Floristic Similarities between the Lichen Flora of Both Sides of the Drake Passage: A Biogeographical Approach
1
Faculty of Pharmacy, Section of Botany, Complutense University, Pl. de Ramón y Cajal, s/n, 28040 Madrid, Spain
2
Calle Navarro Villoslada 16, 3º dcha., Navarra, 31003 Pamplona, Spain
*
Author to whom correspondence should be addressed.
J. Fungi 2024, 10(1), 9; https://doi.org/10.3390/jof10010009
Submission received: 15 November 2023
/
Revised: 12 December 2023
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Accepted: 20 December 2023
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Published: 22 December 2023
(This article belongs to the Special Issue Lichen Forming Fungi—in Honour of Prof. Ana Rosa Burgaz)
Abstract
:This paper analyses the lichen flora of Navarino Island (Tierra del Fuego, Cape Horn Region, Chile), identifying species shared with the South Shetland Islands (Antarctic Peninsula). In this common flora, species are grouped by their biogeographic origin (Antarctic–subantarctic endemic, austral, bipolar, and cosmopolitan), their habitat on Navarino Island (coastal, forest, and alpine), their morphotype (crustaceous, foliaceous, fruticulose, and cladonioid), and the substrate from which they were collected (epiphytic, terricolous and humicolous, and saxicolous). A total of 124 species have been recognised as common on both sides of the Drake Passage, predominantly bipolar, crustaceous, and saxicolous species, and with an alpine distribution on Navarino Island. The most interesting fact is that more than 30% of the flora is shared between the southern tip of South America and the western Antarctic Peninsula, which is an indication of the existence of a meridian flow of propagules capable of crossing the Antarctic polar front.
1. Introduction
The Antarctic flora is usually viewed as being particularly isolated and unique, with special attention given to its high proportion of endemic species in both mosses and lichens [1,2,3]. However, when considering the overall diversity of Antarctica, it is clear that this region is neither isolated nor depauperate [4]. Although the Antarctic continent is far away from other land masses, the Antarctic Peninsula and adjacent islands are only 900 km away from the southern tip of South America, where high mountains, permanent snow cover, and glaciers provide an environment more similar to that of Antarctica than most of the subantarctic islands scattered across the south of the trans-hemispheric oceans. Both sides of the Beagle Channel are dominated by steep slopes, often over a thousand metres high, well above the tree line. An important part of this area, including Navarino Island, is protected and managed under the umbrella of the Cape Horn Biosphere Reserve [5].
Nevertheless, the powerful Antarctic Polar Front (APF) running just between Cape Horn and the Antarctic Peninsula is a major barrier to the latitudinal gradient of dispersal of plant propagules [2]. To what extent the APF has isolated the lichen flora of these two regions is still an open question with important implications in a global change scenario.
The Cape Horn region and the western Antarctic Peninsula share a climate dominated by westerly winds that bring moisture from the Pacific Ocean and reduce seasonal temperature variations. The main consequences are high annual precipitation rates, relatively mild winters, and cool summers. Very often, this precipitation occurs in the form of snow which only partially melts during the summer at altitudes of several hundred metres above sea level. A sharp tree line can only be observed at an altitude of about 450–500 m; above this altitude, pulvinar hemispherical shrubs are interspersed with alpine meadows and cryptograms, that become dominant from about 600 m high [5]. At this altitude, the mean annual air temperature is comparable to that measured at the Antarctic stations on the South Shetland Islands [6].
It is not surprising, therefore, to find a cryptogamic tundra in the Beagle Channel mountains that is physiognomically very analogous to that of the western Antarctic Peninsula. Something similar could be said of the coast, where both shingle beaches and cliffs support lichen communities that mirror those of the South Shetland Islands. On the other hand, both sides of the Drake Passage show an equivalent floristic richness of lichen flora which amounts to about 300–400 species in each of these regions. However, it remains an open question whether this is just a physiognomical affinity and how many species are actually shared between the two sites. The aim of this paper is to analyse the recently published lichen flora of Navarino Island [7], one of the largest and highest islands on the southern side of the Beagle Channel, to determine the degree of affinity with the West Antarctic region (more specifically, with the South Shetland Islands). Within the set of common species, we aim to quantify their distribution along the main altitudinal ranges present on Navarino Island, taking into account their morphology, substrate, habitat, and biogeographical origin.
