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Adiantum viscosum A. Cádiz-Véliz & A.E. Villarroel, sp. nov. (Fig. 2, 3) Diagnosis: — Adiantum viscosum differs from A. gertrudis and A. glanduliferum by the presence of capitate and glandular trichomes covering the entire aerial part of the plant, including pinnules, rachis, petioles and petiolules, which produce a sticky and aromatic resin. Type:— CHILE. Valparaíso Region: San Felipe de Aconcagua Province, Putaendo, Cordón del Tabaco, Quebrada de Granallas, 32°36’39.41” S; 70°46’44.72” W, 1330 m elevation, 10 October 2021, A . Cádiz-Véliz & B. Palma-Villalobos 801 (holotype: JBN!; isotypes: SGO!, CONC!). Description:— Terrestrial and saxicolous herb. Rhizomes short and creeping, 2–4 mm in diam. Rhizome scales lanceolate, emarginate, 1.5–2.0 mm long, brown with entire margins, not ciliate. Fronds 12–27 cm long. Petioles 1–1.5 mm diam., 4–13 cm long, covered with lanceolate scales 1.5–2.5 mm, brown, grouped at the base. Blades 2–pinnate, rarely 3–pinnate, 9–15 × 6–9 cm, deltoid in outline, approximately half the length of the frond. Rachises straight. Petiolules 1–5 mm long. Pinnules 8–15 × 8–25 mm, flabellate to reniform in outline, base cuneate-symmetrical or asymmetrical, alternate, terminal pinnae usually larger than underlying ones, margin of sterile pinnules crenulateserrate, margin of fertile pinnules folded towards the underside, forming a false indusium. Veins dichotomous, terminating between the crenulate margins. Trichomes on the aerial parts of the plants, (including pinnules, rachis, petioles and petiolules) dense, capitate, glandular, 0.4–0.6 mm, 3–4 cellular, yellowish, hyaline, exuding a sticky and aromatic resin. False indusia 5–15 per pinnule, rectangular or reniform, with a depressed and hyaline basal margin. Spores not observed. Etymology:— The specific epithet refers to the viscous resin produced by the glandular trichomes. Distribution and habitat:— Currently, the only known locality of the species is the one reported in this manuscript, and corresponds to a southwest-exposed slope in the Quebrada de Granallas (Fig. 1), where it occupies an area Quillaja saponaria Molina (1782: 354) and Lithraea caustica Hooker & Arnott (1833: 175) (Luebert & Pliscoff 2017). Adiantum viscosum grows accompanied by Tropaeolum azureum Colla in Bertero (1832: 147), Colliguaja odorifera Molina (1782: 354), Porlieria chilensis, and Kageneckia oblonga Ruiz & Pavón (1798b: 289). Phenology:— Adiantum viscosum initiates the formation of its fronds in mid-winter, after the first rains (June– July). The aerial part dies during the dry and warm summer (December–March). Conservation status:— Using IUCN criteria (2012), Adiantum viscosum is proposed as Critically Endangered (CR) B1+B2ab (i,ii,iii), because the extent of occurrence (EOO) is et al. 2012). In addition, the Cordón del Tabaco is threatened by mining projects, overgrazing, burning, drought, and unregulated tourism, which could affect the species (Madrid et al. 2018, Cádiz-Véliz & Aliaga-Reyes 2019). Adiantum viscosum is not present in any area of the Sistema Nacional de Áreas Silvestres Protegidas del Estado (SNASPE). Additional specimens examined: Adiantum gertrudis — CHILE. Región de Valparaíso, Provincia de Limache: cerro La Campana, 28 April 1968, C. Villagrán s.n. (SGO 86094); cerro La Campana, 28 