First Checklist of Lichens and Lichenicolous Fungi from Mauritius, with Phylogenetic Analyses and Descriptions of New Taxa

First Checklist of Lichens and Lichenicolous Fungi from Mauritius, with Phylogenetic Analyses and Descriptions of New Taxa

Plant and Fungal Systematics 65(1): 13–75, 2020 ISSN 2544-7459 (print) DOI: https://doi.org/10.35535/pfsyst-2020-0003 ISSN 2657-5000 (online) First checklist of lichens and lichenicolous fungi from Mauritius, with phylogenetic analyses and descriptions of new taxa Paul Diederich1* & Damien Ertz2,3 Abstract. A first checklist of the lichens and lichenicolous fungi from the Republic of Article info Mauritius is presented. It is based on older literature reports and on collections made by the Received: 29 Sept. 2019 authors, mainly in 2016, from the isles of Mauritius and Rodrigues. A total of 216 species Revision received: 11 Mar. 2020 are accepted, either as relevant specimens have recently been critically studied or revised Accepted: 16 Mar. 2020 by lichen taxonomists, or as we have collected and identified such material ourselves. Published: 2 Jun. 2020 A further 226 taxa have been reported from Mauritius but are not accepted here, either Associate Editor as no relevant herbarium material has recently been examined, or as previous records are Nicolas Magain dubious or erroneous; 111 taxa have been newly described from Mauritius in the past, plus 12 of which the Mauritian origin is dubious. Here we report 56 taxa as new for the island of Mauritius, and we describe two new genera (Baidera, Serusiauxia) and eight new species (Baidera mauritiana, Biatoropsis millanesiana, Chapsa alletii, Collemopsidium mauritiae, Nyungwea pyneei, Porina florensii, Pyrenula muriciliata, Serusiauxia inexpectata). Two new combinations are proposed: Loekoesia apostatica (≡ Lecanora apostatica) and Sticta flavireagens (≡ Stictina flavireagens). Phylogenetic analyses are presented for species of Arthoniales, Biatoropsis, Porinaceae, Pyrenulaceae and Teloschistales. Key words: Arthoniales, Biatoropsis, Indian Ocean, Porinaceae, Pyrenulaceae, Rodrigues, Teloschistales Introduction The Republic of Mauritius lies in the southwestern Indian with the more humid upper elevation, which receives Ocean about 900 km east of Madagascar and about the highest amount of rainfall. Fog is abundant at the 2000 km off the southeast coast of the African continent. upper altitudes and provides the optimum climate for the It consists of two main volcanic islands belonging to the development of rich macrolichen communities (Figs 1–2). Mascarene Archipelago: Mauritius, with a land area of The Mascarene Islands harbour a very rich and diverse 1865 km² (highest point Piton de la Petite Rivière Noire, angiosperm flora, with an estimated ~960 native species, 828 m); and Rodrigues, which is the smallest (109 km²; about 75% of them considered to be endemic to the archi- highest point Mt Limon, 398 m) and most isolated of the pelago (Thébaud et al. 2009). The level of island ende- Mascarene Islands, being located about 574 km east of mism is also high, being 39.5% in Mauritius (273 single Mauritius. Basaltic lava is the main type of rock on both island endemics of the 691 native species) and 31.1% in islands, but Rodrigues also has areas of limestone made Rodrigues (47 single-island endemics of the 150 native of consolidated coral sands. Mauritius and Rodrigues are species) (Baider et al. 2010). The archipelago is even the two oldest main islands of the Mascarenes, having part of the world’s most important biodiversity hotspots been available for colonization by diverse biota for 8–15 (Myers et al. 2000). The pristine fauna and flora of the million years (Thébaud et al. 2009). The coastal areas Mascarenes have been decimated since humans arrived of both islands have a dry tropical climate contrasting in 1598. The dodo (Raphus cucullatus), a flightless bird belonging to the Columbidae and endemic to Mauritius, is the emblematic representative of them (Cheke & Hume 1 Musée national d’histoire naturelle, 25 rue Munster, L-2160 Luxem- bourg, Luxembourg 2008). Although native vegetation remains, all the pris- 2 Meise Botanic Garden, Department of Research, Nieuwelaan 38, tine forest covering Rodrigues has been destroyed, while B-1860 Meise, Belgium barely 2% of the original forest cover has been left in 3 Fédération Wallonie-Bruxelles, Service général de l’Enseignement Mauritius, mainly lowland rainforests and dense cloud non obligatoire et de la Recherche scientifique, rue A. Lavallée 1, B-1080 Bruxelles, Belgium forests at the highest elevation. They are concentrated * Corresponding author e-mail: [email protected] in Black River Gorges National Park in the southwest, © 2020 W. Szafer Institute of Botany, Polish Academy of Sciences. This is an Open Access article distributed under the terms of the Creative Commons Attribution License CC BY 4.0 (http://creativecommons.org/licenses/by/4.0/) 14 Plant and Fungal Systematics 65(1): 13–75, 2020 the Bambou Mountain Range in the southeast, and the Porina florensii and Pyrenula muriciliata are given as Moka–Port Louis Ranges in the northwest, with some (min.