PhytoKeys 39: 1–17, doi: 10.3897/phytokeys.39.7668
Three new caespitose species of Senecio (Asteraceae, Senecioneae) from South Peru
Daniel B. Montesinos Tubée 1,2,3
1 Nature Conservation & Plant Ecology Group, Wageningen University, Netherlands. Droevendaalsesteeg 3a, 6708PB Wageningen, The Netherlands
2 Naturalis Biodiversity Centre, Botany Section, N
3 ational Herbarium of The Netherlands, Herbarium Vadense. Darwinweg 2, 2333 CR Leiden, The Netherlands
4 Instituto Científico Michael Owen Dillon, Av. Jorge Chávez 610, Cercado, Arequipa, Perú

Corresponding author: Daniel B. Montesinos Tubée (dbmtperu@gmail.com; daniel.montesinos@wur.nl)

Academic editor: A. Sennikov

received 8 April 2014 | accepted 3 June 2014 | Published 19 June 2014
(C) 2014 Daniel B. Montesinos Tubée. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
For reference, use of the paginated PDF or printed version of this article is recommended.

Citation: Montesinos Tubée DB (2014) Three new caespitose species of Senecio (Asteraceae, Senecioneae) from South Peru. PhytoKeys 39: 1–17. doi: 10.3897/phytokeys.39.7668

Abstract

Three new species of the genus Senecio (Asteraceae, Senecioneae) belonging to Senecio ser. Suffruticosi subser. Caespitosi were discovered in the tributaries of the upper Tambo River, Moquegua Department, South Peru. Descriptions, diagnoses and discussions about their distribution, a table with the morphological similarities with other species of Senecio, a distribution map, conservation status assessments, and a key to the caespitose Peruvian species of Senecio subser. Caespitosi are provided. The new species are Senecio moqueguensis Montesinos, sp. nov. (Critically Endangered) which most closely resembles Senecio pucapampaensis Beltrán, Senecio sykorae Montesinos, sp. nov. (Critically Endangered) which most closely resembles Senecio gamolepis Cabrera, and Senecio tassaensis Montesinos, sp. nov. (Critically Endangered) which most closely resembles Senecio moqueguensis Montesinos.

Resumen

Tres nuevas especies del género Senecio (Asteraceae, Senecioneae) pertenecientes a Senecio ser. Suffuticosi subser. Caespitosi fueron descubiertas en las alturas de la cuenca del río Alto Tambo, Departamento Moquegua, Sur de Perú. Las especies se describen y tipifican, una diagnosis y discusión acerca de su distribución, una tabla con las similitudes morfológicas con otras especies de Senecio, un mapa de distribución, el estatus de conservación y una clave para las especies peruanas cespitosas de Senecio subser. Caespitosi son presentadas. Las nuevas especies son Senecio moqueguensis Montesinos, sp. nov. (En Peligro Crítico) el cual se asemeja más a Senecio pucapampaensis Beltrán, Senecio sykorae Montesinos, sp. nov. (En Peligro Crítico) el cual se asemeja más Senecio gamolepis Cabrera, y Senecio tassaensis Montesinos, sp. nov. (En Peligro Crítico) el cual se asemeja más a Senecio moqueguensis Montesinos.

Keywords

Compositae, new species, Senecio subser. Caespitosi, South America, taxonomy

Introduction

Senecio contains about 175 species in Peru (Brako and Zaruchi 1993, Vision and Dillon 1996) including several recently described new species (Beltrán 2009). The genus has 94 species endemic to Peru which have been evaluated and classified according to IUCN criteria (Beltrán et al. 2007). In the Department of Moquegua, 30 species have been recorded (Arakaki and Cano 2003, Montesinos 2012). The species of Senecio described here were discovered in the tributaries of the upper Tambo River in southern Peru, an area of extraordinary species richness and a high level of endemism (Montesinos 2011, 2012).