October 1968, C. Villagrán s.n. (SGO 83853); cerro La Campana, 1200 m, 28 April 1968, C. Villagrán & A. Mesa s.n. (CONC 33060); cerro La Campana, 1350 m, 24 May 1936, A. Garaventa 3106 (CONC 51092); cerro La Campana, 1300 m, 17 January 1937, A. Garaventa 3250 (CONC 51091); cerro La Campana, 1500 m, 10 December 1938, A. Garaventa 6512 (CONC 51101); cerro La Campana, 1300 m, February 1958, P. Valenzuela 49316 (CONC 97032); cerro La Campana, 1500 m, December 1950, B. Collantes 21702 (CONC 97033); cerro Las Vizcachas, 1300 m, 24 January 1961, C. Behn 4326 (CONC 50160); Provincia de Valparaíso: Quebrada Verde, 2 October 1966, W. Sielfeld s.n (SGO 118182); Jardín Botánico Nacional, 110 m, 2 October 1976, A. Guajardo s.n. (CONC 150685); cuesta Balmaceda Fundo Los Perales, 300 m, 33º6’29.11’’S, 71º37’31’’O, 15 October 2015, S. Teillier & J. Macaya, 8485 (CONC 186661). Adiantum glanduliferum — CHILE. Región de Antofagasta, Provincia de Antofagasta: quebrada de Miguel Díaz, Punta Miguel Díaz, 400 m, 12 October 1941, E. Pisano & R. Bravo 450 (SGO 102164); quebrada del Rincón, Rinconada de Paposo, 250 m, 24º56’S, 70º29’O, 02 December 1989, O. Gálvez, A. Cornejo & M. Villarroel 48 (SGO 127410); Taltal, 20 m, 25º24’S, 70º29’O, 26 September 1940, S. Simpfendorfer s.n. (CONC 97133); Quebrada de San Miguel Rinconada de Paposo, 350 m, 24º58’S, 70º28’O, 4 December 1988, A. Hoffmann 302 (CONC 99049); Quebrada Matancilla, 500 m, 25º06’S, 70º27’O, 27 November 1997, M. Dillon & M. Villarroel 8121 (CONC 150013). Región de Atacama, Provincia de Huasco: Mina Oriente, camino a Carrizal Bajo, 12 October 1992, M. Muñoz 3053 (SGO 131464); Camino a Carrizal Bajo, km 44, 200 m, 28º09’S, 70º57’O, 26 October 1965, M. Ricardi, C. Marticorena & O. Matthei, 1527 (CONC 33988); Huasco, 10 m, 28º28’S, 71º13’O, 15 August 1966, G. Montero 7570 (CONC 63734). Región de Coquimbo, Provincia de Limarí: Fray Jorge, 7 October 1947, B. Sparre 2865 (SGO 102105); Zorrilla, 400 m, 30º50’S, 71º30’O, 5 January 1948, C. Jiles 530 (CONC 33978); Quebrada Toro, 330 m, 30º51’S, 71º18’O, 28 December 1950, C. Jiles 1924 (CONC 33987); Monte Redondo, 400 m, 31º03’S, 71º35’O, 1 October 1947, C. Jiles 332 (CONC 33990); Monte Redondo, 400 m, 31º03’S, 71º35’O, 17 November 1947, C. Jiles 492 (CONC 102113), Fray Jorge, 450 m, 30º40’S, 71º40’O, September 1958, J. Kumerow s.n. (CONC 39881), Provincia de Choapa: río Choapa, 750 m, 31º35’S, 71º32’O, February 1974, R. Torres s.n. (CONC 97134); quebrada El Pangue, 14 km al norte de los Vilos, 120 m, 31º48’S, 71º30’O, 16 October 1971, C. Marticorena, R. Rodríguez & E. Weldt 1390 (CONC 35767); 8 km al norte de Vilos, 30 m, 31º45’S, 71º31’O, 12 October 1963, C. Marticorena & O. Matthei 107 (CONC 33966). Región de Valparaíso, Provincia de Petorca: Chincolco, November 1942, M. Espinosa s.n. (SGO 81656); Zapallar, 11 October 1975, M. Valenzuela s.n. (SGO 135226); Zapallar, November 1980, E. Barrera s.n. (SGO 82908); Puente Guaquén, Carretera Panamericana, 30 m, 32º21’S, 71º27’O, 15 October 1971, C. Marticorena, R. Rodríguez & E. Weldt 1311 (CONC 35765); Pichicuy, 5,20 m, 32º20’S, 71º28’O, 1 November 1974, C. Marticorena, O. Matthei & R. Rodríguez 203 (CONC 43020); Petorca, 700 m, 32º15’S, 70º56’O, 16 September 1937, G. Montero 3156 (CONC 63733); Provincia de San Felipe: Santuario Serranía El Ciprés, 1260 m, 32º40’40’’ S, 70º48’39’’O, 