Stellarangia namibensis Kärnefelt) Frödén, Arup & Søchting was originally described by (Kärnefelt (1988)Kärnefelt I. 1988. Two closely related species of Caloplaca (Teloschistaceae, Lichenes) from the Namib Desert. Bothalia 18: 51-56. as Caloplaca namibensis Karnef. based on his own material, collected in Namibia, and that of Welwitsch from southern Angola (Benguela). According to Kärnefelt (1988)Kärnefelt I. 1988. Two closely related species of Caloplaca (Teloschistaceae, Lichenes) from the Namib Desert. Bothalia 18: 51-56., C. namibiensis is close to Caloplaca elegantissima (Nyl.) Zahlbr., and differs from C. namibensis mainly by the presence of isidia, which are absent in C. elegantissima, as well as by the lobe width, which is narrower in C. namibensis (0.2-0.5 mm) than in C. elegantissima (0.5-1.8 mm). The author also pointed out to the difference in the separation between lobes and the thickness of the epinecral layer, observing a lower distance between lobes and a thinner epinecral layer in C. namibensis. The other species in the group, C. testudinea, is also isidiate, but in this case lobes are usually much shorter to sometimes absent (Wirth & al. 2005Wirth V., Kärnefelt I., Thell A. & Arup U. 2005. Caloplaca testudinea V. Wirth & Kärnefelt sp. nov. and C. rubelliana (Ach.) Lojka, new to southern Africa. Mycological Progress 4: 299-302. ).
In the most recent classification of the family Teloschistaceae, Arup & al. (2013)Arup U., Søchting U. & Frödén P. 2013. A new taxonomy of the family Teloschistaceae. Nordic Journal of Botany 31: 16-83. proposed the monophyletic genus Stellarangia to accommodate three species occurring in the deserts of south-western Africa and developing “beautiful long lobes”: Stellarangia elegantissima (Nyl.) Frödén, Arup & Søchting, S. namibensis and S. testudinea (V.Wirth & Kärnefelt) Frödén, Arup & Søchting.
The Atlantic Sahara specimens examined in this study are sterile, covered by isidia, mostly simple and scattered, but sometimes becoming clustered towards the centre of the thallus, and then appearing coralloid. Lobes are narrow, never exceeding 0.5 mm in width, mostly closely adpressed but occasionally more separated, and even disjunct. Such variation appears to be dependent on thallus developmental stage and/or determined by substrate microtopography. The surface is orange (K+ purple) to salmon pigmented due to a strongly developed white epinecral layer, which can leave the centre of the thallus virtually white (Fig. 1b). The epinecral layer is absent at the lobe tips but can be up to 50 µm thick towards the centre. Cortex is as described by Kärnefelt (1988)Kärnefelt I. 1988. Two closely related species of Caloplaca (Teloschistaceae, Lichenes) from the Namib Desert. Bothalia 18: 51-56., i.e. composed of strongly gelatinized hyphae that are mostly hyaline, with an orange-yellowish thin layer above, but is sometimes reduced to the pigmented layer directly contacting, and partially involving, the characteristic algal clusters. Algal clusters are frequently separated by hyphae stacks extending downwards from the cortex.
These specimens were found on January 5, 2016, about 6 km north of Sabkhat Fares (22.579995N, 16.35907W). They were growing on white quartz pebbles embedded in the sandy and gravelly coastal cliffs of the Hamada Plateau (Fig. 1a), which is in agreement with Kärnefelt’s description of the ecology of Caloplaca namibensis in the Namib Desert (Wirth 2010Wirth V. 2010. Lichens of the Namib Desert: a guide to their identification. Klaus Hess Publishers, Windhoek.; de los Ríos & al. 2022de los Ríos A., Garrido-Benavent I., Limóna A., Cason E.D., Maggs-Kölling G., Cowan D. & Valverde A. 2022. Novel lichen-dominated hypolithic communities in the Namib Desert. Microbial Ecology 83: 1036-1048. ). The climate is hot (average daily maximum temperature of 23°C) and arid, with scarce amounts of episodic rainfall (average less than 20 mm annual rainfall). Fogs blown in from the Atlantic are common, which condense and supply the majority of moisture needed for lichens to grow. The whole area is influenced by the cold Canary Current which flows southwards from the northern Atlantic Ocean along the north-western coast of Africa.