Senecio ser. Suffruticosi Cabrera accounts for 143 species occurring on the American continent, especially in the Andes and Patagonia (Cabrera 1949, Cabrera 1985, Cabrera et al. 1999). Cabrera et al. (1999) divided Senecio ser. Suffruticosi into five subseries and described it as embracing suffruticose or perennial herbs, glabrous or glandulose, with entire leaves which are dentate or, more rarely, incised, involucres discoid, and capitula isomorphic. Among those subseries, Senecio subser. Caespitosi Cabrera contains 50 species (Cabrera et al. 1999), of which thirteen occur in Peru at altitudes between 3500 m and 5000 m (Brako and Zaruchi 1993, Beltrán et al. 2007): Senecio adenophyllus Meyen & Walp., Senecio algens Wedd., Senecio scorzonerifolius Meyen & Walp. and Senecio trifurcifolius Hieron. also distributed in northwestern Argentina, Bolivia and north of Chile, Senecio danai A. Gray and Senecio pucapampaensis Beltrán occurring only in central Peru (Beltrán et al. 2007), Senecio evacoides Sch. Bip., Senecio expansus Wedd. and Senecio humillimus Sch. Bip. also distributed in northwestern Argentina and Bolivia, Senecio gamolepis Cabrera, endemic to central and southern Peru, Senecio rufescens DC. distributed from Colombia to northwestern Argentina, Senecio repens Stokes distributed from south Ecuador through Peru and northwestern Bolivia, and Senecio vegetus (Wedd.) Cabrera, also distributed in Bolivia. In Senecio subser. Caespitosi plants are characterized as suffruticose (or herbaceous), glabrous or glandulose; leaves entire, dentate or, more rarely, incised; capitula discoid, medium or small; and flowers isomorphic (Cabrera et al. 1999).

Notwithstanding the progress in taxonomical and molecular studies (Nordenstam 1977, Cabrera 1949, 1985, Cabrera et al. 1999, Pelser et al. 2007, Nordenstam et al. 2009), there are more species of the tribe Senecioneae occurring in the Andes which remain poorly understood and are awaiting discovery. Intergeneric relationships within Senecioneae are still largely unknown (Pelser et al. 2007); furthermore, the lack of knowledge about generic-level evolutionary relationships in Senecioneae remains the largest taxonomic problem on the way to obtaining a monophyletic delimitation of Senecio (Bremer 1994, Pelser et al. 2007). Phylogenetic positions for the members of Senecio subser. Caespitosi are still largely unknown, except for Senecio algens, Senecio humillimus and Senecio rufescens (Pelser et al. 2007), of which Senecio algens belongs to the Aetheolaena involucrata-Aetheolaena patens clade and Senecio humillimus and Senecio rufescens to the Senecio glaber-Senecio donianus clade. Numerous new collections from Moquegua have been made in recent years (Montesinos 2011, 2012). A comparison with herbarium specimens, together with a review of the literature and taxonomic keys, has shown that these collections include three new species of Senecio subser. Caespitosi which are described below. These new species were separated from the other species of this subseries on the basis of a set of characters such as habit, the presence or absence of trichomes, flower color, the number of phyllaries and involucral bracts, the involucre length and the achene type (Cabrera 1955, 1985, Cabrera et al. 1999). The new species can be found at elevations above 4500 m as terrestrial plants on bare rocky soils on the summits of high mountains in the north of Moquegua department, where they co-occur with several other acaulescent Senecioneae from Senecio subser. Caespitosi such as Senecio gamolepis, Senecio evacoides, and Senecio algens.

Methods

Based on morphological characters, an overview of the genus Senecio with an emphasis on Senecio subser. Caespitosi from Peru and adjacent areas (Ecuador, Bolivia, Argentina and northern Chile) has been prepared, based on Cabrera (1955, 1985) and Cabrera et al. (1999). Since 2009 I have examined more than 450 specimens of Senecio subser. Caespitosi housed in Peruvian herbaria (CUZ, HSP, HUPCH, HUSA, MOL, USM), relevant collections from institutions abroad (B, BR, F, L, LPB, MO, P, WAG), and material from my recent fieldwork. Digitised specimens were viewed via online herbarium catalogues (http://tropicos.org and http://fm1.fieldmuseum.org/vrrc/) or via JSTOR (2013). All morphological characters were studied under a NSZ-405 1X-4.5X stereo microscope and an AmScope M100C-LED 40×-1000× compound microscope. The descriptions were made using the terminology presented by Cabrera (1955, 1985), Cabrera et al. (1999), Vision and Dillon (1996), Beltrán (2009), Nordenstam et al. (2009) and Roque et al. (2009). Conservation assessments were undertaken using the IUCN criteria (IUCN 2001).

Taxonomy
Senecio moqueguensis Montesinos, sp. nov.

urn:lsid:ipni.org:names:77140249-1

Figs 1, 4A, 5
Diagnosis.