–)average minus standard deviation–average plus isolated mountains such as Corps de Garde, Le Morne standard deviation(–max.). Brabant, and several offshore islets. These forest remnants are often invaded by alien animals (e.g., deer, mongooses, Molecular techniques monkeys, pigs, rats) and plant species (e.g., Psidium cat- Well-preserved and freshly collected specimens were used tleianum, Ardisia crenata, Ligustrum robustum, Rubus for sequencing. A group of 4 to 6 soredia (Serusiauxia) alceifolius, Wikstroemia indica) (Thébaud et al. 2009, or tiny fragments of the hymenium or thallus (Baidera Virah-Sawmy et al. 2009), which have a strong negative mauritiana, Granulopyrenis sp., Loekoesia apostatica, impact on biodiversity. Considerable efforts are deployed Nyungwea pyneei, Porina florensii, Pyrenula quassiicola, for conservation management work to fight alien species Squamulea cf. squamosa) were used for direct PCR as and restore original forests. described in Ertz et al. (2015). For Biatoropsis millane- The lichen flora of Mauritius and Rodrigues is poorly siana, total DNA was extracted directly from the speci- known and has never been thoroughly revised. This paper mens examined (Table 1) using the Qiagen DNeasy Plant aims to provide a first checklist for the lichens and lichen- MiniKit according to the manufacturer’s instructions, but icolous fungi of Mauritius and Rodrigues, along with new using 50 μl of water in each of the last two steps of final records and descriptions of new species resulting from elution. our recent collecting trips. A targeted fragment of ~0.8 kb of the mitochondrial ribosomal RNA small subunit (mtSSU) was amplified for Material and methods Granulopyrenis, Loekoesia, Porina, Pyrenula and Squam- ulea using primers mrSSU1 and mrSSU3R (Zoller et al. Preparation of the checklist and morphological 1999), and a fragment of ~1 kb of the RPB2 protein-cod- examination ing gene was amplified forBaidera and Nyungwea using primers fRPB2-7cF and fRPB2-11aR (Liu et al. 1999). The checklist includes both data found in the literature Amplification reactions were prepared for a 50 µl final and new results based on our collections. The entire liter- volume containing the lichen material as explained in Ertz ature for Mauritius has been checked, and all previously et al. (2018b). The yield of the PCRs was verified by run- published reports of Mauritian lichens have been included ning the products on a 1% agarose gel using ethidium bro- in the checklist. Species printed in bold are accepted; mide. Both strands were sequenced by Macrogen® using these usually represent species either recently studied amplification primers. Sequence fragments were assem- and published by taxonomists or examined by us. Other bled with Sequencher v. 5.3 (Gene Codes Corporation, species are considered dubious, especially those from the Ann Arbor, Michigan). For Biatoropsis millanesiana, we older literature, as no specimens exist or as they have amplified nuc rDNA internal transcribed spacer 1 (ITS1), never been critically revised. We have not examined most 5.8S, internal transcribed spacer 2 (ITS2) and a fragment historical specimens, except for those indicated by an of ~1000 bp in the rDNA 28S region with primers ITS1F exclamation mark (!). Specimens we collected, mainly in (Gardes & Bruns 1993), BasidLSU3-3 (Millanes et al. 2016, are retained in MAU (Mauritius Herbarium), while 2011), BasidLSU1-3 (Millanes et al. 2011), BasidLSU1-5 duplicates are kept in BR (Damien Ertz) and in the private (Millanes et al. 2011), BasidLSU13-5 (Millanes et al. herbarium of P. Diederich. A few additional specimens 2011) and LR5 (Vilgalys & Hester 1990). PCR amplifi- from BM and MAU have been studied. cations were performed using Illustra™ Hot Start PCR Hand-made sections of ascomata and thalli were beads according to the manufacturer’s instructions, with studied in water, 5% KOH (K), Lugol’s reagent (1% I ) 2 the primer combinations and settings described in Millanes without (I) or with KOH pre-treatment (K/I), lactophe- et al. (2011). Sequencing followed Millanes et al. (2016). nol-cotton blue (LCB), Congo Red or phloxine B. Macro- scopic photographs were made using a Canon 40D camera Taxon selection and phylogenetic analyses with a Canon MP-E 65 mm lens or a Nikon BD Plan 10× microscope objective, StackShot (Cognisys) and Helicon Ten new mtSSU sequences were obtained for this study: Focus (HeliconSoft) for increasing the depth of field; one for Granulopyrenis (MN989203 for Ertz 21425), or with a Keyence VHX-5000 digital microscope and one for Loekoesia apostatica (MN989204 for Diederich a VH-Z20R/W/T lens (Baidera, Nyungwea, Serusiauxia). 18518), two for Porina florensii (MN989205 for Died- Microscopic photographs were prepared using a Leica erich 18348, MN989206 for Diederich 18453), one for DMLB microscope with interference contrast, fitted with Pyrenula quassiicola (MN989207 for Ertz 21460), four a Leica EC3 camera; or an Olympus BX51 microscope for Serusiauxia inexpectata (MN989208 for Diederich with interference contrast, connected to an Olympus Color 17815, MN989209 for Diederich 18239, MN989210 for View I digital camera (Baidera, Nyungwea, Serusiauxia). Ertz 21490, MN989211 for Ertz 21496) and one for Squa- Chemical spot reactions are abbreviated as K (5% KOH), mulea cf.

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