Baccharis napaea G.Heiden

Heiden, Gustavo & Pirani, José Rubens, 2012, Baccharis napaea (Asteraceae, Astereae): a new species of subgen. Tarchonanthoides sect. Coridifoliae from the subtropical highlands of southern Brazil, Phytotaxa 66 (1), pp. 49-54: 50-53

publication ID

http://doi.org/ 10.11646/phytotaxa.49.1.3

persistent identifier

http://treatment.plazi.org/id/D757560B-FF8F-FFE5-E2C3-52C1FD86F832

treatment provided by

Felipe

scientific name

Baccharis napaea G.Heiden
status

sp. nov.

Baccharis napaea G.Heiden   , sp. nov. ( Fig. 1)

Baccharis napaea G.Heiden   is characterized by its tomentose and lanate indumentum of developed shoots and leaves, differing from B. erigeroides DC.   and B. coridifolia DC.   which are characterized by glabrescent developed shoots and glabrescent leaves, and from B. scabrifolia G.Heiden   that is characterized by shoots and leaves with villous and scabrous indumentum.

Type:— BRAZIL. Paraná: Palmas, Horizonte, divisa PR / SC, Campos de Água Doce e Palmas , BR 280, próximo às turbinas da Central de Energia Eólica de Palmas , 1303 m, fl., ♀, 8 February 2011, G. Heiden, J. M. da Silva & J. M. Vaz 1581 (holotype SPF!; isotypes FLOR!, ICN!, F!, JE!, K!, LP!, MBM!, MVFA!, MO!, PACA!, RB!, SP!,   US!, and Herbário da Embrapa Clima Temperado , Pelotas, RS, Brasil!)   .

Subshrubs 1–1.5 m tall, erect; sterile lateral shoots prostrate, fertile shoots ascending, terminating in a capitulescence, greenish to greyish; indumentum tomentose, hairs filiform. Leaves 1–4.4 cm long, 0.14–0.28 cm wide, greenish to greyish, sessile; leaf blade chartaceous, linear, plane, apex acute, base attenuate, margins entire, ciliate; leaves 1-nerved, midrib flat on adaxial surface and slightly prominent on abaxial surface, both surfaces with a lanate indumentum (puberulous in very old leaves), filiform hairs and biseriate glandular hairs, tufted indumentum absent. Capitulescences paniculate, terminal; panicles conical to ellipsoid, 16–60 cm long, 6–18 cm wide. Capitula pedunculate; peduncles 2.2–5.3 mm long. Male capitula 2.2–3 mm long; florets 7–12; involucre 1.7–2.8 mm long, 2.6–3 mm wide, cup-shaped; phyllaries in 3 series, greenish, outer and median phyllaries ovate, innermost ones linear-lanceolate, margin broadly scarious, short-dentate, apex obtuse to acute; clinanthium (receptacle) convex, glabrous or with scattered biseriate glandular hairs and uniseriate hairs; corolla 1–2 mm long, tube 0.4–0.9 mm long, throat 0.1–0.3 mm, lobes 0.5–0.7 mm long, biseriate hairs on tube and throat; anthers including apical appendages 0.8–1 mm long; style 0.9–1 mm long, apex nearly fully cleft into broadly lanceolate branches with sweeping hairs of equal size; ovary abortive, puberulous with twin and biseriate glandular hairs; pappus uniseriate, 1.1–2 mm long, bristles 18–24, twisted, apically not broadened, with short-protruding, erecto-patent terminal cell apices. Female capitula 4.5–8 mm long; florets 5–10; involucre 4.1–4.8 mm long, 2.2–3.5 mm wide, cylindrical to campanulate, narrowed distally; phyllaries in 4–5 series, greenish, outer and median phyllaries ovate, innermost ones oblanceolate, margins scarious, short dentate, apex obtuse; clinanthium (receptacle) convex to conical, with scattered biseriate glandular hairs; corolla 2–3.1 mm long, filiform, with 5 papillose teeth; style 3.6–4 mm long, branches 0.4–0.8 mm long; cypselae 1.9–2.4 mm long, 0.7–1 mm wide, stramineous to light brown, covered with biseriate glandular hairs and twin hairs, cylindrical, slightly narrowed at base, 5–6 longitudinal ribs; pappus multiseriate, 2.6–4.3 mm long at cypsela maturity, persistent; bristles 80–140, connate basally, not broadened apically.

