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Research Article
Octoblepharum peristomiruptum (Octoblepharaceae) a new species from the Neotropics
expand article infoNoris Salazar Allen, José A. Gudiño
‡ Smithsonian Tropical Research Institute, Ancón Panama, Panama
Open Access

Abstract

Octoblepharum peristomiruptum, a new species of moss in the family Octoblepharaceae from Panama and Brazil, is described and illustrated. The new species is characterised by plants with a reddish-purple colour particularly at the leaf bases, peristomes of eight teeth, each tooth composed of two rows of cells, fenestrate and usually completely separated at the base, strongly vertically striate-reticulate, some striations forked-like in shape. At the base of the teeth, some striations are horizontally orientated, poorly developed or absent, particularly on the cell wall that is rupturing in the separation of the vertical rows of the cells that form each tooth.

Keywords

Brazil, Bryophyta, fenestrate, Panama, peristome, reticulate

Introduction

Octoblepharum Hedw. is a widely-distributed moss genus that is found in tropical and subtropical regions. The genus was erected by J. Hedwig in his Species Muscorum Frondosorum in 1801. It was described to include plants with single peristomes of eight teeth, capsules with an apophysis and autoicous gametangia (flos masculus femineo) (Hedwig 1801). The name derives from the Greek words okto (οξτο: eight) and blepharis (βλεπηαρισ: an eyelash), based on the eight peristome teeth of the type species, O. albidum Hedw., which was described from material collected by Swartz in Jamaica (Hedwig 1801). Of the 20 species recognised worldwide (see Salazar Allen and Chantanaorrapint 2018, for details on species distribution), eleven are reported for the Neotropics (Salazar Allen 1991, 1992, 1994). These are O. albidum, O. ampullaceum Mitt., O. costatum H.A. Crum, O. cocuiense Mitt., O. cylindricum Schimp. ex Mont., O. erectifolium Mitt., O. leucobryoides O. Yano, O. pulvinatum (Dozy & Molk.) Mitt., O. rhaphidostegium Müll. Hal., O. stramineum Mitt. and O. tatei (Williams) E.B. Bartram. The report of O. africanum from Brazil (Yano 1992) is doubtful as illustrations of the peristome do not correspond to the peristome described in the protologue (Cardot 1899), nor those observed by the senior author at (H). The status of O. costatum is also doubtful: based on the description by Crum (1983), Frahm (1994) suggested that this species could be a synonym of O. cocuiense.

Our taxonomic revision of numerous (over 300) neotropical specimens, thought to represent the pantropical O. albidum, showed very similar gametophytic morphology, but significantly distinct peristome structure and ornamentation. After reviewing specimens of O. albidum from the Province of Coclé in Panama, Brazil and other countries and relevant literature (Cardot 1899; Yano 1992; Salazar Allen 1992, 1994; Salazar Allen and Tan 2010; Salazar Allen and Chantanaorrapint 2018), we concluded that the examined material from the said specimens from Coclé in Panama and Brazil represent an undescribed species, which we formally describe below as Octoblepharum peristomiruptum.

Materials and methods

From 2017–2019, we conducted morphological studies of fresh specimens from Panama and herbarium specimens from South America. Photographs of specimens in the field were taken with a LG K10, 2017 cell phone. Measurements of the morphological characters were made using a Leica-MZ6 stereomicroscope and an Olympus DPX50 light microscope. Microphotographs were obtained with an Olympus DP25 digital camera mounted on the latter microscope. Scanning electron micrographs (SEM) were made of samples from Panama and Brazil, following a modification of the methodology used by Salazar Allen (1993). Samples were viewed at different magnifications using a Zeiss Model Evo 40 vp SEM, with a backscattered electron detector and an acceleration voltage of 25 Kv, setting at the Smithsonian Tropical Research Institute (STRI), Panama. Digitised SEM images were post-processed and assembled in multipart figures using Adobe Photoshop.

Taxonomic treatment

Octoblepharum peristomiruptum Salazar Allen & Gudiño, sp. nov.

Figs 1, 2, 3, 4

Diagnosis

Octoblepharum peristomiruptum is distinguished by its reddish to dark-purple coloured leaf bases, containing purple-coloured chlorocysts, with hyaline lamina 8–14 cells wide, unequally wide on each side of the costa, with purple cell walls, the exserted cylindrical capsule with long rostrate operculum and eight strongly vertically striate-reticulate teeth with the two rows of cells forming each tooth frequently separated at base.

Figure 1. 

Octoblepharum peristomiruptum Salazar Allen & Gudiño. Photographs A habit in its natural environment B enlarged group of plants. Microphotographs C cross section of stem with young leaf (lf) D apex of leaf E chlorocysts near apex of leaf F chlorocysts at base of leaf (note the strong reddish-purple colouration) G enlarged hyalocysts on leaf border H rhizoids originating from border of leaf chlorocysts I rhizoids at apex of leaf. All from Gudiño 3519 (PMA).