The new species is morphologically similar to Senecio pucapampaensis but is clearly distinguished by the leaf lamina oblong-spathulate (vs. cuneiform), leaf surface covered by thin trichomes (vs. glabrous), corolla yellow (vs. white), calycular bracts linear-oblong, 6–9 mm long (vs. linear, 6–7 mm long), and phyllaries 9–12 (vs. 12–14).

Type.

PERU. Moquegua Region, General Sánchez Cerro Province, Ubinas District, NW of Tassa, terrestrial on clayey rocky soils on the plateau peaks near Lake Pacosani, elevation 4653 m, 16°06'43"S, 70°44'45"W, 3 April 2009, Montesinos 2400 (holotype USM!, isotypes MO 2383567, HUPCH 4185, CPUN, WAG 0246107).

Description.

Perennial herb, rhizomatous, creeping, low-growing, forming mats 2–4 cm tall and up to 60 cm in diam. Trichomes glandular, somewhat dense and irregularly distributed, multicellular, whitish transparent, 0.1–0.3 mm long and 0.05–0.1 mm wide and composed of 4–8 subrotund cells (each 30–50 µm long), apical cell rotund. Stems 1–3 cm long, often densely branched and leafy in the central part, rooting. Leaves cauline, lamina oblong-spathulate, 8–12 mm × 1–2.5 mm, sparsely covered by thin trichomes on the margins, lower and upper surfaces except at the base; base truncated, apex subpinnatifid; young leaves dark green with yellowish margins, turning light green-greyish with age. Synflorescences of solitary sessile or subsessile terminal capitula. Capitula homogamous, discoid. Involucres at first broadly cylindrical, gradually turning campanulate with age, ca. 7–10 mm long × 6–8.5 mm wide). Calycular bracts linear-oblong (6–9 mm × 1–2.5 mm), whitish green on the surface and whitish along the margins, with scarce trichomes near the midrib and margins, apex dark brown covered with short light-brown trichomes. Phyllaries 9–12, connate, 5–8 mm long × 0.7–1.2 mm wide, oblong-lanceolate, covered with thin trichomes sparsely on the surface and densely along the margins, apex greenish grey and dark brown with short white multicellular trichomes. Florets 24–28; corolla tubular, abruptly constricted near the base, 5-lobed, each lobe 0.5 mm long, bright yellow, tube 3–5 mm long × 0.8–1 mm wide; anthers linear-lanceolate, 1.5–2.5 mm long, 0.2–0.4 mm wide, ecalcarate, terminal appendages lanceolate, obtuse, margin whitish transparent and becoming yellow towards the centre; style dark yellow, truncate, papillae covering the whole surface of the apex. Achenes cylindrical, covered with trichomes, 1.8–2.5 mm long and 0.4–0.8 mm wide, light brown; carpopodium symmetrical in a small ring; pappus of smooth bristles, white, silky, 5–6 mm long, with fine single setulae.

Figure 1.

Senecio moqueguensis Montesinos. A Leaf (upper side) B Leaf (underside) C Phyllary trichomes D Leaf trichomes E Capitulum F Calycular bracts G Phyllary H Stamens arrangement in a floret I Floret J Pappus bristles K Stamens L Style M Papillose stigma N Achene

Ecology and distribution.

Terrestrial plant on clayey rocky soils on the peaks of the highland summits and grasslands in the north of Moquegua Region, at elevations of ca. 4500 to 4800 m. Co-occurring species include Azorella compacta Phil., Calamagrostis vicunarum (Wedd.) Pilg., Pycnophyllum molle Remy, and Festuca spp. Flowers and fruits between March and April.

Etymology.

The specific epithet refers to Moquegua, where the only three collections are known from the north of the department.

Additional material examined

(paratypes). PERU. Moquegua Region, General Sánchez Cerro Province, Ubinas District, terrestrial on bare clayey soils in the verges of the road east Pillone town, elevation 4584 m, 16°10'02"S, 70°49'56"W, 24 March 2013, Montesinos 4022 (USM, HUSA). Moquegua Region, General Sánchez Cerro Province, Ubinas District, NW of Tassa, terrestrial on bare clayey soils in the verges of the road to Lake Cochapata, elevation 4687 m, 16°08'56"S, 70°43'0.30"W, 9 December 2013, Montesinos 4200 (CUZ).

Discussion.

