete, Piero G., Fleury, Marie, Odonne, Guillaume, Davy, Damien, Lucas, Eve J. & Martin, Claire A., 2022, An annotated checklist of the tree species of French Guiana, including vernacular nomenclature, pp. 345-903 in Adansonia (3) (3) 44 (26) on page 562, DOI: 10.5252/adansonia2022v44a26, http://zenodo.org/record/745877
Mg-enriched ovipositors as a possible adaptation to hard-skinned fruit oviposition in Drosophila suzukii and D. subpulchrella
The globally spreading pest Drosophila suzukii and its relative D. subpulchrella (Diptera: Drosophilidae) possess an elongated ovipositor with enlarged bristles which is associated with their ability to oviposit into hard-skinned fruits. Other species of the genus ovipositing in damaged fruit and decaying material have blunt ovipositors with small bristles. In insects, the ability to cut or penetrate hard substrates may, apart from the intrusion organ’s shape, also depend on the incorporation of metals in the cuticle. Here, we hypothesized that D. suzukii and D. subpulchrella have more metal-enriched ovipositors than the closely related D. melanogaster, D. biarmipes and D. mimetica (all unable to attack hard-skinned fruit). Energy-dispersive X-ray spectrometry showed that two alkaline earth metals, magnesium (Mg) and calcium (Ca), occur in the ovipositors of Drosophila, providing the first evidence of metal-enriched ovipositors in Diptera. Mg occurred in all individuals of D. suzukii and D. subpulchrella but in no individuals of the other species. Mg was only detected in the ovipositor bristles, with up to about 0.3%wt, suggesting that these structures play an important role in drilling fruit skin. Ca, on the other hand, occurred rarely and in traces across most species, and was detected both in and out of bristles. We suggest that Mg-enrichment may represent an adaptation to hard-skinned fruit oviposition, and, together with its modified ovipositor morphology, may further explain why D. suzukii is so successful as an invader
Meriania acida Wurdack, Phytologia
<p> <b>1.</b> <i>Meriania acida</i> (Markgr.) Wurdack, Phytologia 35(1): 5 (1976).</p> <p> Basionym: <i>Graffenrieda acida</i> Markg., Notizbl. Bot. Gart. Berlin-Dahlem 13(119): 462 (1937).</p> <p> Type:— <b>PERU. Cajamarca:</b> Prov. Cutervo, Tambillo, 26 Aug 1878 (fl.), <i>A. Raimondi 3341</i> (lectotype, designated here: USM! [accession no. 1629g]; isolectotypes: USM! [accession nos. 1629a, 1629b, 1629c, 1629d, 1629e, 1629f, 1629h], US!-fragment [barcode 001201396]). Remaining syntypes:— <b>PERU. Cajamarca:</b> Prov. Cutervo, Tambillo, 26 Aug 1878 (fl.), <i>A. Raimondi 3695</i> (fl.) (USM! [accession no. 1629l]), <i>A. Raimondi 3813</i> (USM! [accession nos. 1629m, 1629n, 1629ñ]), same locality and date (ster.), <i>A. Raimondi 4844</i> (USM! [accession no. 1629j]), same locality and date (fl.), <i>A. Raimondi 6126</i> (USM! [accession no. 1629m]). <b>COLOMBIA. Antioquia:</b> S. Augusto, 25 Dec 1879, <i>Kalbreyer 1293</i> (not located). (Figure 8).</p> <p> <b>Comments:—</b> <i>Meriania acida</i> is only known in Peru from the original material collected by A. Raimondi in 1878. It is characterized by its calyptrate calyces without dorsal projections (Fig. 8E) and campanulate, reddish-orange corollas. In Peru there are three other species with calyptrate calyces (<i>M. escalerensis</i>, <i>M. sessilifolia</i> and <i>M. tomentosa</i>). However, <i>M. escalerensis</i> and <i>M. sessilifolia</i> have spreading, deep pink to reddish-purple corollas. In addition, <i>M. escalerensis</i> has calyces with circumscissile dehiscence (vs. irregular in <i>M. acida,</i> Fig. 8E) and stamen connectives with blunt ascending dorsal appendages (vs. absent). On the other hand, <i>M. sessilifolia</i> shares with <i>M. acida</i> the calyces with irregular dehiscence but the former is clearly distinguishable by its sessile leaves [vs. clearly petiolate, (1.5–) 2.2–3.4 cm long]. The Peruvian species most similar to <i>M. acida</i> is <i>M. tomentosa</i>, but they can be differentiated by the petal length (9–10 mm long vs. 20–24 mm long) and the shape of the descending dorso-basal appendages of the stamen connectives (acute vs. blunt).</p> <p> Based on a collection made in Amazonas (<i>Wurdack 1054</i>), Wurdack (1964, 1976) considered <i>M. acida</i> to be closely related to <i>M. denticulata</i> (Gleason) Wurdack, from Ecuador, because both share subcalyptrate calyces and small dorsal projections on the calyx. However, after a detailed analysis we recognized <i>Wurdack 1054</i> to be an undescribed species, and proposed <i>M. juanjil</i> (Fernandez-Hilario <i>et al.</i> 2022). <i>Meriania acida</i> is easily distinguishable from <i>M. juanjil</i> by its calyptrate calyx without dorsal projections (vs. subcalyptrate with acute dorsal projections), leaf blades 5–8 cm wide (vs. 2.7–3 cm wide) and petals 9–10 mm long (vs. 11–13.5 mm long).</p> <p> <b>Nomenclatural notes:—</b> Markgraf (1937) cited in the protologue five Peruvian specimens (<i>Raimondi 3341</i>, <i>3695</i>, <i>3813</i>, <i>4844</i> and <i>6126</i>) and one Colombian specimen (<i>Kalbreyer 1293</i>), so these specimens must be considered as syntypes conforming with Art. 9.6 of the ICN (Turland <i>et al.