Type

Panama. Coclé: Distrito de Penonomé, above Chiguirí Arriba, Mariposario Cerro La Vieja, 8°39.88'N, 80°12.07'W, 360 m alt., 1 Jan 2019, J.A. Gudiño L. 3519 (holotype: PMA!; isotypes H!, NY!).

Figure 2. 

Octoblepharum peristomiruptum Salazar Allen & Gudiño. Microphotographs A leaf, hyaline lamina B–D cross sections of leaf B near apex C at mid-leaf D at base E androecium F–I male bracts J antheridium and paraphysis K paraphyses of gynoecium A taken from Kulhmann 1621 (NY), B–K taken from Gudiño 3519 (PMA).

Description

Plants (2.3–)3.5–5.0 cm tall. Stems erect, lacking a central strand of differentiated cells and thick-walled border cells, slightly tomentose at base, branching monopodial (pseudodichotomous), innovations arising early, during development of sporophyte. Rhizoids dark orange-red, arising from stem and leaves. Leaves ligulate, dentate in distal half, smooth at base, erect to slightly reflexed in upper third, (4.0–)5.5–6.7(–8.0) mm long, (0.4–)0.5–1.2 mm wide at base, including hyaline lamina; apex apiculate, ending in an elongate cell flanked by 2 hexagonal cells; margins of leaf slightly undulate due to swollen hyalocysts, these single or in groups of 2–3 cells. Limbidium extending from leaf apex to mid-leaf, 2(–3) cells wide, thinner at base. Hyaline lamina adpressed to stem, unistratose, composed of thin-walled pitted hyalocysts, the hyalocysts long and hexagonal at apex, hexagonal to pentagonal at mid-lamina next to costa and rectangular, quadrate and short pentagonal basally. Costa in cross-section composed of ventral and dorsal porose hyalocysts supporting a unistratose, median network of small, thick-walled chlorocysts, in cross-section chlorocysts forming an irregularly zig-zag row, quadrate to triangular at base and triangular to tear-shaped above; the chlorocysts at leaf base, below hyaline lamina, surrounded by one layer of porose hyalocysts ventrally and three layers dorsally, at hyaline lamina hyalocysts in 1–2 rows ventrally and 4 rows dorsally, at mid-leaf in 3 layers ventrally and 3–4 layers dorsally, near apex 2 layers ventrally and two dorsally. Autoicous, perigonia axillary in short branches below the archegonia, antheridia surrounded by 5–7 small, mostly hyaline leaves (in some, only the central area of the leaf with chlorocysts), paraphyses 4–5 cells long with 1–2 brown basal cells, perichaetia terminal, archegonia with paraphyses to 10 cells long and with 1–2 short brown basal cells. Setae dark orange-red, smooth, sinistrorse, 4–5 mm long. Capsules dark red when mature, cylindrical (1.3–)1.6–2.0 mm long, the exothecial cells at mouth of capsule quadrate, dark red with slightly thickened transversal walls, at mid-capsule rectangular and quadrate with dark orange, thick longitudinal walls and thin transversal walls, (56–)80–92(–115) µm, becoming shorter towards mouth of capsule (26–)32–44 µm, phaneroporous stomata present at base of capsule. Prostome present. Peristome of eight elongate triangular teeth, inserted in mouth of capsule, each tooth composed of 2 rows of cells, basally fenestrate, strongly striate vertically, sometimes striations horizontally orientated at base and fading or absent in areas where separation of the rows of cells composing the tooth occurs. Operculum conic, long – rostrate, slightly curved. Calyptra cucullate, apex dark red, beige below. Spores brown, spheroid, densely gemmate, 14–16 µm.

Figure 3. 

Octoblepharum peristomiruptum Salazar Allen & Gudiño. Microphotographs A four peristome teeth B dorsal view of peristome teeth with the two vertical rows of cells composing the teeth separating at base C two teeth with early and late separation of the two rows of cells D border and upper exothecial cells of capsule. A, B, D taken from Occhioni 668 (H), C taken from Gudiño 3519 (PMA).

Additional specimens examined (paratypes)

Brazil. Pará: Belem, Museu Goeldi, 29 Aug 1927, P. Occhioni 668 (H), Belem, 13 Aug 1923, J.G. Kulmann s.n. (HBR-H), 1½ hr. upstream from Lageira airstrip, on Rio Maicuru, 0°55'S, 54°26'W, 243.84 m alt., 23 Jul 1981, J.J. Strudwick & G.L. Sobel 3443 (NY); Matto Grosso: Pacca Nova, affl. do Mamoré, 23 Sept 1923, J.G. Kulmann 516 (HBR-H).