A comparison of the material has shown that Senecio moqueguensis is most similar to Senecio pucapampaensis and Senecio tassaensis sp. nov. Together with Senecio evacoides, Senecio expansus, Senecio repens and Senecio humillimus, it forms a coherent morphological and geographical group within Senecio subser. Caespitosi which occurs from central Peru to northwest Argentina and is characterized by the presence of trichomes on stems, leaves and involucres. Senecio moqueguensis can be distinguished from Senecio pucapampaensis by the dense caespitose mat habit, leaves, calycular bracts, corolla color, involucres and achene morphology as summarised in Table 1. Senecio moqueguensis can be distinguished from Senecio evacoides, Senecio expansus and Senecio repens by the habit, density of trichomes, leaf shape and length, as well as by the calycular bracts and phyllary length and form.

Table 1.

Comparison between Senecio moqueguensis, Senecio sykorae, Senecio tassaensis and their closest relatives.

Senecio moqueguensis Senecio sykorae Senecio tassaensis Senecio pucapampaensis Senecio gamolepis Senecio algens Senecio evacoides Senecio humillimus Senecio expansus Senecio trifurcifolius Senecio repens
Distribution PE (Moquegua) PE (Moquegua) PE (Moquegua) PE (Junin) PE, CH, AR, BO PE, BO, AR PE, BO, AR BO, South Peru AR, BO, PE PE, BO, CH BO, EC, PE
Altitude 4500–4800 m 4550–4800 m 4650–4700 m 4500–4600 m 4000–4800 m 4500–5000 m 4000–4800 m 3500–4500 m 3900–4800 m 4000–4500 m 3000–4600 m
Habit dense caespitose mat tuft mat tuft postrate, decumbent dense caespitose mat caespitose subshrub suffruticose or shrubby dense caespitose mat ground rosette herb suffruticose ground rosette herb
Plant dimensions (height, diameter) 2–4 cm, > 60 cm 4–6 cm, > 6 cm 2–4 cm, > 4 cm 5–9 cm, > 8 cm 2–3 cm, > 1 m 4–6 cm, > 6 cm 2 cm, ca. 1 m 2 cm, ca. 70 cm 2–4 cm, 5–8 cm 5–8 cm, > 8 cm 2–4 cm, 6–9 cm
Indumentum glandular, multicelular, 0.1–0.3 mm absent glandular, multicelular, 0.3–1.2 mm finely puberulous, <0.1 mm absent absent white lanuginose, < 0.2 mm puberulous, 0.1–0.2 mm densely lanuginose, < 0.2 mm absent puberulous, < 0.2 mm
Leaf shape oblong-spathulate, subpinnatifid obovate-spathulate obovate-spathulate, incised or acuminate cuneiform-subpinnatifid, incised linear-lanceolate spathulate, obtuse obovate-spathulate linear-spathulate, ovate ovate, elliptical or circular, crenate cuneiform-linear, dentate elliptic-ovate, obovate
Leaf (length, width) 8–12 × 1–2.5 mm 9–14 × 1–2.2 mm 6–9 × 1–2.5 mm 9–15 × 3–4 mm 8–12 × 2–4 mm 10–35 × 2–5 mm 10–20 × 3–6 mm 3–10 × 0.5–1 mm 10–25 × 10–22 mm 10–20 × 1 mm 10–25 × 10–22 mm
Leaf pubescence sparsely covered by thin trichomes glabrous densely covered by trichomes ciliate margins glabrous glabrous densely lanuginose sparsely puberulous densely lanuginose glabrous glabrous adaxially, puberulous abaxially
Involucre (shape; length; width) cylindrical-campanulate; 7–10 × 6–8.5 mm cylindrical-campanulate; 7–9 × 3–5 mm cylindrical-campanulate; 6–8 × 5–7 mm campanulate; 7–8 × 8–9 mm cylindrical-campanulate; 8–11 × 4–6 mm cylindrical-campanulate; 7.5–10 × 8–12 mm campanulate; 7–8 × 5–6 mm cylindrical-campanulate; 5 × 3–4 mm campanulate; 10–25 × 10–22 mm campanulate; 8–9 × 6 mm campanulate; 6–7 × 8–10 mm
Calycular bracts (shape; margin; size) linear-oblong; sparse trichomes; 6–9 × 1–2.5 mm linear-oblong; scarce trichomes; 6–8 × 0.7–1 mm ovate-oblong; dense trichomes; 4–6 × 1 mm linear; ciliate; 6–7 × 1 mm linear; glabrous; 7–10 × 0.8–1.2 mm linear; glabrous; 6–9 × 0.8–1.1 mm linear; tomentose; 6–7 × 0.8–1.2 mm linear; glabrous; 3–4 × 0.7–1 mm linear; tomentose; 9–22 × 2.5–5 mm linear, glabrous; 7–8 × 0.8–1.2 mm linear, glabrous; 5–6 × 0.8–1.2 mm
Phyllaries (shape; size) oblong-lanceolate; 5–8 × 0.7–1.2 mm linear-lanceolate; 5–6.5 × 0.6–1 mm linear-lanceolate; 5–8 × 0.8–1.2 mm linear; 6–7 × 1.2 mm oblong; 6–8 × 1.8–2.3 mm linear; 7–9 × 2–3 mm linear; 5–7 × 0.8–1.1 mm oblong-lanceolate; 6–8 × 1–1.2 mm linear; 10–15 × 2–4 mm lanceolate, attenuate; 6–8 × 1–1.5 mm linear; 13–20 mm × 1–2 mm
Phyllaries (number) 9–12 12–14 12–16 12–14 7–9 10–15 13–20 8 20–25 8 13–20
Phyllaries (margins) densely covered with trichomes glabrous densely covered with trichomes scarious, ciliate glabrous glabrous pubescent glabrous glabrous or pubescent glabrous glabrous
Corolla (color) bright yellow white purple-pink to pale white white yellow yellow yellow dark yellow with purple tube yellow yellow yellow
Achene (shape, texture) cylindrical, with trichomes cylindrical, with trichomes ovate, striate, with trichomes cylindrical, glabrous cylindrical, glabrous cylindrical, glabrous cylindrical, glabrous cylindrical, sericeous cylindrical, glabrous cylindrical-ovate, densely sericeous cylindrical, glabrous
Pappus (length) 5–6 mm 4–6 mm 3.5–5 mm 5–6 mm 6–9 mm 6–8 mm 4–6 mm 5–7 mm 10–20 mm 6–7 mm 5–6 mm
Conservation status.

