Odontonema aliciae T. F. Daniel and J. F. Carrión, 2015

Daniel, Thomas F. & Carrión, Juan F., 2015, Odontonema aliciae, a New Heterostylous Species of Acanthaceae from Panama, Proceedings of the California Academy of Sciences 62 (2), pp. 25-30 : 25-29

publication ID

https://doi.org/ 10.5281/zenodo.11066761

DOI

https://doi.org/10.5281/zenodo.11087646

persistent identifier

https://treatment.plazi.org/id/CD5687C6-FF91-DB13-8C35-176FFD6FFBAF

treatment provided by

Felipe

scientific name

Odontonema aliciae T. F. Daniel and J. F. Carrión
status

sp. nov.

Odontonema aliciae T. F. Daniel and J. F. Carrión View in CoL , sp. nov.

Figure 1. View FIGURE

TYPE.— PANAMA: Veraguas: P.N. Cerro Hoya , Restingue , islote, E800443 , N510434 , 18 Jul 2011 (flr), A. Ibáñez, R. Flores, N. León, J. Domínguez, A. Jiménez, L. Vega, & V. Sánchez 6928 (holotype, PMA; isotypes: CAS, MO). Figure 1. View FIGURE

DIAGNOSIS.— Odontonema aliciae differs from all other Panamanian species of Odontonema by the combination of its subauriculate leaves; short (13–20 mm long) and pink corollas; and glabrous internodes, peduncles, and pedicels.

Shrubs to 1.5 m tall. Young stems subquadrate to quadrate, internodes glabrous, nodes pubescent with a line or arc of flexuose to erect eglandular trichomes 0.2– 0.7 mm long between petioles, trichomes becoming ± deciduous in fruiting plants. Leaves sessile to subsessile, petiole (if present) to 4 mm long, distal blades elliptic to obovate-elliptic to subpandurate, 90–263 mm long, 24–84 mm wide, length:width =2.9–4.5, reduced in size distally to 23 mm long and 3 mm wide, subauriculate at base, attenuate at apex, adaxially glabrous, abaxially pubescent with erect to flexuose eglandular trichomes to 0.7 m long, trichomes sometimes restricted to major veins or deciduous in fruiting plants. Inflorescence of axillary (from distal nodes) and terminal pedunculate thyrses to 115 mm long and 50 mm across near midpoint (including peduncle and excluding corollas/capsules) or sometimes with axillary pedunculate dichasia in axils of some distal leaves, peduncles of thyrses (and dichasia in leaf axils) 11–30 mm long, glabrous, rachis pubescent like young stems, dichasia of thyrses mostly opposite, 2–7 (or more)-flowered, pedunculate, peduncles of dichasia 5–13 mm long, glabrous. Bracts sometimes caducous, lanceolate to subulate, 2.2–8 mm long, 0.4–1.4 mm wide, abaxially glabrous. Bracteoles and secondary bracteoles subulate to lanceolate, 1–3.5 mm long, 0.3–1 mm wide, abaxially glabrous, margin usually ciliate or trichomes deciduous in fruiting plants. Flowers heterostylous, pedicellate, pedicels 4.5–9 mm long, glabrous. Calyx 6.5–9 (– 12 in fruit) mm long, tube 0.5–1.5 (– 2.5 in fruit) mm long, lobes lanceolate to lance-subulate, 5.5–8 (– 10 in fruit) mm long, 0.7–1.1 mm wide, abaxially glabrous. Corolla pink to purple with white marking on lower-central lobe, 13–20 mm long, externally glabrous, internal surface of limb glandular, tube subcylindric 7.5–11 mm long, narrow proximal portion 5–6 mm long, 1.7–2.3 mm in diameter (measured flat), throat inconspicuous, 4–6 mm long, upper lip 6–9.5 mm long, lobes 2.5–3 mm long, lower lip 5.5–11 mm long, lobes 4.8–9.5 mm long. Thrum stamens exserted from mouth of corolla, 5.5–10 mm long, pin stamens included in corolla tube, 3.5 mm long, thecae 2–2.5 mm long, staminodes 2, ca. 1 mm long. Pollen (Hammel 5472) spherical to subspheroidal ( P: E = 0.97–1.00), 3-colporate, 6-pseudocolpate, colpi and pseudocolpi microverrucate, interapertural surfaces reticulate, polar diameter ( P) 30–36 µm, equatorial diameter ( E) 31–36 µm. Ovary glabrous, style pubescent with flexuose eglandular trichomes, thrum style 3.8–4.5 mm long, pin style 12–13 mm long, stigma ± 2-lobed, lobes ca. 0.1 mm long. Capsule 20–30 mm long, glabrous, stipe 7–10 mm long, head 13–17 mm long. Seeds flattened (plano-convex to concavo-convex), flattened surfaces subcordate to subcircular to subsquare in outline, longest axis 6–7.8 mm, shortest axis 4.5–6.3 mm, 1.3–1.7 mm thick, surfaces and margin smooth to slightly roughened.