24 August 2013, A. Madrid & J. Larraín 14 (CONC 186148); cerro de lo Vargas, 980 m, 32º40’S, 70º35’O, 17 February 1953, F. Torres s.n. (CONC 38402); Provincia de Valparaíso: Dunas de Concón, 32º56’ S, 71º32’O, 01 October 2002, S. Elórtegui s.n. (SGO 152627); Santuario de la Naturaleza Palmar El Salto, quebrada el Quiteño, 100 m, 33º03’S, 71º30’O, 01 October 2006, L. Flores & F. Aguirre s.n. (SGO 155647); Loncura, 32º46’S, 7132’O, November 1953, H. Gunckel 27.368 (CONC 96929); Quebrada Verde, 30 m, 33º02’S, 71º38’O, 24 August 1943, H. Schlegel 99 (CONC 39901); Cuesta Zapata, 700 m, 33º23’S, 71 º15’O, 27 November 1971, C. Elgueta s.n. (CONC 97045); Provincia de Marga-Marga: Limache, 130 m, 32º59’S, 71º15’O, September 1923, A. Garaventa 703 (CONC 102965); Provincia de San Antonio: Mirasol Algarrobo, 50 m, 33º20’S, 71º39’O, 21 October 1961, C. Aste 38.257 (CONC 96925); Algarrobo, 100 m, 33º21’S, 71º37’O, 2 November 1990, M. Baeza & P. Peñailillo s.n. (CONC 113367). Región Metropolitana, Provincia de Cordillera: Termas de Colina, 15 October 1943, J. Guzmán s.n. (SGO 081570); Provincia de Santiago: Quebrada de Peñalolén, 720 m, 33º28’S, 70º32’O, 10 December 1965, M. Mahu 2573 (CONC 37835); Quebrada Agua del Palo cerro Manquehue, 750 m, 33º22’S, 70º35’O, 10 October 1960, P. Valenzuela 13 (CONC 96924); Macul, 850 m, 33º30’S, 70º31’O, November 1954, A. Masena s.n. (CONC 96928); El Arrayán, 1000 m, 33º21’S,70ª28’O, 27 September 1952, H. Gunckel 26.608 (CONC 96953). Región de O’Higgins, Provincia del Cachapoal: Rancagua, 120 m, 32º22’S, 71º15’O, September 1926, C. Joseph s.n. (CONC 96932); Región del Maule, Provincia de Curicó: costa norte de Llico, 19 November 1969, C. Villagrán s.n. (SGO 85162); Querelema, Vichuquén, February 1923, E. Moore s.n. (SGO 81614); 8 km al norte de Reserva Nacional Laguna Torca, 20 m, 34º42’S, 72º02’O, 13 December 2000, L. Finot & M. Leppe 89 (CONC 150566); Provincia de Cauquenes: 10 m, 35º49’S, 72º35’O, January 1983, N. Toro s.n. (CONC 96948). Región del Ñuble, Provincia del Ñuble: Camino de Trehuaco a Mela, 35 m, 36º25’S, 72º41’O, 28 November 2000, M. Baeza, P. López & M. Parra 1954 (CONC 154386). Región del Bío-bío, Provincia del Biobío: Nacimiento, 70 m, 37º30’S, 72º40’O, E. Barros 517 (CONC 96943). Taxonomic relationships: —As mentioned above, Adiantum viscosum is morphologically similar to A. gertrudis and A. glanduliferum. However, A. poiretii Wikström f. bottini (Giudice & Nieto) Giudice (2016: 337), which inhabits the Andes of Mendoza Province (Argentina) also has glandular trichomes on the rachis, petiolules and the lower part of the pinnules (Giudice 1999, Giudice 2016). Table 1 shows the morphological differences between those four species., Published as part of Cádiz-Véliz, Arón, Palma-Villalobos, Bárbara, Villarroel, Alejandro E. & Muñoz-Schick, Mélica, 2023, Adiantum viscosum (Pteridaceae), a new species endemic to sclerophyllous forest of Central Chile, pp. 183-192 in Phytotaxa 599 (3) on pages 185-189, DOI: 10.11646/phytotaxa.599.3.5, http://zenodo.org/record/8012573, {"references":["Molina, J. I. (1782) Saggio sulla storia naturale del Chili. Bologna, Stamperia di S. Tommaso d´Aquino, 367 pp. https: // doi. org / 10.5962 / bhl. title. 