Following the criteria and categories of IUCN (2001), a preliminary status of Critically Endangered (CR) is assigned. The new species deserves protection because its total area of occupancy is less than 100 km² (ca. 50 km²) (B1); only three populations are known (B1b); habitat inferred to be continuing to decline (B1b(i-iii)); population estimated to number fewer than 300 individuals (D). The suitable habitats for Senecio moqueguensis on the mountain summits near the set of lakes in the Ubinas district are regarded as endangered because overgrazing of grasslands, changes in annual rainfall, volcanic activity, and exploitation of natural resources may all potentially reduce their extent.

Senecio sykorae Montesinos, sp. nov.

urn:lsid:ipni.org:names:77140250-1

Figs 2, 4B, 5
Diagnosis.

Morphologically similar to Senecio gamolepis but clearly distinguished by the tuft mat habit (vs. cushion mats), the leaf shape being obovate-spathulate (vs. linear-lanceolate), corolla white (vs. yellow), phyllaries 12–14 (vs. 7–9), disc length 7–9 mm (vs. 8–12 mm), and achene length 1.5–2 mm (vs. 1–1.3 mm).

Type.

PERU: Moquegua Region, General Sánchez Cerro Province, Yunga District, E of Yunga, terrestrial on bare clayey soils on the peaks of Perusa mountain, elevation 4802 m, 16°11'08"S, 70°38'14"W, 13 April 2012, Montesinos & Calisaya 3805 (holotype USM!, isotype HUSA!).

Description.

Perennial herb, decumbent, low-growing and forming small tuft mats 4–6 cm high and up to 6 cm in diam. Trichomes absent. Stems 3–5 cm long, densely leafy, woody and branched at the base. Leaves cauline, alternate, lamina obovate-spathulate, 9–14 mm long × 1–2.2 mm wide, glabrous on surface and margins except at the base (scarcely covered by thin, short trichomes), base truncate to auriculate, apex obtuse, entire, margin involute; young leaves pale green with yellowish margins turning dark green with age. Synflorescences of solitary, terminal capitula. Capitula homogamous, discoid and pedicled (5–10 mm long). Involucres at first narrowly cylindrical becoming cylindrical-campanulate with age (7–9 mm long × 3–5 mm wide). Calycular bracts linear-oblong (6–8 mm × 0.7–1 mm), dark green on the surface and light green along the margins, with dark brown-black apex covered with inconspicuous trichomes or glabrous. Phyllaries 12–14, connate, 5–6.5 mm long × 0.6–1 mm wide, linear-lanceolate, margins glabrous, apex dark brown with short trichomes. Florets 13–16; corolla tubular, abruptly constricted near the base, 5-lobed, each lobe 0.2–0.3 mm long, white, tube 2.5–4 mm long × 0.5–0.8 mm wide; anthers linear-lanceolate, 1.5–2 mm long × 0.2–0.3 mm wide, truncate, terminal appendages lanceolate, obtuse; margin whitish transparent and becoming darker towards the centre; style dark purple, truncate, apically covered by papillae equally distributed. Achenes cylindrical, pale green, finely covered with trichomes, 1.5–2 mm long × 0.6–0.9 mm wide; carpopodium symmetrical in a shallow ring; pappus of smooth fine bristles, white, 4–6 mm long, with fine alternate single setulae.