Our proposed explanation for the occurrence of Stellarangia namibensis in this particular locality of north-western Africa is a combination of the favourable environmental conditions of the Atlantic Coastal Desert, similar to the conditions found in the Namib Desert, and the suitable substrate for its growth provided by the stable quartz pebble field, which seems to be uncommon in this region, contrary to what happens in the Namib (Schieferstein & Loris 1992Schieferstein B., Loris K. 1992. Ecological investigations on lichen fields of the Central Namib. Vegetatio 98: 113-128. ; de los Ríos & al. 2022de los Ríos A., Garrido-Benavent I., Limóna A., Cason E.D., Maggs-Kölling G., Cowan D. & Valverde A. 2022. Novel lichen-dominated hypolithic communities in the Namib Desert. Microbial Ecology 83: 1036-1048. ).
The number of accompanying species in the locality was remarkably low. The most conspicuous was Elenkiniana gloriae (Llimona & Werner) S.Y.Kondr., Kärnefelt, Elix, A. Thell, Jung Kim, A.S.Kondr. & Hur., but Buellia vandenboomii Giralt & Brand, Diploicia canescens (Dicks.) A.Massal., Diplotomma alboatrum (Hoffm.) Flot., Niebla bourgaeana (Mont. ex Nyl.) Rundel & Bowler (salazinic acid chemotype) and Ramalina maciformis (Delise) Bory, were also present. Buellia vandenboomii is a new report for continental Africa. We searched for S. namibensis in other localities along the coast of the Atlantic Sahara, from Cape Bojador down to the border with Mauritania and no further occurrences were noted. Future survey efforts focused on finding suitable habitats for S. namibensis along the north-western African coast might well include this and other unexpected lichen taxa.
Specimens examined and comments
⌅Stellarangia namibensis (Kärnefelt) Frödén, Arup & Søchting.-MOROCCO. Dakhla-Oued Ed-Dahab: Oued Ed-Dahab Province, N of Sabkhat Fares, 22.579995N, 16.35907W, on quartz pebbles, 5 Jan. 2016, J.C. Brito [PO-L9756]; ibid., 4 Apr. 2017, J. Marques [PO-L9759, PO-L9760, PO-L9761, PO-L9762].
Elenkiniana gloriae (Llimona & Werner) S.Y.Kondr., Kärnefelt, Elix, A.Thell, Jung Kim, A.S.Kondr. & Hur.-MOROCCO. Dakhla-Oued Ed-Dahab: Oued Ed-Dahab Province, N of Sabkhat Fares, 22.579995N, 16.35907W, on quartz pebbles, 5 Jan. 2016, J.C. Brito [PO-L9757]; ibid., 4 Apr. 2017, J. Marques [PO-L9765, PO-L9766].
A presumed synonym of Elenkiniana gomerana (J.Steiner) S.Y.Kondr., Kärnefelt, Elix, A. Thell, Jung Kim, A.S.Kondr. & Hur (Gaya & al. 2003Gaya E., Lutzoni F., Zoller S. & Navarro-Rosinés P. 2003. Phylogenetic study of Fulgensia and allied Caloplaca and Xanthoria species (Teloschistaceae, lichen-forming Ascomycota). American Journal of Botany 90: 1095-1103.) characterised by the thick effigurate thallus with numerous pseudocyphellae (Kondratyuk & al. 2014Kondratyuk S.Y., Jeong M.-H., Yu N.-N., Kärnefelt I., Thell A., Elix J., Kondratyuk A.S. & Hur, J.-S. 2014. A revised taxonomy for the subfamily Caloplacoideae (Teloschistaceae, Ascomycota) based on molecular phylogeny. Acta Botanica Hungarica 56: 93-123.). Previously known from southern Spain (Andalucía), the Canary Islands and Morocco (Llimona & Werner 1975Llimona X., Werner R.G. 1975. Quelques lichens nouveau ou interessants de la Sierra de Gata (Almeria, SE de l’Espagne). Acta Phytotaxonomica Barcinonensia 16: 1-32.). Our records extend the known distribution of the species in North Africa towards the south in the Atlantic Coastal Desert.