</i> 2018). The A. Raimondi collection housed in USM corresponds to the specimens that were sent on loan to Berlin in 1926 (Anonymous 1939, 1942), so they may have been seen by F. Markgraf. According to Art. 9.3 and 9.12 of the ICN (Turland <i>et al.</i> 2018), we chose <i>Raimondi 3341</i> for lectotypification, because this specimen has the highest number of fertile sheets (duplicates).</p> <p> <b>Distribution and phenology:—</b> <i>Meriania acida</i> is apparently restricted to northern Peru and only present in the department of Cajamarca (Fig. 9). Markgraf (1937) cited one Colombian specimen in the protologue of <i>M. acida</i>. However, none of the species currently recognized for Colombia (see Mendoza-Cifuentes 2021) matches the concept we used here for <i>M. acida</i>. Although the original material collected by A. Raimondi does not give details of its habitat, <i>Meriania acida</i> probably grows in montane forest relicts. It has been collected in flower in August.</p> <p> <b>Specimens examined:—</b> <b>PERU. Cajamarca:</b> Prov. Cutervo, Tambillo, 26 Aug 1878 (ster.), <i>A. Raimondi 3536</i> (USM!), same localty and date (ster.), <i>A. Raimondi 6240</i> (USM!), same localty and date (ster.), <i>A. Raimondi 6319</i> (USM!).</p>Published as part of <i>Fernandez-Hilario, Robin, Goldenberg, Renato & Michelangeli, Fabián A., 2023, A synopsis of Meriania (Melastomataceae: Merianieae) in Peru, pp. 1-101 in Phytotaxa 602 (1)</i> on pages 14-15, DOI: 10.11646/phytotaxa.602.1.1, <a href="http://zenodo.org/record/8141984">http://zenodo.org/record/8141984</a>
Meriania amischophylla Wurdack, Phytologia
<p> <b>2.</b> <i>Meriania amischophylla</i> Wurdack, Phytologia 48(3): 238 (1981).</p> <p> Type:— <b>PERU. Loreto [Huánuco]:</b> Prov. Coronel Portillo, Dist. Padre Abad, la cumbre de la Divisoria, 1500–1600 m, 6 Feb 1978 (fl.), <i>J. Schunke V. 9842</i> (holotype: US! [barcode 00120355]; isotypes: AAU!, F! [accession no. 2010208], MO! [accession no. 2796540], NY! [barcode 00228949], U! [barcode U0282674], USM! [accession no. 88597]). (Figure 10).</p> <p> <b>Comments:—</b> <i>Meriania amischophylla</i> is easily distinguishable from other Peruvian species by its subsessile leaves (petioles up to 3 mm long) (Fig. 10B), calyces with regular dehiscence (Fig. 10D), spreading, reddish-purple corollas and antesepalous stamen connectives with laterally expanded descending dorso-basal appendages and dorsal appendages as mere humps (Fig. 10G). Laterally expanded dorso-basal appendages have only been observed in six other Peruvian species (<i>M. hirsuta</i>, <i>M. sumatika</i>, <i>M. vargasii</i>, <i>M. vasquezii</i>, <i>M. vilcabambensis</i> and <i>M. weberbaueri</i>). Within this group, <i>M. amischophylla</i> is more closely related to <i>M. weberbaueri</i>, with which it shares spreading, fuchsia to reddish-purple corollas and stamen connectives without ascending dorsal appendages. However, <i>M. amischophylla</i> differs from <i>M. weberbaueri</i> by its subsessile leaves (vs. petioles 1.3–5.1 cm long) and distinctly suprabasal secondary veins (vs. basal to slightly suprabasal). <i>Meriania sumatika</i>, <i>M. vargasii</i> and <i>M. vilcabambensis</i> have stamen connectives with ascending dorsal appendages, <i>M. vasquezii</i> has calyces with irregular dehiscence, and <i>M. hirsuta</i> has campanulate, deep red corollas.</p> <p> Sessile or subsessile leaves are unusual characters in the Andean species of <i>Meriania</i>, occurring only in <i>M. amischophylla</i>, <i>M. amplexicaulis</i> Wurdack, <i>M. mexiae</i> Wurdack and <i>M. sessilifolia</i>. <i>Meriania amplexicaulis</i> (Ecuador) is the most closely related to <i>M. amischophylla</i> due to its similar indumentum and calyx with regular dehiscence and dorsal projections. However, the former differs by its petals 16–18 cm long (vs. 19–32 cm), stamens with connectives prolonged below the thecae (vs. not prolonged) and antesepalous stamen connectives with ascending appendages (vs. a mere hump).</p> <p> <b>Distribution and phenology:—</b> <i>Meriania amischophylla</i> is endemic to Peru and restricted to the Cordillera La Divisoria in the Huánuco-Ucayali border, and grows in montane forests at 1500–1600 m (Fig. 11). It has been collected in flower in February and April.</p> <p> <b>Specimens examined:—</b> <b>PERU. Huánuco:</b> Prov. Leoncio Prado, Dist. Hermilio Valdizán, la Divisoria, carretera a Pucallpa, 1600 m, 24 Apr 1980 (fl.), <i>J. Schunke V. 11374</i> (NY!, US!).</p>Published as part of <i>Fernandez-Hilario, Robin, Goldenberg, Renato & Michelangeli, Fabián A., 2023, A synopsis of Meriania (Melastomataceae: Merianieae) in Peru, pp. 1-101 in Phytotaxa 602 (1)</i> on pages 16-17, DOI: 10.11646/phytotaxa.602.1.1, <a href="http://zenodo.org/record/8141984">http://zenodo.org/record/8141984</a>
Miconia sandemanii Wurdack from Colombia collected by Z. Restrepo #5739
File Name: TOLI-23032-EST-04-7-A1-30.jpg
CÓDIGO FOTO: TOLI-23032-EST-04-7-A1-30-
Fotografía: SI
Nº TOLI: TOLI-23032
PARCELA: EST-04
CÓDIGO: 7-A1-30
Nº COLECTA: 5739
NUEVOS COLECTORES: Wilmar López Oviedo
COLECTORES: Z. Restrepo
Nº MUESTRAS MONTADAS: 1
Homologación: Homologado
Nueva fecha del evento : 19/12/2018.
