Baccharis nebularis G.Heiden, 2014

Heiden, Gustavo & Pirani, José Rubens, 2014, Baccharis nebularis (Asteraceae, Astereae): a new species of B. subgen. Tarchonanthoides sect. Curitybenses from the mountains of Southern Brazil, Phytotaxa 177 (2), pp. 125-130 : 126-129

publication ID

https://doi.org/ 10.11646/phytotaxa.177.2.4

persistent identifier

https://treatment.plazi.org/id/039F8787-FFF1-D866-FF7A-FF051D74F929

treatment provided by

Felipe

scientific name

Baccharis nebularis G.Heiden
status

sp. nov.

Baccharis nebularis G.Heiden View in CoL , sp. nov. ( Figs. 1 View FIGURE 1 , 2 View FIGURE 2 )

Baccharis nebularis G.Heiden differs from B. chionolaenoides Falkenb. & Deble by pappus of male florets not twisted and broadened in the apex and by cypsela densely covered by twin trichomes; from B. curitybensis Heering ex Malme it is distinguished by leaves crowded at the apex of the branches and peduncles with a tomentose indumentum.

Type:— BRASIL. Paraná: Guaratuba, Serra de Araçatuba, Morro dos Perdidos , cume, 25° 53’ 21” S, 48° 57’ 28” W, 1411 m, 17 December 2010, ♀, G GoogleMaps . Heiden , J. R. V . Iganci , J. M . da Silva & J. M . Vaz 1449 (holotype SPF!; isotypes FLOR!, K!, MBM!, RB!, GoogleMaps US!).

Shrubs 0.5–2 m tall, erect; fertile shoots ascending, terminating in a capitulescence, proliferating. Stems brown, fissured, ochraceous or whitish in younger shoots; indumentum tomentose, trichomes filiform, flagelliform and biseriate glandular. Leaves 1.2–5 cm long, 0.7–2 cm wide, petioles 2–18 mm long, evenly distributed along the branches; leaf blade discoloured, adaxial surface green, abaxial surface white to ochraceous, chartaceous, obovate to elliptic, apex acute to obtuse, sometimes mucronulate, base acute, margin entire or with 1–3 pairs of teeth; leaves basally 3- nerved, acrodromous imperfect, with a secondary semicraspedodromous reticulum, adaxial surface with a caducous lanose indumentum, abaxial surface with a persistent felted indumentum, both surfaces with filiform, flagelliform and biseriate glandular trichomes. Capitulescences corymbose, terminal; corymbs lax, 3–6.5 cm long, 3.3–6.8 cm wide. Capitula pedunculate; peduncles 0.7–2.5 cm long, ochraceous, tomentose. Male capitula 4.7–6 mm long; florets 34–45; involucre 4–5 mm long, 7–9.6 mm wide, cup-shaped; phyllaries in 3–4 series, outer phyllaries and median phyllaries ovate, innermost phyllaries linear-lanceolate, margin entire, apex rounded; clinanthium plane, nearly glabrous, with scarce biseriate trichomes; corolla 3–3.6 mm long, tube 1.6–1.9 mm long, throat 0.7–0.9 mm, lobes 0.7–0.8 mm long, biseriate hairs on the lobes; anthers including apical appendages 2.3–2.7 mm long; style 2.3–2.9 mm long, branches free, lanceolate; ovary abortive, 0.3–0.5 mm long, 0.1–0.3 mm wide, covered by biseriate and twin trichomes; pappus uniseriate, 3.3–3.7 mm long, bristles 18–22, not twisted, apically broadened, with short-protruding, adpressed cell apices. Female capitula 6.7–8.5 mm long; florets 26–44; involucre 4.2–5.5 mm long, 7.3–9.9 mm wide, campanulate; phyllaries in 4–5 series, outer phyllaries elliptic, median ovate, innermost phyllaries oblanceolate-linear, margin entire, apex rounded; clinanthium plane, nearly glabrous, with scarce flagelliform trichomes; corolla 2.8–3 mm long, filiform, with 5 teeth; style 3.9–4.2 mm long, branches 0.3–0.5 mm long; cypselae 1.2–1.4 mm long, 0.4–0.8 mm wide, brown, evenly covered by twin trichomes, obconical, narrowed at base, 8–10 longitudinal ribs; pappus multiseriate, 2.9–3.2 mm long, deciduous; bristles 32–48, connate basally, slightly broadened apically, not elongated at cypsela maturity. Chromosome number unknown.

Etymology: —The specific epithet refers to the habitat in cloud forest thickets amidst high altitude grasslands.