62689","Hooker, W. J. & Arnott, G. A. W. (1833) Botanical Miscellany. Vol. 3. London, 390 pp.","Luebert, F. & Pliscoff, P. (2017) Sinopsis bioclimatica y vegetacional de Chile: segunda edicion. Editorial Universitaria, Santiago, Chile, 381 pp.","Bertero, C. G. (1832) Plantae rariores in regionibus chilensibus as Cl. M. D. Bertero nuper detectae, et a Colla ub lucm editae. Nuovo Giornale de' Letterati. Scienze. 24: 143 - 148. [Pisa]","Ruiz, H. & Pavon, J. A. (1798 b) Flora peruviana, et chilensis prodromus, sive descriptiones, et icones plantarum peruvianarum, et chilensium, secundum systema Linnaeanum digesta, vol. 1. Romae: Paleariniano. https: // doi. org / 10.5962 / bhl. title. 814","Luebert, F. & Pliscoff, P. (2012) Variabilidad climatica y bioclimas de la Region de Valparaiso, Chile. Investigaciones Geograficas (44): 41 - 56. https: // doi. org / 10.5354 / 0719 - 5370.2012.26408","Madrid, A., Larrain, J., Macaya, J. & Teillier, S. (2018) Contribucion al conocimiento de la flora del Santuario de la Naturaleza Serrania El Cipres, Region de Valparaiso, Chile. Gayana Botanica 75 (2): 589 - 624. http: // dx. doi. org / 10.4067 / S 0717 - 66432018000200589","Cadiz-Veliz, A. & Aliaga-Reyes, C. (2019) Nuevo registro para Avellanita bustillosii Phil. (Euphorbiaceae) en la Region de Valparaiso, Chile. Gayana Botanica 76 (2): 253 - 256. http: // dx. doi. org / 10.4067 / S 0717 - 66432019000200253","Giudice, G. E. (2016) Adiantum. In: Zuloaga, F. O. & Belgrano, M. J. (Eds.) Flora Vascular de la Republica Argentina, Vol. 2, Licofitas. Helechos. Gymnospermae, Flora Argentina 2. Editorial del Instituto Darwinion, Buenos Aires, pp. 330 - 340.","Giudice, G. E. (1999) Sinopsis de las especies argentinas del genero Adiantum (Pteridaceae, Pteridophyta). Darwiniana 37: 279 - 300. [https: // www. jstor. org / stable / 23223911]"]}

Identification key to Adiantum species in Chile, modified from Rodríguez (1995, 2015) and Sundue et al. (2010) 1. Pinnules glabrous................................................................................................................................................................................2 - Pinnules not glabrous.........................................................................................................................................................................5 2. Blades 1 pinnate.................................................................................................................................................................. A. pearcei - Blades 2–3 pinnate.............................................................................................................................................................................3 3. Veins sparse (≤4), spaced, conspicuous; rachises with septate trichomes and narrow scales up to 2 mm long; blades herbaceous............................................................................................................................................................................................... A. excisum - Veins numerous (>4), approximate, inconspicuous; rachises glabrous; blades coriaceous...............................................................4 4. Apical pinnules cuneate-flabellate; veins ending in the center of a tooth.............................................................. A. capillus-veneris - Apical pinnules subtrapezoidal or reniform; veins ending between two teeth................................................................... A. chilense 