Fecha del evento: 12/09/2014.
Proyecto : Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana
Hábitat: Bosque húmedo montano (bh-M)
Continente: SA
Pais: Colombia
Estado/Provincia: Quindío
Municipio: Salento
Localidad: Reserva Natural Estrella de agua
Elevación minima en metros: 3525
Elevación maxima en metros: 3725
Latitud: 4.616
Longitud original: -75.423
datum geodésico: WGS 84
Latitud decimal: 4.616
Longitud decimal: -75.423
Identificado por: Heriberto David, Humberto Mendoza & J.S. Murillo
Fecha de identificación: 22/01/2019.
Familia antigua: Melastomataceae
Especie antigua: Miconia sandemanii Wurdack
Nombre cientifico: Miconia sandemanii Wurdack
Reino: Plantae
Filo: Magnoliophyta
Clase: Equisetopsida
Orden: Myrtales
Familia nueva: Melastomataceae
Género nuevo: Miconia
especie nueva: sandemanii
Autoría del nombre científico: Wurdack
: Melastomataceae
genero herbario: Miconia
especie herbario: sandemanii
Especie de herbario para TNRS: Miconia sandemanii
Especie corregida herbario y desde TNRS: Miconia sandemanii
Familia corregida desde TNRS: Melastomataceae
: 2147</p
Meriania tomentosa Wurdack, Phytologia
30. Meriania tomentosa (Cogn.) Wurdack, Phytologia 35(1): 4 (1976). Basionym: Centronia tomentosa Cogn., Bull. Acad. Roy. Sci. Belgique ser. 3, 14: 943 (1887). Type:— ECUADOR: Ad margines sylvarum primaev in Andibus central aequadorensibus rara, 3000 m, 1876 (fl.), E. André 4475 (lectotype, designated by Wurdack 1980: BR! [barcode 000005187867]; isolectotypes:, CAS! [barcode 0001923], K! [barcodes K000329483, K000329484], NY! [barcode 00221501]). (Figures 63–64). Rhexia excelsa Bonpl., in Humdoldt & Bonpland, Monogr. Melast. 2: 90, t. 34 (1813). Osbeckia excelsa (Bonpl.) Spreng., Syst. Veg. 2: 312. 1825. Graffenrieda excelsa (Bonpl.) DC., Prodr. 3: 106 (1828). Brachycentrum excelsum (Bonpl.) Meissn., Pl. Vasc. Gen. 2: 81 (1838). Centronia excelsa (Bonpl.) Triana, Trans. Linn. Soc. London 28(1): 70, t. 5 (1871) [1872]. Type:— ECUADOR: Loxa, 1852 (fl.), A. Bonpland 3335 (lectotype, first step designated by Wurdack 1980, second step designated by Mendoza-Cifuentes 2021: P! [barcode P00136435]; isolectotypes: F!-fragment [accession no. 937280], P! [barcode P00136436]). Centronia tunguraguae S.F.Blake, Proc. Biol. Soc. Washington 35: 118 (1922). Type:— ECUADOR. Tungurahua: Pondoa, on slopes of Mt. Tungurahua, 2745 m, 10 Mar 1921 (fl.), W. Popenoe 1296 (holotype: US! [barcode 00120322]). Centronia peruviana J.F.Macbr., Publ. Field Mus. Nat. Hist., Bot. Ser. 13(4/1): 327 (1941). Type:— PERU. Huánuco: Carpish, banks of a mountain stream, 2850 m, 09 Nov 1938 (fl.), H.E. Stork & O.B. Horton 9928 (holotype: F! [accession no. 1052336]). Comments:— Meriania tomentosa is the second most widely distributed Meriania species in Peru, and it is recognisable by its calyptrate calyces with irregular dehiscence and without dorsal projections, campanulate, reddish-orange corollas, isomorphic stamens, and cream anthers. In Peru there are three other species with calyptrate calyces (M. acida, M. escalerensis and M. sessilifolia), and two with subcalyptrate calyces (M. juanjil and M. vasquezii). Within these groups only M. acida shares similar calyces and corollas with M. tomentosa. However, M. acida has smaller flowers than M. tomentosa, hypanthia ca. 4.5 mm long vs. 8.5–9 mm long and petals 9–10 mm vs. 20–24 mm long. The original material of M. tomentosa exhibits indumentum covering the entire abaxial leaf blades, short trichomes on the hypanthium and calyx, linear bracteoles, and calyptrate calyces with a prolonged apiculum. Although most of the Peruvian specimens have the same indumentum on the leaves and shape of the bracteoles (Fig. 64B), there is variability among populations. The calyx apices vary from acute to moderately apiculate. Also, most specimens distributed from the department of Amazonas