Figure 2.

Senecio sykorae Montesinos. A Leaf (upper side) B Leaf (underside) C Capitulum D Calycular bracts E Phyllary F Stamens arrangement in a floret G Floret H Pappus bristles I Stamens J Style K Papillose stigma L Achene

Ecology and distribution.

Terrestrial plant on bare clayey soils on the summits of mountain peaks and grassland plateaus in the north of the Moquegua Region at elevations of 4550–4800 m. Co-occurring with Belloa pickeringii (A. Gray) Sagást. & M.O. Dillon, Nototriche obcuneata (Baker f.) A.W. Hill, Pycnophyllum molle Remy, Senecio candollei Wedd. and Xenophyllum ciliolatum (A. Gray) V.A. Funk. Flowers and fruits between March and April.

Etymology.

This Senecio is named after Karlè Sýkora, a well-known Dutch vegetation scientist who was my mentor in phytosociology.

Additional material examined

(paratypes). PERU. Moquegua Region, General Sánchez Cerro Province, Ubinas District, S of Pillone, terrestrial on bare clayey soils in the verges of the road to Pillone town, elevation 4584 m, 16°10'02"S, 70°49'56"W, 24 March 2013, Montesinos 4023 (USM).

Discussion.

Senecio sykorae appears to be closely related to Senecio gamolepis which grows at higher elevations but approaches the known range of Senecio sykorae within a few hundred metres. While Senecio gamolepis is generally distinctive in the genus for its large size, attaining widths of up to 1 meter in diameter, and for its larger, capitulate form, Senecio sykorae is a smaller plant, of about 4–6 cm wide and has shorter corolla, less than 9 mm long. Senecio sykorae is also distinctive in that it has 12–14 phyllaries per capitulum instead of 7–9 phyllaries in Senecio gamolepis. Likely the leaves of Senecio sykorae are distinctive in that they are obovate-spathulate vs. linear-lanceolate. Also, the achenes in Senecio sykorae are larger (1.5–2 mm long) vs. 1–1.3 mm long in Senecio gamolepis. Senecio sykorae also differs from Senecio algens by the leaf and capitula length (shorter in Senecio sykorae), and from both species by the corolla colour (white vs. yellow). Less similarity is found in Senecio algens, Senecio humillimus, Senecio trifurcifolius, Senecio pucapampaensis and Senecio evacoides, and from which Senecio sykorae can be distinguished on the basis of its habit, trichomes, leaf shape and length, calycular bracts and phyllary length and shape as summarized in Table 1.

Conservation status.

Following the criteria and categories of IUCN (2001), a preliminary status of Critically Endangered (CR) is assigned. The new species deserves protection because its total area of occupancy is less than 10 km² (ca. 5 km²) (B2); only one population known (B2b); habitat inferred to be continuing to decline (B2b(i-iii)); population estimated to number fewer than 150 individuals (D). The suitable habitats for Senecio sykorae on the mountain summits of the north of Moquegua are indicated as endangered because of overgrazing of grasslands, changes in annual rainfall, volcanic activity, and exploitation of natural resources, all potentially reducing their extent.

Senecio tassaensis Montesinos, sp. nov.

urn:lsid:ipni.org:names:77140251-1

Figs 3, 4C, 5
Diagnosis.

Similar to Senecio moqueguensis but clearly distinguished by the leaf lamina obovate-spathulate (vs. oblong-spathulate), leaf length 6–9 mm (vs. 8–12 mm), leaf surface densely covered by trichomes (vs. sparsely covered), trichomes 0.3–1.2 mm long (vs. 0.1–0.3 mm long), corolla white (vs. yellow), calycular bracts 4–6 mm long (vs. 6–9 mm), phyllaries 12–16 (vs. 9–12), involucre length 6–8 mm (vs. 7–10 mm), and achene length 1–1.2 mm (vs. 1.8–2.5 mm).

Type.