5. Blades with simple or glandular trichomes........................................................................................................................................6 - Blades with glomerular trichomes (mealy texture)............................................................................................................................8 6. Blades with simple, non-glandular trichomes, without sticky or aromatic resin...............................................................................7 - Blades with capitate and glandular trichomes, producing sticky and aromatic resin........................................................ A. viscosum 7. Blades with trichomes ≤ 1 mm long; pinnae subtrapezoidal to reniform................................................................... A. glanduliferum - Blades with trichomes 1–1.5 mm long; pinnae rhomboidal.............................................................................................. A. gertrudis 8. Pinnules covered with white glomerular trichomes.......................................................................................................... A. scabrum - Pinnules covered with yellow glomerular trichomes.........................................................................................................................9 9. Glomerular trichomes rounded........................................................................................................... A. sulphureum var. sulphureum - Glomerular trichomes elongated................................................................................................................. A. sulphureum var. majus, Published as part of Cádiz-Véliz, Arón, Palma-Villalobos, Bárbara, Villarroel, Alejandro E. & Muñoz-Schick, Mélica, 2023, Adiantum viscosum (Pteridaceae), a new species endemic to sclerophyllous forest of Central Chile, pp. 183-192 in Phytotaxa 599 (3) on pages 189-190, DOI: 10.11646/phytotaxa.599.3.5, http://zenodo.org/record/8012573, {"references":["Rodriguez, R. (1995) Flora de Chile, Vol. 1. Pteridophyta. Ediciones de la Universidad de Concepcion, Concepcion, Chile, pp. 119 - 309.","Sundue, M. A., Prado, J. & Smith, A. R. (2010) Adiantum camptorachis (Pteridaceae), a new species from South America with notes on the taxonomy of related species from the Southern Cone and Bolivia. American Fern Journal 100 (4): 195 - 206. http: // dx. doi. org / 10.1640 / 0002 - 8444 - 100.4.195"]}

Cádiz-Véliz, Arón, Palma-Villalobos, Bárbara, Villarroel, Alejandro E., Muñoz-Schick, Mélica (2023): Adiantum viscosum (Pteridaceae), a new species endemic to sclerophyllous forest of Central Chile. Phytotaxa 599 (3): 183-192, DOI: 10.11646/phytotaxa.599.3.5, URL: http://dx.doi.org/10.11646/phytotaxa.599.3.5

According to Escobar (2012), there are two kinds of floral appendages around the staminal tube or urn in Miersia: 1) the upper pair of appendages are of staminal origin and 2) the four lateral appendages, one pair on each side of the staminal tube, are of tepaliferous origin. Consequently, mentions to "tepaliferous appendages" in diagnoses, descriptions, identification key and figure captions of our recent article (García et al. 2022) should be changed to "floral appendages", to denote the mixed nature of those structures in most species of Miersia.