Habitat, distribution and phenology

Octoblepharum peristomiruptum was found on the cortex of a shrub, at 2 m above soil level in a private butterfly garden in the Coclé Province, Panama. The site is on the edge of the road. The climate in this area is characterised by average temperatures ranging from 23–30 °C (http://www.accuweather.com, accessed Jan 2020). In Brazil, the plant was found in three sites, on a living tree trunk in the “Museu Goeldi” reserve in Belem (Pará), on the trunk of a palm tree in a forested area in Matto Grosso and on a living tree trunk in a seasonally-flooded (varzea) forest. It is distributed in southern and northern Brazil and Central America (Panama). Plants with sporophytes were collected in Panama in January and, in Brazil in July, August and September.

Eponymy

The species name refers to the character of the peristome teeth that rupture at base separating the two rows of cells that compose each tooth.

Conservation status

The new species has been found in Coclé Province, Panama in a private conservation site and in the State of Pará, Brazil, on trees in the garden of the “Museu Goeldi” that is considered a reserve site. The conservation status of the other collection sites in Brazil is unknown. It is most probable that the species also occurs in other Central and South American countries. Given the limited knowledge of the current state of the sites where collections were made, the conservation status cannot be properly assessed. Thus, this new species is temporarily considered Data Deficient (DD).

Figure 4. 

Octoblepharum peristomiruptum Salazar Allen & Gudiño. Scanning electron microscopy micrographs A sporophyte B peristome teeth dorsal view C close-up of rupturing wall D ventral view of two teeth E ventral view at base of two teeth F spore A–C, E, F taken from Gudiño 3519 (PMA), D taken from Strudwick & Sobel 3443 (NY).

Discussion

Octoblepharum peristomiruptum is characterised by its tall habit, reddish stems, leaves with a strong dark reddish-purple colour at the base, exserted setae, cylindrical capsules and eight vertically striate-reticulate peristome teeth, each with two rows of cells separating at the base. Amongst other Octoblepharum species with eight peristome teeth, some populations of O. albidum have slightly pink-coloured leaves, 4–6(–8) mm long, but with the peristome mostly smooth or faintly striate, unlike O. peristomiruptum. Furthermore, Salazar Allen (1992) reported another O. albidum specimen (Salazar # 6588) with red-purple leaves and strongly striate teeth with pronounced trabeculae, but this latter character is not present in O. peristomiruptum. Peristome teeth in most populations of O. albidum studied are solid, although sometimes they may have perforations at the base, as reported by Yano (1992). These perforations, however, are not as pronounced as those of O. peristomiruptum. Finally, the recent segregation of a new Octoblepharum species, previously included in O. albidum by Salazar Allen and Chantanaorrapint (2018), indicates that the specimen recorded in Salazar Allen (1992) needs further examination to ascertain its proper taxonomic status. Octoblepharum albidum, as currently construed, might comprise a complex of cryptic species sharing similar gametophytic morphology, but with distinctive peristome structures and ornamentation (Salazar Allen and Chantanaorrapint 2018).

Other species of Octoblepharum with eight peristome teeth are O. ampullaceum, O. benitotanii Salazar Allen & Chantanaorr., O. cylindricum, O. erectifolium, O pocsii Magill & B.H. Allen and O. rhaphidostegium. Compared to O. peristomiruptum, the leaves of O. ampullaceum are longer (7–10 mm), tumid and the peristome is composed of eight pairs of slender, smooth teeth (Yano 1992). Octoblepharum benitotanii, an Asiatic species, has shorter leaves (4.5–5.5 mm) with a prominent apiculus and the peristome has teeth with strongly foveolate-reticulate ornamentation on both surfaces and faint trabeculae (Salazar Allen and Chantanaorrapint 2018). Octoblepharum cylindricum has longer leaves (6–12 mm) with a light pink colouration at the base, the sporophyte has a long seta (10–18 mm) and the peristome teeth have a thickened mid-line and prominent trabeculae (Salazar Allen 1994). Octoblepharum erectifolium gametophytes have longer (15–25 mm), fragile leaves (Yano 1992) and the sporophyte has a long seta (to 16 mm) and eight elongate peristome teeth with pronounced trabeculae and reticulate ornamentation (Salazar Allen 1994). Octoblepharum pocsii is an African species with longer leaves (10–13 mm) and a peristome of short, fragile and smooth teeth (Magill and Allen 2013). Octoblepharum rhaphidostegium is dioicous, rather than monoicous as in O. peristomiruptum and the other species discussed above and it has a peristome with faint vertical striations, prominent trabeculae and a thickened mid-line (Müller 1895).

Acknowledgements

The authors are grateful to STRI for research funds to Salazar Allen and to the following herbaria for loans of Octoblepharum: F, G, H, JE and NY. One of us (José Gudiño) took photos of the habit and prepared samples for SEM. Our deepest gratitude goes to J. Ceballos (STRISEM technician) for SEM micrographs and to I. A. Valdespino, A. Aiello and L.L. Forrest for revision of the manuscript and the English. Finally, we acknowledge support by the STRI Scientific Permit Office with revision and submission of the permit forms and to the Ministry of the Environment of Panama for collecting permits.

References

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