PERU. Moquegua Region, General Sánchez Cerro Province, Ubinas District, NW of Tassa, terrestrial on clayey rocky soils on the summits of Pirhuani peak, elevation 4657 m, 16°09'58"S, 70°43'49"W, 07 April 2011, Montesinos 3103 (holotype HUSA!, isotypes MOL, USM).

Description.

Perennial herb, tufted, up to 2–4 cm high and up to 4 cm in diam. Trichomes glandular, densely covering the plant, multicellular, whitish transparent, 0.3–1.2 mm long × 0.1–0.2 mm wide, composed of 6–10 ovate or elongate cells (each 60–80 µm long), apical cell rotund. Stems thick, < 1 cm long, often densely branched and leafy in the central portion. Leaves arranged in irregular rosettes, lamina obovate-spathulate, 6–9 mm × 1–2.5 mm, densely covered by thin trichomes on the margins; base truncated and apex pinnatifid; lower and upper surface of the leaves gradually becoming shorter towards the tip; margin incised with 5–7 obtuse lobes or rarely acuminate; mature leaves with involute margins; young leaves green yellow turning greenish grey with age. Synflorescences of solitary sessile or subsessile terminal capitula. Capitula homogamous, discoid. Involucres at first cylindrical, turning campanulate with age (ca. 6–8 mm long × 5–7 mm wide). Calycular bracts ovate-oblong (4–6 mm × 1 mm), greyish green on the surface and covered with trichomes on the margins, dark brown apex covered apically with short brown multicellular trichomes. Phyllaries 12–16, connate, 5–8 mm long × 0.8–1.2 mm wide, linear-lanceolate, covered with thin trichomes scarcely on the surface and densely along the margins, apex dark brown and covered with short multicellular trichomes. Florets 18–21, corolla tubular, abruptly constricted near the base, 5-lobed, each lobe 0.2–0.4 mm long, purple pink gradually becoming pale white towards the tip, tube 2–2.5 mm long × 1 mm wide; anthers linear-lanceolate, 1.5–2 × 0.3–0.4 mm, terminal appendages lanceolate, acute to somewhat protuberant, bases ecalcarate; anthers margin white becoming dark yellow towards the centre; style dark purple, truncate, papillae covering the whole surface of the apex. Achenes ovate, striate, covered with trichomes, 1–1.2 mm long and 0.6–0.8 mm wide, pale yellow; carpopodium symmetrical in a shallow ring; pappus of smooth bristles, white, silky, 3.5–5 mm long, with fine single setulae.

Figure 3.

Senecio tassaensis Montesinos. A Leaf (upper side) B Leaf (underside) C Phyllaries trichomes D Leaf trichomes E Capitulum F Calycular bracts G Phyllary H Stamens arrangement in a floret I Floret J Pappus bristles K Stamens L Style M Papillose stigma N Achene.

Figure 4.

Habit photographs of: A Senecio moqueguensis B Senecio sykorae C Senecio tassaensis.

Figure 5.

Distribution map showing collection and recorded sites for Senecio moqueguensis (red circles), Senecio sykorae (yellow squares) and Senecio tassaensis (green triangles). Inset: Photograph of the highland plains of Tassa, Moquegua, where populations of Senecio moqueguensis occur.

Ecology and distribution.

Terrestrial plant on clayey rocky soils on the peaks of the highland summits of the Pirhuani peak, near Tassa town, Moquegua Region, at elevations of 4650–4700 m. It occurs with Azorella, Calamagrostis, Pycnophyllum, Mniodes, Senecio, and Xenophyllum. Flowers and fruits between March and April.

Etymology.

This Senecio is named after the town of Tassa (Moquegua Region), downslope of Pirhuani peak where the species was found.

Discussion.

Senecio tassaensis appears to be closely related to Senecio moqueguensis which grows at the same elevational range but approaches the known range of Senecio tassaensis within a few hundred metres. Senecio moqueguensis is generally distinctive in the series for its larger size, attaining dense ground mats, and for its yellow corolla. Senecio tassaensis has 12–16 phyllaries (vs. 9–12), an involucre length of 6–8 mm and achene length of 1–1.2 mm, being much shorter than in Senecio moqueguensis. Senecio tassaensis is relatively a very rare species with an estimated 100 individuals known. It is less similar to Senecio pucapampaensis, Senecio evacoides, Senecio expansus and Senecio repens, and can be distinguished on the basis of the habit, trichomes, leaf shape and length, calycular bracts and phyllaries length and shape as summarized in Table 1.