PHENOLOGY.— Flowering: July–October; fruiting: December.

DISTRIBUTION AND HABITAT.— Panama (Los Santos, Veraguas), on the Azuero Peninsula and islands off the southern coast of Panama to the west of that peninsula ( Fig. 2 View FIGURE ); plants occur on slopes along rocky shoreline and in forests adjacent to beaches at elevations less than 10 m.

ETYMOLOGY.— The specific epithet honors Spanish botanist Alicia Ibánez, who has contributed greatly to the knowledge of the Panamanian flora, especially to that of Coiba National Park and neighboring regions. She also collected the type and co-collected two of the paratypes.

27

IUCN CONSERVATION STATUS.— Odontonema aliciae is presently known from five relatively recent collections (collected between 1978 and 2012) with an extent of occurrence ( EOO) of 4,106 km 2 and an area of occupancy ( AOO; grid cell area of 4 sq. km) of 20 sq. km. In reality, the terrestrial EOO is considerably less than that calculated because a significant part of the EOO consists of approximately 1,500 sq. km of open ocean (but there is potential habitat on small islands that occur in the oceanic region). The linear distances of occurrence are 170 km west to east and 65 km north to south.

Primary threats to the species consist of seaborne events (e.g., tsunamis, hurricanes) and human-mediated coastal habitat deterioration. Given any of these potential threats, the number of locations of this species is less than five. A potentially mitigating factor that might favor the longterm perpetuation of this species is the occurrence of some plants in protected areas (e.g., Ibáñez et al. 6928 occurs in Cerro Hoya National Park; Carrión et al. 543 occurs in Coiba National Park). The other three collections occur in areas lacking official protection, and some of these areas have undergone or will potentially undergo deterioration due to construction of tourist infrastructure in the coastal regions in which the plants occur. According to label information on collections and field observations, at different localities plants varied from the dominant species present (e.g., Ibáñez et al. 6928) to occasional (León et al. 753) to rare (Carrión et al. 543). Based on the number of locations and an inferred decline in the extent and/or quality of habitat in the range of this species, two of the subcriteria would appear to be met for an assessment of Endangered for Odontonema aliciae , given its AOO (i.e., B 2, a, b).

PARATYPES.— PANAMA: Los Santos: Playa Venado , 30 km E of Tonosi on hwy. 50, 30 Oct 1978 (flr), B. Hammel 5472 ( MO, PMA); road along coast, 07°14ʹN, 80°31ʹW, 14 Dec 1995 (frt), M. Nee & T . Andres 46341 ( NY, PMA, US) . Veraguas: PN Coiba, Isla Contreras, Isla Fragata , N416326 . 62, W866367 . 81, 11 Jan 2012 (flr), J. Carrión et al. 543 ( PMA); Golfo de Montijo , Cébaco, E472764 , N826429 , 10 Aug 2011 (flr), N. León et al. 753 ( PMA) .

Neotropical relatives of Odontonema in the Pseuderanthemum lineage of Acanthaceae : Justicieae include several morphologically similar genera: Chileranthemum Oerst. , Oplonia Raf. , Pulchranthus V.M. Baum, Reveal & Nowicke , and Pseuderanthemum Radkl. ex Lindau ( McDade et al. 2000). Morphological distinctions among these genera, all of which contain heterostylous species, are largely based on form of the corolla, which likely reflects adaptation to different predominant pollinators (cf. Daniel 1995, especially fig. 1).