to Huánuco (e.g., Wurdack 1661) show denser indumentum and longer trichomes than the typical form (Fig. 63A). On the other hand, some specimens from the department of Amazonas (e.g., Fernandez-Hilario et al. 1905) have broadly elliptic bracteoles, even completely covering the flower buds (Fig. 63D). In the department of Pasco there are two clearly distinguishable forms, the former (e.g., Michelangeli et al. 2884) has ferrugineous tomentose indumentum evenly covering abaxial leaf blades, and the latter (e.g., Cárdenas & Francis 450) has setulose indumentum sparsely to moderately covering the abaxial leaf blades. Although we have been able to find these different forms within M. tomentosa, in sterile or fruiting specimens is not possible to identify them. This is because it is necessary to examine the calyces and bracteoles, which are usually early deciduous. For this reason, for the moment we have chosen to consider all Peruvian examined specimens under Meriania tomentosa s.l. Nomenclatural notes:— Cogniaux (1887) cited André 4473 as type in the protologue of C. tomentosa but without indicating any herbarium, so it must be considered as a syntype conforming with Art. 9.6 of the ICN (Turland et al. 2018). Mendoza-Cifuentes (2021) erroneously chose as lectotype the sheet K000329483 because, according to Art. 9.10 and 9.19 of the ICN (Turland et al. 2018), we must consider that Wurdack (1980) made an inadvertent lectotypification of C. tomentosa when he wrote “ André 4475 (BR, holotype) ” in his treatment of Melastomataceae for the Flora of Ecuador. Humboldt & Bonpland (1813) did not cite any specimens in the protologue of R. excelsa but the specimen Bonpland 3335 is original material because it is associated with the taxon, and so it must be considered as a syntype conforming with Art. 9.4 and 9.6 of the ICN (Turland et al. 2018). According to Art. 9.10 of the ICN (Turland et al. 2018), we have to consider that Wurdack (1980) made an inadvertent lectotypification (first-step) of R. excelsa when he wrote “ Bonpland 3335 (P, holotype) ” in his treatment of Melastomataceae for the Flora of Ecuador. However, there are two sheets of Bonpland 3335 housed in P. Therefore, when Mendoza-Cifuentes (2021) chose the sheet K000329439 as the lectotype he made a second-step lectotypification, conforming with Art. 9.17 (Turland et al. 2018). Distribution and phenology:— Meriania tomentosa is widely distributed in the Andes from Venezuela to southern Peru, and occurs from the department of Amazonas to Cusco in montane forests at 2100–3300 m (Fig. 38). It has been collected in flower almost all year round except in January and March, and in fruit almost all year round except in January, May, November and December. Specimens examined:— PERU. Amazonas: Prov. Bongará, Dist. Florida, desde toma de agua en San Lorenzo hacia CP Vista Alegre, 2840 m, 05°48’17.71”S, 78°01’36.70”W, 17–18 Feb 2020 (fl.), R . Fernandez-Hilario et al. 1905 (HOXA!, KUELAP!, MOLF!, NY!, UPCB!), trocha rumbo a CP Perlamayo, 2320 m, 05°47’10”S, 77°54’49”W, 30 Aug 2022 (fl. Bud, fr.), R . Fernandez-Hilario et al. 2274 (MOLF!); Dist. Jumbilla, Along road to Tialango, 2100 m, 05°52’31”S, 76°46’36”W, 04 Nov 2012 (fl.), H . van der Werff et al. 25013 (HOXA!, HUT!, NY!); Dist. Pomacochas, Caserío San Lorenzo, 2800–3500 m, 05°48’25.76”S, 78°00’25.13”W, 28–31 Dec 2011 (fl.), L . Dávila 2180 (UNC!); Dist. Yambrasbamba, Ruta desde CP La Florida hacia finca de Don Ilario, 2150 m, 05°40’17.71”S, 77°56’58.73”W, 12 Nov 2020 (fl.), R . Fernandez-Hilario et al. 2070 (HOXA!, MOLF!, NY!, UPCB!). Prov. Chachapoyas, Middle slopes of Cerro Yama-uma (Cerro Carán) above Taulia, 4–8 km south-southeast of Molinopampa, 2700–3000 m, 11 Aug 1962 (fl.), J . Wurdack 1661 (F!, NY!, P!, US!, USM!); Dist. Leymebamba, alrededor de la laguna de Los Cóndores, parte sur, 