Distribution & habitat:— Baccharis napaea   occurs in the highlands of the south Brazilian plateau (Planalto Sul-Brasileiro, also known as Planalto Meridional), in elevations between 750 and 1300 m a.s.l., in the states of Paraná, Santa Catarina, and Rio Grande do Sul, in southernmost Brazil ( Fig. 2). It forms sparse populations, mainly across open grasslands within the subtropical highland grassland biome and along the edges or in open glades of Araucaria angustifolia (Bertol.) Kuntze   forest thickets, in the contact zone with the subtropical mixed forest biome ( Iganci et al. 2011). These environments occur in the transitional zone of high elevation grasslands and ombrophilous mixed forests of the Atlantic Rainforest Domain.

Phenology:— Baccharis napaea   flowers from February to March and specimens setting fruits were collected from April to June.

Conservation status: —Despite many efforts during the years of 2010 and 2011 looking for populations of B. napaea   in most of the known localities of occurrence of this species in southern Brazil, none of them were found except for a new record at the border of the municipalities of Água Doce (Santa Catarina) and Palmas (Paraná). The new species is well represented in herbaria; however, only three of these records were registered in the last 10 years (considering the authors’ records to the neighboring places of Paraná and Santa Catarina Border as one record). Since a wider former distribution of the species seems likely, we suspect that its area has been reduced in recent years due to the conversion of native grasslands into extensive fields of soybean, corn, and wheat, as well as by the great increase of pine plantations, and the invasion of pine seedlings into the native environments across the southern Brazilian highland grasslands in the last years. Because of the continuing decline of the area of the native grasslands, the loss of habitat quality and the effects of Pinus   invasion of the native vegetation the new species is assessed as Vulnerable: VU A2ce ( IUCN 2011).

Etymology: —The specific epithet (a noun in singular in apposition) refers to the Napaeae, the nymphs of valleys in Greek mythology, and the homonymous floristic province of Martius, referring to the alternate and intermittent distribution of grasslands and forests in this region.