Ivania juncalensis Al-Shehbaz (2010: 345). (Fig. 1, 3) Type: — CHILE. Región de Valparaíso, Provincia de Los Andes, Valle del Río Juncal, 2500 m.a.s.l., 15 December 1976, Otto Zöllner 9165 (Holotype NA 5434). Description (Modified from Al-Shehbaz 2010): —Herbs, perennial, glabrous throughout. Caudex woody, densely covered with petiolar remains of previous years, several branches terminated in rosettes. Stems 8‒30 cm, erect, leafy. Basal leaves rosulate, not fleshy, more or less leathery; petiole 3.5‒9 cm; blade 2‒8 × 0.7‒3.5 (5) cm, oblong to lanceolate, pinnatifid to pinnatisect, base cuneate. Cauline leaves 1‒5 × 0.1‒1 cm, petiolate, linear-oblanceolate, entire to pinnatifid. Raceme elongated in fruit 5–12 cm long, branched, with cauline leaves up to the first flower of each branch; pedicels 1‒2 cm, divaricate-ascending. Sepals 2.5‒3 mm, ovate; petals 6‒7.5 × 2.5‒3 mm, white, spatulate, claw 3‒3.5 mm long; filaments 3‒3.5 mm long; anthers ca. 1 mm long, oblong; gynophore absent (~ 0.5 mm long in fruit); style 0.2‒0.5 mm long; stigma capitate, strongly 2‒lobed. Fruit siliqua, 2.5‒5 × 0.1‒0.2 cm, linear, slightly curved, terete, each valve with 2-3 longitudinal veins, replum terete, septum complete and veinless; seeds 2‒3 × 1 mm, uniseriate on each valve, numerous, pyramidal, acuminate, brown. Distribution and habitat: — Ivania juncalensis is endemic to the Andes of the Región de Valparaíso (Al-Shehbaz 2010, Rodríguez et al. 2018) and, until now, it is only known from the locality reported in this article. It is located in the private protected area Parque Andino Juncal, in the Río Juncal valley, Región de Valparaíso, Chile (Fig. 2). It is found between 2500 and 2900 m.a.s.l. in the “Mediterranean Andean dwarf scrub of Chuquiraga oppositifolia D. Don (1832: 392) and Nardophyllum lanatum (Meyen) Cabrera (1954: 63) ” vegetation type, which is found on high hillsides of the Andes between the provinces of Choapa and Colchagua (Luebert & Pliscoff 2017). However, I. juncalensis grows exclusively in rock crevices (Fig. 3), generally oriented towards the southwest, where it was observed along with Bowlesia tropaeolifolia Gillies & Hook. (1830: 325), Cystopteris apiiformis Gand (1913: 28), and Valeriana stricta Clos ([in Gay] 1848: 235). Based on field observations, we estimate its population size is less than 250 mature individuals. Studied material: — CHILE. Valparaíso: Los Andes Province, Juncal River Valley, Parque Andino Juncal, La Yesera sector, on a rocky slope with SW exposure, 32°54’14”S; 70°05’40”W, 2870 m.a.s.l., November 29th, 2021, A. Cádiz-Véliz & N. Marín 802 (JBN!, EIF!, VALPL!, SGO!, CONC!); February 14th, 2022, A. Cádiz-Véliz & B. PalmaVillalobos 961 (EIF). Ecology: —During the visits we did not observe pollinators, but we presume the species is pollinated by bees and/or flies due to the presence of nectaries and its floral morphology. After fruits dehisce, seeds are primarily gravity dispersed and helped by wind and water. It is likely that most seeds fall near the mother plant, which could partially explain its extremely restricted distribution. Phenology: —Flowers from early November to late December, and fruits from mid-December to mid-February. Conservation status: —The conservation status of I. juncalensis had not been assessed until now, although Warwick et al. (2011) mentioned it should be listed as “highly endangered”. Here we propose to list it as Critically Endangered (CR) B1+B2a (i,ii,iii) following the IUCN (2012) criteria, as its extent of occurrence (EOO) is et al. 2012). Some individuals showed signs of herbivory and we observed exotic lagomorphs in its habitat. Moreover, in the Andes of the Valparaíso Region there is goat and cattle farming, and multiple mining projects, such as the Nutrex mining project located less than 3 km away from the collection locality (Fig. 2). Taxonomic and phylogenetic considerations: The type species of Ivania was originally described by Johnston (1929) in Cardamine L. (1753: 654) and later transferred to Ivania (Schulz 1933). However, morphological differences to distinguish both genera have not been proposed. The genus Cardamine (Cardamineae tribe) is characterized by the presence of siliquae linear to subulate, latiseptate or rarely subterete with valves dehiscing elastically, and