2500–2700 m, 06°51’05.28”S, 77°46’25.61”W, 16 Aug 1998 (fl.), V . Quipuscoa et al. 1267 (F!, NY!). Cajamarca: Prov. Chota, Dist. Chadín, CP La Palma, 2530–2707 m, 06°27’12.67”S; 78°24’31.63”W, 24 Nov 2013 (fl.), L . Dávila 2705 (UNC!); Dist. Paccha, Rejo pampa, 2450 m, 21 Jul 1993 (fl.), J . Sánchez 826 (CPUN!, F!). Prov. Hualgayoc, Dist. Chugur, Sector Las Quinas, Ramírez, El Chencho, 3186 m, 06°41’19.44”S; 78°42’44.68”W, 01–02 Sep 2018 (fl.), L . Dávila 3856 (UNC!). Prov. San Miguel, Bosque natural de Quellahorco, al noreste de la localidad de Tongod, 2700 m, 14 Sep 1991 (fl., fr.), I . Sánchez V. & A. Briones 5788 (CPUN!, F!, NY!, UNC!, US!). Prov. Santa Cruz, Dist. Pulán, El Progreso, 2700 m, 31 Jan 2006 (fl. bud), L . Santa Cruz 184 (USM!), 04 Sep 2006 (fl.), L . Santa Cruz 560 (USM!), Chilal, 2700 m, 04 Sep 2006 (fl.), L . Santa Cruz 605 (USM!), 31 Jul 2007 (fl.), L . Santa Cruz 1964 (USM!), La Zaina, 2700 m, 04 Sep 2006 (fl., fr.), L . Santa Cruz 611 (USM!), Sector Pampa Verde, 2920 m, 06°48’6.19”S; 78°54’28.05”W, 16 Oct 2004 (fl.), G . Iberico et al. 950 (CPUN!, UNC!), Sector San Pedro, 3300 m, 05 Jun 2004 (fl.), G . Iberico & L. Dávila 606 (UNC!). Cusco: Prov. La Convención, Dist. Huayopata, Inkatambo, 2630 m, 13°04’07”S, 72°26’49”W, 24 Apr 2007 (fl.), L . Valenzuela 9551 (CUZ!), Incatambo, quebrada Curcur, 2490–2570 m, 13°04’05”S, 72°26’49”W, 21 Nov 2004 (fl.), L . Valenzuela et al. 4477 (CUZ!); Dist. Santa Ana, Tunquimayo, 2800 m, 13°03’S, 72°56’W, 13 Jun 2003 (fr.), E . Suclli & V. Chama 965 (CUZ!, NY!), 2000–2200 m, 12°54’34”S, 72°48’36”W, 20 Oct 2002 (fl.), L . Valenzuela et al. 742 (CUZ!); Dist. Quellouno, Lacco, 2741 m, 12°36’44”S, 72°14’37”W, 16 Jun 2006 (fr.), L . Valenzuela et al. 6896 (NY!, USM!); Dist. Vilcabamba, frente a Yupancca, 2560–2640 m, 13°03’15”S, 72°55’59”W, 03 Jun 2002 (fl.), W . Galiano et al. 4298 (CUZ!, NY!). Prov. Paucartambo, EB Wayqecha, 3000 m, 13°10’S, 71°35’W, Mar 2010 (fr.), P . Chambi s.n. (USM!). Prov. Quishpicanchi, Dist. Marcapata, Sitio Culebrayoc, marca 1550 m en la trocha, 2463 m, 13°29’41.2”S, 70°53’16.2”W, 05 Jun 2012 (fr.), F . A. Michelangeli et al. 1799 (NY!, USM!), Comunidad de Unión Arasa, 2150 m, 13°29’40.92”S, 70°52’23.16”W, 26 Apr 2011 (fr.), J . Wells & P. Centeno 980 (USM!). Huánuco: Prov. Huánuco, Dist. Chinchao, Carpish, 2750 m, 09 Sep 1948 (fl. bud), R . Scolnik 1075 (NY!), ca. 47 km NNE of Huánuco on road to Tingo María, just below the Carpish pass, 2500–2600 m, 14 Jul 1981 (fl.), M . Dillon 2602 (F!), Trail from S entrance of Carpish tunnel to crest of ridge, 2740 m, 27 Feb 1978 (fr.), J . Luteyn & M. Lebron-Luteyn 5477 (NY!), West side of Carpish pass, 2800 m, 22 Oct 1959 (fl.), B . Maguire & C. Maguire 44432 (F!, NY!, US!). Prov. Pachitea, above La Molina near Panao, 12 Sep 1940 (fl.), E . Asplund 13691 (US!). Junín: Prov. Chanchamayo, Dist. San Ramón, Puyu Sacha, 2500 m, 11°05’46”S; 75°26’05”W, 01–11 Apr 2021 (fl.), R . Villanueva-Espinoza 546 (MOLF!). Pasco: Prov. Oxapampa, Cordillera Yanachaga, road over shoulder of Cerro Pajonal to Villa Rica drainage, 12 km SE of Oxapampa, 2300–2500 m, 10°35’S, 75°20’W, 09 Oct 1982 (fl.), R . Foster & D. Smith 9072 (F!, NY!, US!, USM!); Road to Chacos, 2400–2700 m, 10°35’S, 75°06’W, 17 Jul 2003 (fl.), H . van der Werff et al. 18569 (NY!); Dist. Huancabamba, PN Yanachaga Chemillén, la Colmena-trocha Erica, 2300 m, 10°26’37”S, 75°26’15”W, 22 Aug 2008 (fl., fr.), L . Valenzuela et al. 11612 (HOXA!, NY!, USM!), PN Yanachaga Chemillén, sector Quebrada Yanachaga, 2265 m, 10°23’45”S, 75°28’55”W, 19 Aug 2004 (fl.), R . Vásquez et al. 30405 (HOXA!, NY!), de amortiguamiento del PN Yanachaga Chemillén, 2407 m, 10°23’38”S, 75°28’36”W, 20 Sep 2004 (fl.), J . Perea & J. Mateo 1794 (HOXA!, NY!), Fundo Osobamba. PN Yanachaga Chemillén, 2243 m, 10°23’34.7”S, 75°28’28.1”W, 25 Jun 2016 (fl.), L . Valenzuela