Distribution and habitat: — Baccharis nebularis occurs in southern Brazil (Paraná and Santa Catarina) and is restricted to the summits of the peaks of the southernmost range of Serra do Mar, at elevations between 1400 and 1700 m a.s.l. ( Fig. 3 View FIGURE 3 ). It grows in patches of high altitude tropical grasslands mixed with cloud forest thickets ( Fig. 2 View FIGURE 2 ), forming sparse populations, in the buffer zone between the ombrophilous dense forest and the high altitude tropical grasslands of the Atlantic province.

Phenology: —Fertile specimens have been recorded from August to late December with a flowering peak in October and November.

Conservation status: —The new species is known from five massifs (Serra de Araçatuba, Serra de Capivari, Serra da Graciosa, Serra do Ibitiraquire or Serra dos Órgãos, and Serra do Quiriri— Fig. 3 View FIGURE 3 ), represented in herbaria by 24 collections made between 1960 and 2010. Only five of these collections, all from Serra do Araçatuba, were made in the last 10 years. The high altitude tropical grasslands and cloud forest environments in the southern range of Serra do Mar have different levels of accessibility and are partially covered by preserves of various levels, but several of its mountain peaks are private owned. The environment of the new species is naturally fragmented, related to the sky island distribution of its habitats. Some of these areas are remote and inaccessible, whereas others are under anthropogenic pressure such as cattle grazing, tourism, accidental fires, forestry and introduction of exotic species. Disturbances of the natural environment occur because some peaks can be reached by car for installation and maintenance of antennas and other telecommunication facilities in the summits. During the collection of the type specimens in Serra do Araçatuba it was observed that B. nebularis is a rare species with sparse populations and discontinuous distribution, but due to the lack of more precise information the data available was found to be insufficient to place the taxon into a category of threat and the new species is considered Data Deficient: DD ( IUCN 2013).

Etnobotany & vernacular names: —Unknown.

Specimens examined: — BRAZIL. Paraná: Campina Grande do Sul, Serra do Capivari , 23 October 1997, ♂, C. V . Roderjan & A. P . Tramujas 1510 ( MBM, UPCB); Capivari Grande , 23 October 2001, ♂, E . Barbosa, O. S . Ribas & E. F . Costa 670 ( B, MBM); Serra do Ibitiraquire (Serra dos Órgãos), 2 November 2001, ♂, A. Y . Mocochinski & M . Scheer 40 ( UPCB); Morro Camapuã , 9 September 1999, ♂, E . Barbosa, J. M . Silva & L. A . Ferreira 390 ( C, CTES, ESA, G, INPA, MBM); Morro Tucum , 19 November 1999, ♂, J . Cordeiro, J. M . Cruz & L. A . Ferreira 1643 ( B, CESJ, G, MBM, UFP); Pico Caratuva , 2 August 1967, 1950 m, ♂, G . Hatschbach 16829 ( MBM); 5 October 1967, G . Hatschbach 17322 ( CTES, K, MBM, MO, UPCB); ♂, 15 November 1967, G . Hatschbach 17845 ( HBR, MBM, UPCB). Guaratuba , Serra de Araçatuba , 9 November 1983, ♂, R . Kummrow 2391 ( GB, HBG, MBM, NY, UB, UPCB); 23 November 1996, ♂, E. P . Santos, H. M . Fernandes & C. M. S . Coimbra 297 ( MBM, UPCB); 1 December 1998, ♂, J. M . Silva, E . Barbosa & J. M . Cruz 2661 ( C, FLOR, G, HBG, HUEFS, K, MBM, NY, SPF); 25 February 2000, ♂, J. M . Silva, E . Barbosa & J . Cordeiro 3262 ( CESJ, ESA, HUEFS, MBM); 30 October 2003, ♂, J. M . Silva, E . Lucas, F. F . Mazine & C. M . Sakuragui 3809 ( CORD, MBM, NY, SP); Morro dos Perdidos , cume, 25° 53’ 21” S, 48° 57’ 28” W, 1411 m, 17 December 2010, ♂, G GoogleMaps . Heiden, J. R. V . Iganci, J. M . da Silva & J. M . Vaz 1450 ( MBM, RB, SPF, US); 9 November 1994, ♀, C. B . Poliquesi & J. M . Cruz 208 ( BHCB, HAS, MBM, UB); 9 September 2006, bud, G. O . Romão & A. P. T . Dantas 1676 ( BHCB, ESA, UEC); 29 October 2006, ♂, G. O . Romão, C . D. Rodrigues & A. P . Dantas 1496 ( BHCB, ESA, SPF, UEC); 23 November 1996, ♂, E. P . Santos, H. M . Fernandes & C. M. S . Coimbra 297 ( NY, UPCB). Quatro Barras, Serra da Graciosa , Morro Mãe Catira , 8 October 1985, ♀, R . Kummrow & J. M . Silva 2626 ( C, CORD, FLOR, GB, MBM, US); 31 October 1989, ♂, J. M . Silva & C. B . Poliquesi 655 ( MBM, SP). Santa Catarina: Campo Alegre, Serra do Quiriri , 19 November 1992, J . Cordeiro & C. B . Poliquesi 953 ( C, HUEFS, MBM, MO); 28 December 1999, ♀, J . Cordeiro, J. M . Silva, E . Barbosa & O. S . Ribas 1747 ( CTES, MBM). Garuva, Monte Crista , 6 October 1960, R . Reitz & R. M . Klein 10034 ( HBR, RB) GoogleMaps .