flattened replum, while Ivania (Thelypodieae) has siliquae linear and terete, with valves not dehiscing elastically, and terete replum (Appel & Al-Shehbaz 2003). Nevertheless, phylogenetic analyses using ITS clearly placed both Ivania species within the Thelypodieae tribe, along with other South American genera such as Chilocardamum O.E. Schulz (1924: 179), Pringlea W.Anderson ex Hook. f (1845: 238), and Polypsecadium O.E. Schulz (1924: 176), although the phylogenetic resolution within this tribe is very poor (Warwick et al. 2011). Even though the monophyly of Ivania was shown by Warwick et al. (2011), it is difficult to diagnose this genus considering several outstanding morphological differences between both species (Al-Shehbaz, 2010). For example, Ivania cremnophila has an evident gynophore of 2–4 mm long, while it is absent to only 0.5 mm long in I. juncalensis (absent according to Al-Shehbaz (2010)). Before the description of I. juncalensis, the presence of a gynophore longer than 2 mm was used in the generic key of Appel & Al-Shehbaz (2003) to separate Ivania from other similar genera; therefore, a clear morphological distinction of Ivania in relation to other genera in Brassicaceae is lacking. However, Ivania is characterized by entirely glabrous plants, while most species of related genera have simple and/or forked hairs. The presence of longitudinal veins on the fruit valves of Ivania juncalensis is a potential synapomorphy shared with other genera in Thelypodieae, such as Mostacillastrum and Stenodraba O.E. Schulz (1924: 186)., Published as part of Cádiz-Véliz, Arón, Román, Nicolás Marín, Urbina-Casanova, Rafael, Berguecio, Nicolás García, Palma-Villalobos, Bárbara & Sapaj-Aguilera, Guillermo, 2022, Rediscovery of Ivania juncalensis Al-Shehbaz (Thelypodieae; Brassicaceae), an endemic and threatened species from the Andes of Central Chile, pp. 276-282 in Phytotaxa 558 (3) on pages 277-280, DOI: 10.11646/phytotaxa.558.3.3, http://zenodo.org/record/7003051, {"references":["Rodriguez, R., Marticorena, C., Alarcon, D., Baeza, C., Cavieres, L., Finot, V. L., Fuentes, N., Kiessling, A., Mihoc, M., Pauchard, A., Ruiz, E., Sanchez, P. & Marticorena, A. (2018) Catalogo de las plantas vasculares de Chile. Gayana Botanica 75 (1): 1 - 430. https: // doi. org / 10.4067 / S 0717 - 66432018000100001","Luebert, F. & Pliscoff, P. (2017) Sinopsis bioclimatica y vegetacional de Chile: segunda edicion. Editorial Universitaria. Santiago, Chile, 381 pp.","Warwick, S. I., Sauder, C. A. & Al-Shehbaz, I. A. (2011) Systematic position of Ivania, Scoliaxon, and Phravenia (Brassicaceae). Taxon 60 (4): 1156 - 1164. https: // doi. org / 10.1002 / tax. 604017","Pliscoff, P., Arroyo, M. T. K. & Cavieres, L. (2012) Changes in the main vegetation types of Chile predicted under climate change based on a preliminary study: models, uncertainties and adapting research to a dynamic biodiversity World. Anales Instituto Patagonia (Chile) 40 (1): 81 - 86. https: // doi. org / 10.4067 / S 0718 - 686 X 2012000100010","Schulz, O. E. (1933) Uber verschiedene Cruciferen. Repertorium novarum specierum regni vegetabilis 33 (8 - 17): 183 - 191. https: // doi. org / 10.1002 / fedr. 19330330807","Schulz, O. E. (1924) Cruciferae-Sisymbrieae. In: Engler, A. (Ed.) Pflanzenreich IV. 105 (Heft 86). Verlag von Wilhelm Engelmann Leipzig 388 pp."]}

Key to Brassicaceae genera with native species in the Valparaiso Region, Chile (based on Boelcke & Martínez-Laborde 1994; Appel & Al-Shehbaz 2003; Al-Shehbaz 2012) 1. Petals pinnatifid............................................................................................................................................................. Schizopetalon 1. Petals entire or emarginate.................................................................................................................................................................2 2. Petals white.........................................................................................................................................................................................3 3. Fruit a silique, at least three times larger than wide...........................................................................................................................4 4. Seeds