A Colombian species originally described as Odontonema stenostachyum Leonard ( Leonard 1958) and treated as Pseuderanthemum stenostachyum (Leonard) V.A.W. Baum by Baum (1982), belongs to the Pseuderanthemum lineage. Like O. aliciae , it has sessile to subsessile and “more or less subauriculate” leaf blades ( Leonard 1958:392). In the protologue of O. stenostachyum , the corollas were described as immature and an accompanying illustration shows them as buds only; this condition was verified by studying the type collection at US. Because Baum (1982) did not provide a rationale for transferring this species to Pseuderanthemum , and because the differences between these two genera are subtle at best, the generic affinities of P. stenostachyum remain suspect. It can be distinguished from O. aliciae by the characters in the following couplet:

1a. Internodes of vegetative stems and inflorescence rachis, peduncles, and pedicels glabrous; inflorescence broad (ca. 50 mm across near midpoint) with dichasia pedunculate; calyx 6. 5–9 mm long; corolla pink to purple with white markings on lower-central lobe; seeds with longest axis 6.5–7. 5 mm ............................................. Odontonema aliciae View in CoL

1b. Internodes of vegetative stems and inflorescence rachis, peduncles, and pedicels pubescent; inflorescence narrow (ca. 20 mm across near midpoint) with dichasia sessile to subsessile; calyx 4–5 mm long; corolla white; seeds with longest axis ca. 3 mm long.............................................................. Pseuderanthemum stenostachyum View in CoL

Among Mexican and Central American Odontonema , O. auriculatum (Rose) T.F. Daniel is also morphologically similar and is perhaps a closer relative of O. aliciae . Odontonema auriculatum occurs in western Mexico, from Sinaloa to Oaxaca, where plants grow in tropical deciduous and tropical subdeciduous forests at elevations from 60–230 m (Daniel 1995). That species is characterized by the combination of its conspicuously auriculate leaves and red flowers (Daniel 1995). It can be further distinguished from O. aliciae by the characters and distributions summarized in the following couplet:

1a. Corolla pink to purple, 13–20 mm long, tube 7.5–11 mm long, subcylindric, throat inconspicuous (i.e., not well differentiated from narrow proximal portion of tube); calyx 6.5–9 mm long, lobes, 5.5–8 mm long; dichasia pedunculate, peduncles 5–13 mm long; leaves sessile to subsessile (i.e., with naked petiole to 4 mm long), subauriculate at base; Panama.... O. aliciae View in CoL

1b. Corolla red, (20–) 25–30 mm long, tube 13–20 mm long, funnelform, throat conspicuous; calyx 2–5 mm long, lobes 1.4–4 mm long; dichasia sessile to pedunculate, peduncles 1–4 mm long; leaves sessile, conspicuously auriculate at base; Mexico................. O. auriculatum View in CoL

Like many other species of Odontonema View in CoL , O. aliciae View in CoL is distylous with some individuals having long stamens and short styles (thrum flowers; e.g., Ibáñez et al. 6928 at PMA-plant on left side of sheet) whereas others have shorter stamens and longer styles (pin flowers; e.g., Hammel 5472 at PMA). Although floral visitors were not observed to O. aliciae View in CoL , the flowers are suggestive of those often pollinated by hummingbirds and/or bees. Corolla color varies from pink (e.g., Ibáñez et al. 6928) to purple (e.g., Carrión et al. 543). Pollen of O. aliciae View in CoL is of the basic type common to most species of the genus (i.e., 3-colporate, 6-pseudocolpate; Fig. 3 View FIGURE ) and to the Pseuderanthemum View in CoL lineage ( Baum 1982; Daniel 1998; McDade et al. 2000).

CAS

USA, California, San Francisco, California Academy of Sciences

PMA

Provincial Museum of Alberta

CAS

California Academy of Sciences

MO

Missouri Botanical Garden

P

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

E

Royal Botanic Garden Edinburgh

A

Harvard University - Arnold Arboretum

B

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

M

Botanische Staatssammlung München

T

Tavera, Department of Geology and Geophysics

NY

William and Lynda Steere Herbarium of the New York Botanical Garden

J

University of the Witwatersrand

N

Nanjing University

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