Baccharis nebularis is placed in B. subgen. Tarchonanthoides based on the following combination of features: conspicuous indumentum of filiform hairs and lack of tufted indumentum; cup-shaped involucres of male capitula, contrasting to cylindrical to campanulate involucres of female capitula, and corollas of female florets with five papillose teeth. The new species is assigned to B. sect. Curitybenses due to female flowers with deciduous pappus and ca. 10- ribbed cypselae covered by twin trichomes.

Both in habit and habitat, B. nebularis resembles the allopatric B. chionolaenoides : they are densely branched shrubs with leaves crowded at the apex of branches, growing in moist places in the transition zone of cloud forest thickets to open areas. However, B. chionolaenoides is endemic to the cliffs of Morro da Igreja further south in Santa Catarina, and the new species is more similar to the parapatric B. curitybensis , distributed in high altitude open and dry grasslands from Serra da Mantiqueira range in southeastern Minas Gerais and São Paulo south to the highlands of Aparados da Serra in Rio Grande do Sul. Baccharis curitybensis and B. nebularis have a small area of contact in the Serra do Quiriri massif, at the boundary between Paraná and Santa Catarina. In that area, open and dry high altitude grasslands co-exist with thickets of cloud forest and moist grasslands and both species are recorded there, although growing in distinct habitats. The studied specimens of B. nebularis were previously determined in herbaria as B. curitybensis . The two species have in common similar 3-nerved, entire or dentate leaves, corymbose capitulescences, cup-shaped male and campanulate female capitula, apically broadenend pappi of male florets, and cypselae densely covered by twin trichomes. A key for differentiating the three species of B. sect. Curitybenses is provided below.

G

Conservatoire et Jardin botaniques de la Ville de Genève

J

University of the Witwatersrand

R

Departamento de Geologia, Universidad de Chile

V

Royal British Columbia Museum - Herbarium

M

Botanische Staatssammlung München

SPF

Universidade de São Paulo

FLOR

Universidade Federal de Santa Catarina

K

Royal Botanic Gardens

MBM

San Jose State University, Museum of Birds and Mammals

RB

Jardim Botânico do Rio de Janeiro

C

University of Copenhagen

A

Harvard University - Arnold Arboretum

P

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

UPCB

Universidade Federal do Paraná

E

Royal Botanic Garden Edinburgh

O

Botanical Museum - University of Oslo

S

Department of Botany, Swedish Museum of Natural History

F

Field Museum of Natural History, Botany Department

B

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

Y

Yale University

L

Nationaal Herbarium Nederland, Leiden University branch

CTES

Instituto de Botánica del Nordeste

ESA

Universidade de São Paulo

INPA

Instituto Nacional de Pesquisas da Amazonia

CESJ

Universidade Federal de Juiz de Fora

UFP

Universidade Federal de Pernambuco

MO

Missouri Botanical Garden

HBR

Universidade Federal de Santa Catarina

GB

University of Gothenburg

HBG

Hiroshima Botanical Garden

NY

William and Lynda Steere Herbarium of the New York Botanical Garden

UB

Laboratoire de Biostratigraphie

H

University of Helsinki

HUEFS

Universidade Estadual de Feira de Santana

CORD

Universidad Nacional de Córdoba

SP

Instituto de Botânica

BHCB

Universidade Federal de Minas Gerais

HAS

Fundação Zoobotânica do Rio Grande do Sul

T

Tavera, Department of Geology and Geophysics

UEC

Universidade Estadual de Campinas

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