Conservation status.

Following the criteria and categories of IUCN (2001), a preliminary status of Critically Endangered (CR) is assigned. The new species deserves protection because its total area of occupancy is less than 10 km² (ca. 5 km²) (B2); only one population is known (B2b); habitat inferred to be continuing to decline(B2b(i-iii)); population estimated to number fewer than 100 individuals (D). The suitable habitats for Senecio tassaensis on the mountain summits of Pirhuani peak in the Ubinas district are indicated as endangered, because changes in the annual rainfall, volcanic activity and exploitation of natural resources, may all reduce their extent.

Key to the species of Senecio ser. Suffruticosi subser. Caespitosi in Peru

(adapted from Cabrera 1985, Cabrera et al. 1999)

1a Plants shrubby; involucres longer than 11 mm 2
1b Plants caespitose; involucres shorter than 11 mm long 5
2a Achenes densely pubescent; leaves 1–2 cm long, deeply dentate or lobulate Senecio adenophyllus
2b Achenes glabrous; leaves 1–3.5 cm long, entire 3
3a Leaves 3–5 mm wide; involucre bracts oblong Senecio rufescens
3b Leaves 0.7–2 mm wide; involucre bracts linear 4
4a Leaves 25–80 mm long; phyllaries 13–18 Senecio scorzonerifolius
4b Leaves 15–25 mm long; phyllaries 15–20 Senecio danai
5a Capitulum small; involucre shorter than 5 mm 6
5b Capitulum larger; involucre shorter than 11 mm 7
6a Leaves entire, glabrous and fleshy; phyllaries 8 Senecio humillimus
6b Leaves entire or dentate, glabrous or lanuginose; phyllaries 13 Senecio vegetus
7a Plants tomentose, at least on the underside of leaves 8
7b Plants glabrous 13
8a Plants with dense pubescence covering all plant parts 9
8b Plants with sparse pubescence not covering all plant parts 11
9a Leaves spathulate, 10–20 mm long; involucre 7–8 mm tall; phyllaries 13–20 Senecio evacoides
9b Leaves ovate, elliptic or circular, crenate, 10–65 mm long; involucre 6–10 mm tall; phyllaries 13–25 10
10a Involucre 10–25 mm long; phyllaries 20–25 Senecio expansus
10b Involucre 6–7 mm long; phyllaries 13–20 Senecio repens
11a Leaves cuneiform, lamina glabrous except puberulous margins Senecio pucapampaensis
11b Leaves oblong, lamina with trichomes on surfaces and margins 12
12a Leaves 8–12 mm long, lamina oblong-spathulate; involucre 7–10 mm; phyllaries 9–12 Senecio moqueguensis
12b Leaves 6–9 mm long, lamina obovate-spathulate; involucre 6–8 mm; phyllaries 12–16 Senecio tassaensis
13a Leaves dentate, linear-cuneiform Senecio trifurcifolius
13b Leaves entire 14
14a Leaves 10–35 mm long Senecio algens
14b Leaves less than 14 mm long 15
15a Leaves 8–12 mm, linear-lanceolate; involucre 8–11 mm; phyllaries 6–8 Senecio gamolepis
15b Leaves 9–14 mm, obovate-spathulate; involucre 7–9 mm; phyllaries 12–14 Senecio sykorae
Acknowledgements

I acknowledge Edwin Banegas and Cristian Tejada for field work support; Fabio Calisaya and Esteban Mamani for their hospitality; Hamilton Beltrán and Arturo Granda for their taxonomic comments; John Birks, Blanca León, Pieter Pelser and Jan Wieringa for their valuable observations on the manuscript; two anonymous reviewers for their constructive comments, which helped to improve the manuscript; Delsy Trujillo for the illustrations; Theo Damen, John Pruski, Lauren Peters and Karen Ventura for facilitating the barcodes of the collections at WAG, MO, and HUPCH; Benjamin DeVries for map image support; The Dirección General Forestal y de Fauna Silvestre (DGFFS) for permits to collect outside protected areas; the herbaria B, BR, CUZ, F, HSP, HUPCH, HUSA, L, LPB, MO, MOL, P, USM, and WAG for providing access to their material; Cuzzi y Cía., S.A. for facilitating the scanning of images; and Ruben Sierra for assisting with the literature. This work was done as part of the phytosociological studies sponsored by Alberta Mennega Stichting and Hugo de Vries Fonds, the Netherlands. The language editor was Joy Burrough.

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