et al. 30448 (USM!), PN Yanachaga Chemillén, Quebrada Yanachaga, 2420 m, 10°23’21.6”S, 75°28’20.1”W, 20 Feb 2018 (fr.), F . A. Michelangeli & S. Riva 2973 (HOXA!, USM!), Sector Oso Playa. Camino a la parcela Oso Playa, 2565 m, 10°19’05”S, 75°36’28”W, 25 Jun 2006 (fl.), L . Cárdenas et al. 469 (CUZ!), Sector Oso Playa, Trocha a la parcela Oso Playa, 2370–2475 m, 10°19’20”S, 75°36’06”W, 24 Jun 2006 (fl.), L . Cárdenas & R. Francis 450 (HOXA!, USM!), Sector Oso Playa, margen izquierda del río, 2370–2475 m, 10°19’20”S, 75°36’06”W, 17 Jun 2006 (fl.), L . Cárdenas et al. 350 (MO!); Dist. Oxapampa, Chacos “Rincón Chacos”, proyecto Apícola, 2750 m, 10°37’25”S, 75°17’43”W, 23 Jul 2010 (fl.), R . Rojas et al. 7361 (HOXA!, NY!), PN Yanachaga Chemillén, cercanías del refugio El Cedro, 2440–2500 m, 10°32’S, 75°21’W, 17 Aug 2002 (fl., fr.), A . Monteagudo et al. 3701 (HOXA!, NY!, USM!), same locality and date (fl., fr.), 4429 (HOXA!, MOLF!, NY!, USM!), PN Yanachaga Chemillén, flanco oriental del valle de Palcazu, a 20 minutos del 2720 m, 10°31’56”S, 75°20’54”W, 19 Oct 2006 (fl.), A . Monteagudo & R. Francis 12900 (HOXA!, NY!), PN Yanachaga Chemillén, Sector San Alberto, 2450 m, 10°32’43”S, 75°21’30”W, 14 Mar 2019 (fr.), R . Vásquez et al. 43050 (HOXA!), PN Yanachaga Chemillén, sector San Alberto, alrededores del refugio El Cedro, 2240 m, 10°32’42.4”S, 75°21’04.3”W, 22 Mar 2016 (fr.), F . A. Michelangeli et al. 2750 (NY!, USM!), PN Yanachaga Chemillén, sector San Alberto, camino del refugio El Cedro al 2420–2700 m, 10°32’43”S, 75°21’30”W, 03 Oct 2007 (fl., fr.), L . Hernani & A. Peña 383 (HOXA!, NY!, USM!), PN Yanachaga Chemillén, sector San Alberto; claro alrededor del refugio El Cedro, 2415 m, 10°32’43.2”S, 75°21’29.8”W, 20 Jul 2017 (fl. bud, fr.), F . A. Michelangeli et al. 2884 (HOXA!, USM!), Sector San Alberto, camino al 2400–2600 m, 10°32’43”S, 75°21’30”W, 15 Aug 2006 (fl., fr.), L . Cárdenas et al. 693 (CUZ!, F!, HOXA!, MO!, MOLF!, NY!), Sector San Alberto. Cercano al Refugio, 0.5 km, 2468 m, 10°32’45”S, 75°21’24”W, 18 Aug 2006 (fl.), L . Cárdenas et al. 733 (CUZ!), same locality and date (fl.), 734 (HOXA!), Sector San Alberto. Zona superior al refugio aprox. 4 km, 2878 m, 10°31’45”S, 75°21’08”W, 12 Aug 2006 (fl.), L . Cárdenas et al. 661 (CUZ!), same locality and date (fl.), 669 (HOXA!, MO!, USM!), de amortiguamiento PN Yanachaga Chemillén, parte media de la quebrada San Luis, 2200–2350 m, 10°33’55”S, 75°20’43”W, 18 Sep 2007 (fl., fr.), A . Monteagudo et al. 15094 (HOXA!, MOLF!, NY!). Piura: Prov. Huancabamba, Loma Redonda (Sapalache-Chinguela), 2400 m, 15 Sep 1981 (fl., fr.), A . Sagástegui et al. 10188 (HUT!, NY!, US!); El paso de Huascar Rey (límite entre Dp. De Piura y Cajamarca, ruta Huancabamba a Tabaconas), 2700 m, 11 Jul 1961 (fl.), C . Friedberg 322 (P!, US!, USM!); Dist. El Carmen de la Frontera, Carretera Sapalache-Cerro Chingelas, 9.5 km después de Sapalache, 3035 m, 05°08’23.6”S, 79°23’45.4”W, 03 Sep 2016 (fr.), F . A. Michelangeli et al. 2620 (NY!, USM!), same locality and date (fr.), 2623 (NY!, USM!). Prov. Morropón, Dist. Chalaco, Bosque Mijal, 2900 m, 30 Aug 2004 (ster.), A . Córdova 512 (MOLF!). San Martín: Prov. Huallaga Dist. Bolivar, Surrounding “Pampa Hermosa” around old Chacha and Inca settlement, 2400 m, 06°59’32”S, 77°39’16”W, 24 May 2011 (fl), R . Bussmann et al. 17068 (F!, MO!, NY!, US!), same locality and date, 07°02’07”S, 77°40’29”W, (fl.), R . Bussmann et al. 17069 (F!, MO!, NY!, US!). Prov. Mariscal Cáceres, Near Mirador, Río Abiseo National Park, 3000–3100 m, 14 Jul 1988 (fl.), B . León 2175 (US!); Dist. Huicungo, ACP Los Chilchos, borde de la Laguna de los Condores, 2870 m, 06°51’07”S, 77°42’03”W, 27 Jun 2022 (fl.), F . A. Michelangeli et al. 3206 (NY!, USM!).Published as part of Fernandez-Hilario, Robin, Goldenberg, Renato & Michelangeli, Fabián A., 2023, A synopsis of Meriania (Melastomataceae: Merianieae) in Peru, pp. 1-101 in Phytotaxa 602 (1) on pages 79-80, DOI: 10.11646/phytotaxa.602.1.1, http://zenodo.org/record/814198