Additional specimens examined (paratypes): — BRAZIL. Paraná: Curitiba, fl., ♂, 25 February 1907, P   . Dusén 3862 ( R, US); fl. & fr., ♂ & fl. ♂, 16 March 1909, P   . Dusén 7905 ( NY); fl., ♀, 24 February 1912, P   . Dusén 13867 ( E, SI); fl., ♀ & ♂, P   . Dusén 13867 ( LIL, MO); 900 m, fl., ♀, 12 March 1914, P   . Dusén 14593 ( MO, NY, US); Pinheirinho , 950 m, fl., ♂, 21 March 1962, G   . Hatschbach 8906 ( MBM, RB). Palmas , Horizonte, divisa PR / SC   , Campos de Água Doce e Palmas , BR 280   , próximo às turbinas da Central de Energia Eólica de Palmas , 51.672°W, 26.565°S, 1303 m, fl., ♂, 8 February 2011, G GoogleMaps   . Heiden, J. M   . da Silva & J. M   . Vaz 1580 ( ICN, JE, K, LP, MBM, RB, SPF). Piraquara, Pinhais , 907 m, fl., ♂, 18 February 1959, G   . Hatschbach 5502 ( HBR, LIL, MBM); fl., ♂, G   . Hatschbach 5503 ( LIL, MBM). Rio Negro, Campo do Tenente , fl. & fr., ♀, 1 April 1951, G   . Hatschbach 2176 ( MBM, SI); fr., ♀, 29 June 1960, G   . Hatschbach 7044 ( MBM). Rio Grande do Sul: Bom Jesus, rodovia Bom Jesus-São Joaquim , rio Pelotas , fl. & fr., ♀, 11 March 2005, G   . Hatschbach, E   . Barbosa & E. F   . Costa 79047 ( CTES, MBM). Vacaria, descida para o vale do rio Pelotas , fl., ♂, 11 January 1978, J   . Mattos 18319 ( HAS). Santa Catarina : Água Doce, Horizonte, divisa PR / SC   , Campos de Água Doce e Palmas , BR 280   , próximo às turbinas da Usina de Energia Eólica de Água Doce , 51.616°W, 26.589°S, 1316 m, bud, 11 January 2011, G GoogleMaps   . Heiden & J. R. V   . Iganci 1486 ( FLOR, ICN, LP, MBM, RB, SPF). Capão Alto, Fazenda Pai Querê , 50.618°W, 28.354°S, fr., ♀, 28 June 2009, R GoogleMaps   . Trevisan s.n. ( ICN 164765 View Materials ). Curitibanos, fl., ♂, March 1877, F   . Müller 68 ( R); Monte Alegre , fl., ♂, 25 February 1960, J   . Mattos 7653 ( HAS). Mafra , 750 km, bud, 26 January 1953, R   . Reitz 5283 ( HBR); 4 km northwest of Mafra on the road to Barracas (20 km), 800–850 m, fl., ♀, 13 March 1957, L. B   . Smith & R. M   . Klein 12082 ( HBR, NY, R, RB, US); fl., ♂, 13 March 1957, L. B   . Smith & R. M   . Klein 12083 ( HBR, NY, R, RB). Três Barras , fl., ♂, 26 February 1948, A   . Mattos & L   . Labouriau s.n. ( NY 782036 View Materials , RB 63243)   .

Baccharis napaea   is placed in subgenus Tarchonanthoides   because of the following combination of features: a conspicuous indumentum of filiform hairs and the lack of tufted indumentum, appearing as small resinous dots, typical of most Baccharis species   of other subgenera; the cup-shaped involucre of male capitula, contrasting with the cylindrical to campanulate involucre of the female capitula; apically not broadened pappus bristles of male florets; and the corollas of female florets with five papillose teeth. The new species is also assigned to the section Coridifoliae Giuliano (2011)   because of its sessile and 1-nerved leaves and the multiseriate and persistent pappus of female flowers, accrescent in cypsela maturity.

Most of the specimens of B. napaea   found in herbaria were determined as B. puberula Candolle (1836: 401)   or B. erigeroides DC. var. dusenii Heering (1910: 23)   ; both names are synonyms of the sympatric B. erigeroides Candolle (1836: 418)   , which is endemic to Brazil and occurs north to central Goiás state and south to northeastern Rio Grande do Sul state ( Heiden & Schneider 2012) in tropical savannahs (cerrado) and subtropical highland grasslands (campos de cima da serra). Baccharis napaea   can be distinguished from B. erigeroides   by its height (1–1.5 m vs. 0.3–0.7 m tall); the tomentose and lanate indumentum of shoots and leaves (vs. caducous filiform hairs found in leaves of young shoots that later become glabrescent); linear leaf blades (vs. narrow elliptic to narrow oblanceolate leaf blades) that are mostly smaller (1.1–4.4 × 0.14–0.28 cm vs. 4–5 × 0.3–0.7 cm), shorter peduncles (2.2–5.3 mm vs. 6–31 mm long), smaller male capitula (2.2–3 × 2.6–3 mm vs. 3–5 × 4.5–6.7 mm) with fewer florets (7–12 vs. 12–20), and fewer-flowered female capitula (5–10 vs. 12–22), with female florets with shorter pappus bristles (2.6–4 vs. 5.6–6.9 mm long).