biseriate......................................................................................................................................................................... Rorippa 4. Seeds uniseriate..................................................................................................................................................................................5 5. Basal and cauline leaves pinnatisect or pinnately compound. Fruit valves not veined, dehiscing elastically and coiled; replum flattened.............................................................................................................................................................................. Cardamine 5. Basal leaves pinnatifid, lobed or entire, cauline leaves lobed to entire. Fruit valves obscurely veined or only with a distinct midvein, not dehiscing elastically, flat; replum terete........................................................................................................................6 6. Plants entirely glabrous. Petals> 6 mm long............................................................................................................................ Ivania 6. Plants usually with simple and/or forked hairs, rarely glabrous. Petals Mostacillastrum 7. Plants shorter than 10 cm high. Flowering stems scapigerous, at most with 1–2 leaves. Silique up to 2.5(–3.0) cm long at maturity.............................................................................................................................................................................. Stenodraba 3. Fruit a silicle, less than three times longer than wide.........................................................................................................................8 8. Fruit with 1 or 2 seeds........................................................................................................................................................................9 9. Fruit valves with 2, 3, or 5 longitudinal wings, rarely wingless. Septum lacking........................................................... Menonvillea 9. Fruit valves wingless or with 1 wing. Septum complete....................................................................................................... Lepidium 8. Fruit with more than 2 seeds........................................................................................................................................................... 10 10. Cauline leaves auriculate. Fruit compressed dorsiventrally, ± winged. Plant glabrous......................................................... Noccaea 10. Cauline leaves, if present, never auriculate. Fruit compressed laterally, wingless. Plant pubescent, at least some trichomes stellate................................................................................................................................................................................................... Draba 2. Petals yellow..................................................................................................................................................................... Descurainia, Published as part of Cádiz-Véliz, Arón, Román, Nicolás Marín, Urbina-Casanova, Rafael, Berguecio, Nicolás García, Palma-Villalobos, Bárbara & Sapaj-Aguilera, Guillermo, 2022, Rediscovery of Ivania juncalensis Al-Shehbaz (Thelypodieae; Brassicaceae), an endemic and threatened species from the Andes of Central Chile, pp. 276-282 in Phytotaxa 558 (3) on pages 280-281, DOI: 10.11646/phytotaxa.558.3.3, http://zenodo.org/record/7003051

Cádiz-Véliz, Arón (2021): Miersia putaendensis sp. nov. (Gilliesieae, Amaryllidaceae), a new species endemic to Central Chile. Phytotaxa 502 (3): 230-236, DOI: 10.11646/phytotaxa.502.3.2, URL: http://dx.doi.org/10.11646/phytotaxa.502.3.2

Two new populations of Avellanita bustillosii Phil., an endemic endangered (EN) shrub of Chile central, is documented near Putaendo, Valparaíso. This new record constitutes the fifth and sixth population of the species, which extends the northern boundary of distribution and a establishes a new altitudinal boundary.

[This corrects the article DOI: 10.3897/phytokeys.211.87842.]., (Nicolás García, Claudia Cuevas, Joaquín E. Sepúlveda, Arón Cádiz-Véliz, María José Román.)