Meriania vargasii Wurdack, Phytologia
32. Meriania vargasii Wurdack, Phytologia 13(2): 72 (1966). Type:— PERU. Cusco: Prov. La Convención, Hacienda Guayanay, 1800 m, 15 May 1960 (fl.), C. Vargas 13240 (holotype: US! [barcode 00120390]; isotype: CUZ!). (Figure 66). Comments:— Meriania vargasii is related to a group of Peruvian species (M. amischophylla, M. sumatika and M. weberbaueri) that share densely tomentose to villose hypanthia and calyces, calyces with claw-shaped dorsal projections (Fig. 66E), spreading, fuchsia to reddish-purple corollas, and antesepalous stamen connectives with laterally expanded descending dorso-basal appendages (Fig. 66F). However, M. amischophylla has subsessile leaves (vs. petiolate in M. vargasii) and M. weberbaueri has inflorescences with flowers in (3–)4–6(–7)-flowered umbels in the branchlet ends ( vs. in regular dichasia in M. vargasii). On the other hand, some specimens of M. sumatika have been erroneously identified as M. vargasii, but the former differs by its 10-costate hypanthia (vs. terete in M. vargasii), petals 46–55 mm long (vs. 20–24 mm long) and anthers 14–16 mm long (vs. 9–12 mm long). Meriania boliviensis Cogn., endemic to Bolivia, is related to M. vargasii by sharing similar indumentum, dorsal projections on the calyces, and petal length. Nevertheless, M. vargasii is easily differentiated by its petioles 0.8–1.5 cm long (vs. 1.1–4.4 cm long in M. boliviensis) and venation with the innermost pair of secondary veins distant 0.6–1.7 cm from the base of the leaf blades (vs. 0.9–3.9 cm). All examined specimens have conspicuous claw-shaped dorsal projections on the calyces, except Vargas 10644 which has small projections that do not exceed the length of the calyx lobes (Fig. 66D). Wurdack (1966) considered that this specimen might be a different variety because of its smaller flowers. For this reason, we include Vargas 10644 under M. vargasii with reservations. Distribution and phenology:— Meriania vargasii is endemic to southern Peru (Department of Cusco) and grows in montane forests at 1400–2800 m (Fig. 21). It has been collected in flower from March to June, and in fruit in March, May and June. Specimens examined:— PERU. Cusco: Prov. La Convención, Dist. Echarate, alturas de Papelpata, 2082 m, 12°45’06”S, 72°36’37”W, 21 May 2007 (fr.), G . Calatayud et al. 3979 (NY!); Dist. Huayopata, localidad Amaybamba, Qda. Quinsapuncuyoc, 1690 m, 12°35’S, 72°18’W, 18 May 2005 (fl.), G . Calatayud et al. 3181 (CUZ!, NY!), Balconpata, 2200 m, 12°51’01”S, 72°32’46”W, 16 Apr 2004 (fl.), G . Calatayud et al. 2255 (CUZ!, NY!), San Cristóbal, 2120 m, 12°58’51”S, 72°32’58”W, 06 May 2006 (fl.), H . van der Werff et al. 21425 (CUZ!, NY!); Dist. Maranura, Mesa pelada, 2536 m, 12°33’S, 72°22’W, 21 Apr 2005 (fl.), L . Valenzuela et al. 5600 (NY!), Mesapelada, 2400 m, 12°54’39”S, 72°37’25”W, 19 Apr 2004 (fl.), W . Galiano et al. 6156 (CUZ!, NY!); Dist. Ocobamba, Mesa pelada, 1451 m, 12°57’06”S, 72°38’29”W, 25 Mar 2004 (fl., fr.), L . Valenzuela et al. 3243 (CUZ!, NY!); Dist. Santa Ana, alrededores de Tunquimayo, 1800 m, 21 Apr 1952 (fl.), C . Vargas 10644 (CUZ!, US!), Tunquimayo, 2800 m, 13°03’S, 72°56’W, 15 Jun 2003 (fr.), E . Suclli & V. Chama 1015 (NY!); Dist. Vilcabamba, Paltaybamba, quebrada Fuentes Mayo, 1400 m, 13°01’38”S, 72°44’16”W, 08 Jun 2002 (fl.), L . Valenzuela et al. 152 (CUZ!, NY!).Published as part of Fernandez-Hilario, Robin, Goldenberg, Renato & Michelangeli, Fabián A., 2023, A synopsis of Meriania (Melastomataceae: Merianieae) in Peru, pp. 1-101 in Phytotaxa 602 (1) on pages 84-86, DOI: 10.11646/phytotaxa.602.1.1, http://zenodo.org/record/814198
Meriania drakei Wurdack, Mem.