Buellia vandenboomii Giralt & M.Brand.-MOROCCO. Dakhla-Oued Ed-Dahab: Oued Ed-Dahab Province, N of Sabkhat Fares, 22.579995N, 16.35907W, on Diplotomma alboatrum (Hoffm.) Flot and directly on calcareous stones, 4 Apr. 2017, J. Marques [PO-L9764b].
Previously known only from the type locality in the Canary Islands, this lichen is distinguished from other xanthone-containing species of the genus Buellia (Giralt & al. 2009Giralt M., Paz-Bermúdez G. & Elix J.A. 2009. The saxicolous, xanthone-containing species of the genus Buellia s.l. (Physciaceace, Ascomycota) in the Iberian Peninsula. Nova Hedwigia 89: 321-334. ) by the small, smooth Physconia-type ascospores, the presence of an aeruginose, N+ red-violet pigment in the epihymenium, and well developed thick, areolate, yellow thallus lacking norstictic acid. Our specimen differs from the original description in thallus colour (white to very pale yellow) and habitat (on calcareous stones instead of volcanic rocks).
Diploicia canescens (Dicks.) A.Massal.-MOROCCO. Dakhla-Oued Ed-Dahab: Oued Ed-Dahab Province, N of Sabkhat Fares, 22.579995N, 16.35907W on calcareous stones, 5 Jan. 2016, J.C. Brito [PO-L9758a].
Diplotomma alboatrum (Hoffm.) Flot.-MOROCCO. Dakhla-Oued Ed-Dahab: Oued Ed-Dahab Province, N of Sabkhat Fares, 22.579995N, 16.35907W, on calcareous stones, 4 Apr. 2017, J. Marques [PO-L9764a].
Niebla bourgaeana (Mont. ex Nyl.) Rundel & Bowler.-MOROCCO. Dakhla-Oued Ed-Dahab: Oued Ed-Dahab Province, N of Sabkhat Fares, 22.579995N, 16.35907W, on calcareous stones, 5 Jan. 2016, J.C. Brito [PO-L9758b].
A Mediterranean-African species characterized by the cuneate, rigid, strongly reticulately ridged laciniae and abundant apothecia, that are mostly laminal (Krog & Østhagen 1980Krog H., Østhagen H. 1980. The genus Ramalina in the Canary Islands. Norwegian Journal of Botany 27: 255-296., Aptroot & Schumm 2008Aptroot A., Schumm F. 2008. Key to Ramalina species known from Atlantic islands, with two new species from the Azores. Sauteria 15: 21-57.).
Ramalina maciformis (Delile) Bory.-MOROCCO. Dakhla-Oued Ed-Dahab: Oued Ed-Dahab Province, N of Sabkhat Fares, 22.579995N, 16.35907W, on quartz pebbles, 4 Apr. 2017, J. Marques [PO-L9763].
An African-Arabian species distinguished from the previous one by the presence of an irregular network of large cracks exposing the medullary layer, from which granular soredia originate (Krog & Østhagen 1980Krog H., Østhagen H. 1980. The genus Ramalina in the Canary Islands. Norwegian Journal of Botany 27: 255-296., Aptroot & Schumm 2008Aptroot A., Schumm F. 2008. Key to Ramalina species known from Atlantic islands, with two new species from the Azores. Sauteria 15: 21-57.).