Due to the similar habit, sessile linear 1-nerved leaves and broad paniculate capitulescences, B. napaea   superficially resembles the widespread and sympatric B. coridifolia Candolle (1836: 422)   , which occurs in grasslands, pastures and disturbed areas from lowlands to highlands across central Argentina, north to central Bolivia and south-eastern Brazil ( Müller 2006, Heiden & Schneider 2012). Despite this similarity, B. napaea   can be differentiated by the persistent tomentose and lanate indumentum of filiform hairs present in the developed shoots and leaves respectively (vs. caducous filiform hairs found on leaves of very young shoots that later become glabrescent), fewer-flowered male capitula (7–12 vs. 15–30), shorter corolla of female florets (2–3.1 mm vs. 3.2–4.5 mm long), and shorter pappus of mature cypselae (2.6–4 vs. 5.2–7.2 mm long). Baccharis scabrifolia Heiden (2008: 6)   , an endemic highland species of the south Brazilian plateau (Santa Catarina and Rio Grande do Sul) where it is restricted to peat bogs and swampy grasslands, is another sympatric species similar to B. napaea   . Both species can be separated by the tomentose and lanate indumentum of shoots and leaves of B. napaea   (vs. villous and scabrous indumentum of shoots and leaves of B. scabrifolia   ); not revolute, ciliate leaf margins and attenuate leaf bases (vs. revolute, not ciliate leaf margins and obtuse to subcordate leaf bases); fewer-flowered male capitula (7–12 vs. 12–16); and longer female capitula (4.5–8 vs. 2.5–3 mm long), female florets corollas (2–3.1 vs. 1.3–1.5 mm long), cypselae (1.9–2.4 mm vs. 1–1.2 mm long) and pappus (2.6–4 mm vs. 1.8–2.2 mm long).

With respect to its morphology, B. napaea   seems to be related to the allopatric Bolivian B. bicolor ( Müller 2006: 276) G. Heiden   (in Heiden & Pirani 2012: 45), from which it can be distinguished by its paniculate capitulescences (vs. partial capitulescences mostly racemose), few-flowered male capitula (7–12 vs. 18–30), shorter corolla of female florets (2–3.1 mm vs. 3.7–4.5 mm long), and shorter pappus of mature cypselae (2.6–4.3 vs. 5.3–6.5 mm long).

SC

Salem College

G

Conservatoire et Jardin botaniques de la Ville de Genève

J

University of the Witwatersrand

M

Botanische Staatssammlung München

SPF

Universidade de São Paulo

FLOR

Universidade Federal de Santa Catarina

ICN

Instituto de Ciencias Naturales, Museo de Historia Natural

F

Field Museum of Natural History, Botany Department

JE

Friedrich-Schiller-Universität Jena

K

Royal Botanic Gardens

LP

Laboratory of Palaeontology

MBM

San Jose State University, Museum of Birds and Mammals

MVFA

Universidad de la República

MO

Missouri Botanical Garden

PACA

Instituto Anchietano de Pesquisas/UNISINOS

RB

Jardim Botânico do Rio de Janeiro

SP

Instituto de Botânica

P

Museum National d' Histoire Naturelle, Paris (MNHN) - Vascular Plants

R

Departamento de Geologia, Universidad de Chile

NY

William and Lynda Steere Herbarium of the New York Botanical Garden

E

Royal Botanic Garden Edinburgh

SI

Museo Botánico (SI)

LIL

Fundación Miguel Lillo

PR

National Museum in Prague

HBR

Universidade Federal de Santa Catarina

CTES

Instituto de Botánica del Nordeste

HAS

Fundação Zoobotânica do Rio Grande do Sul

V

Royal British Columbia Museum - Herbarium

L

Nationaal Herbarium Nederland, Leiden University branch

B

Botanischer Garten und Botanisches Museum Berlin-Dahlem, Zentraleinrichtung der Freien Universitaet

A

Harvard University - Arnold Arboretum