<p> <b>8.</b> <i>Meriania drakei</i> (Cogn.) Wurdack, Mem. New York Bot. Gard. 16: 3 (1967).</p> <p> Basionym: <i>Axinaea drakei</i> Cogn. in A.DC. & C.DC., Monogr. Phan. 7: 447 (1891).</p> <p> Type: <b>ECUADOR:</b> Quebrada near Loja, 09 Nov 1881 (fl.), <i>Poortman 149</i> (lectotype, first step designated by Wurdack 1980, second step designated by Fernandez-Hilario <i>et al.</i> 2021: P! [barcode P00228665]; isolectotypes: BR!-fragment [barcode BR0000005628759], F!-fragment [accession no. 935562], P! [barcode P0228664]). (Figures 24–25).</p> <p> <b>Comments:—</b> <i>Meriania drakei</i> can be easily recognized by its externally puberulent petals (Fig. 24F), and it is also the only Peruvian species with a swollen adaxial projection on the apex of the petiole (Fig. 24D). Although Mendoza-Cifuentes (2021) mentions that this character is not constant in the Colombian populations, it is constant in the petioles of the Peruvian specimens examined. Other species such as <i>M. bicentenaria</i>, <i>M. franciscana</i>, <i>M. megaphylla</i> and <i>M. zunacensis</i> have an adaxial projection (scutum) on the insertion of the petiole with the leaf blade, but in <i>M. bicentenaria</i> and <i>M. franciscana</i> sometimes those can be obscured by trichomes. However, <i>M. drakei</i> is easily distinguishable from all of them by the indumentum on the petals (externally puberulent vs. glabrous). A detailed comparison of <i>M. drakei</i> with related species can be found in Fernandez-Hilario <i>et al.</i> (2021).</p> <p> <b>Distribution and phenology:—</b> <i>Meriania drakei</i> occurs from southern Colombia to northern Peru (Department of Amazonas in montane forests at 2010–2280 m) (Fig. 9). It has been collected in flower in November and December, and in fruit in February.</p> <p> <b>Specimens examined:—</b> <b>PERU. Amazonas:</b> Prov. Bagua, Dist. Imaza, Reserva Comunal Chayu Nain, rumbo hacia el campamento Yumi Awai, 2010 m, 05°26’54”S, 78°18’50”W, 08–10 Nov 2022 (fl.), <i>R. Fernandez-Hilario et al. 2386</i> (MOLF!). Prov. Utcubamba, Dist. Cajaruro, Buffer Zone of the Cordillera del Colán National Sanctuary, 2280 m, 05°38’32.22”S, 78°15’13.32”W, 19-22 Dec 2019 (fl.), <i>R. Fernandez-Hilario et al. 1775</i> (HOXA!, MOLF!, NY!, UPCB!, USM!). Prov. Bongará, Dist. Yambrasbamba, Lechuza pathway of the Abra Patricia Biological Station, 2120 m, 05°41’18.89”S, 77°48’23.68”W, 21 Feb 2020 (fr.), <i>R. Fernandez-Hilario et al. 1937</i> (HOXA!, MOLF!, UPCB!).</p>Published as part of <i>Fernandez-Hilario, Robin, Goldenberg, Renato & Michelangeli, Fabián A., 2023, A synopsis of Meriania (Melastomataceae: Merianieae) in Peru, pp. 1-101 in Phytotaxa 602 (1)</i> on pages 31-33, DOI: 10.11646/phytotaxa.602.1.1, <a href="http://zenodo.org/record/8141984">http://zenodo.org/record/8141984</a>
Meriania tomentosa (Cogn.) Wurdack from Colombia collected by Z. Restrepo #10470
File Name: TOLI-24063-VER-01-P15-86.jpg
CÓDIGO FOTO: TOLI-24063-VER-01-P15-86-
Fotografía: SI
Nº TOLI: TOLI-24063
PARCELA: VER-01
CÓDIGO: P15-86
Nº COLECTA: 10470
NUEVOS COLECTORES: Wilmar López Oviedo
COLECTORES: Z. Restrepo
Nº MUESTRAS MONTADAS: 1
Homologación: Homologado
Nueva fecha del evento : 17/01/2019.
Fecha del evento: 24/10/2014.
Proyecto : Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana
Hábitat: Bosque húmedo montano (bh-M)
Continente: SA
Pais: Colombia
Estado/Provincia: Quindío
Municipio: Calarcá
Localidad: Reserva Natural El Vergel
Elevación minima en metros: 2764
Elevación maxima en metros: 2964
Latitud: 4.454
Longitud original: -75.621
datum geodésico: WGS 84
Latitud decimal: 4.454
Longitud decimal: -75.621
Identificado por: Humberto Mendoza
Fecha de identificación: 18/01/2019.
Familia antigua: Melastomataceae
Especie antigua: Meriania aff. tomentosa (Cogn.) Wurdack
Nombre cientifico: Meriania tomentosa (Cogn.) Wurdack
Reino: Plantae
Filo: Magnoliophyta
Clase: Equisetopsida
Orden: Myrtales
Familia nueva: Melastomataceae
Género nuevo: Meriania
especie nueva: tomentosa
Autoría del nombre científico: (Cogn.) Wurdack
: Melastomataceae
genero herbario: Meriania
especie herbario: tomentosa
Especie de herbario para TNRS: Meriania tomentosa
Especie corregida herbario y desde TNRS: Meriania tomentosa
Familia corregida desde TNRS: Melastomataceae
: 3147</p
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