2. Materials and Methods
2.1. Common Species between Navarino Island and the West Antarctic Region
We carried out a floristic analysis that benefits from several studies initiated by our group over 30 years ago in the West Antarctic Peninsula region [8,9,10] and on Navarino Island [7,11]. To identify lichen species shared between said regions, the Antarctic lichen flora [12] and the lichen flora of King George Island [13] were also examined. Nomenclature conforms almost entirely to that used on the website of the Consortium of Lichen Herbaria (CNALH) and the Global Biodiversity Information Facility (GBIF).
The set of common species between Navarino Island and maritime Antarctica has been divided into four biogeographical groups according to Sancho et al. 1999 [9], Oevstedal and Lewis Smith 2001 [12], Olech 2004 [13], and Soechting et al. 2004 [10]: Antarctic–subantarctic endemic, which includes the subantarctic islands and the Cape Horn region; austral, i.e., Southern Hemisphere distribution; bipolar, species distributed throughout both polar regions as well as in the high mountains of both hemispheres; and cosmopolitan, species with a broad distribution around the globe. Shared specimens have also been categorised according to a simplified version of the three main altitudinal belts of Navarino Island: coastal area, forest, and alpine region. The coastal habitat consists of trees close to the sea, pebble beaches, cliffs, and rocky intertidal zones; the forest (from around a hundred-meter distance from the shore up to about 500 m a.s.l.) includes both evergreen subantarctic Magellanic rainforests and deciduous forests; and the alpine or high Andean habitat (above 500 m a.s.l.) comprises low shrubs, cushion plants, and rocks scattered beyond the timberline. Each species of the Antarctic–Fuegian flora has been assigned to the substrate(s) on which it was found on Navarino Island. Lichens growing on trunks, branches, wood, and bark on trees were considered epiphytic, as were those found on the branches of cushion bog shrubs such as Bolax gummifera and Empetrum rubrum in the alpine region. Specimens growing on rocks were classified as saxicolous, while those that developed on soil, humus, grasses, mosses, liverworts, and/or other lichens were seen as terricolous. It should be noted that substrate type and habitat are not mutually exclusive as some species were found living on different substrates across more than one habitat. All possibilities were taken into consideration for our study.
2.2. Similarity Indexes
Similarity indexes (SIs) were calculated between the lichen flora from Navarino Island and that of the South Shetland Islands; for both, there was a substantial number of published lists from detailed surveys already available [7,9,10,11,12,13]. The SIs were calculated for the site pair as follows:
where nc is the number of species common between the sites and Σn1 and Σn2 are the total number of species at each site.
2.3. Distributional Pattern Analysis
To evaluate the relevance of distributional patterns on the species shared by maritime Antarctica and Navarino Island, we designed a contingency analysis in which species occurrence was calculated in accordance with biogeographical origin, habitat, and substrate type. Since the table generated was a three-way contingency table, a Cochran–Mantel–Haenszel test (CMH test) was used to determine whether there were any associations between variables. Before performing the test, the assumption of homogeneous odd ratios across the levels of each variable was checked using the Woolf test from the R package ‘vcd’ [14]. A post hoc analysis for the CMH test was carried out with the R package ‘rcompanion’ [15]. Additionally, an analysis of the two-way contingency tables was performed using Pearson’s chi-square test of independence for the tables built according to distribution and habitat on one hand and to habitat and substrate type on the other. For the two-way contingency table between distribution and substrate type, a G-test of independence was implemented using the R package ‘DescTools’ (version 0.99.30) [16]. The post hoc analysis was conducted as a pairwise test using the R package ‘rcompanion’ (version 4.1.0) [15]. p < 0.01 was considered statistically significant for all tests performed. Plots were created using the R package ‘ggplot2′ (version 3.4.4) [17].
3. Results
3.1. Common Species between Navarino Island and the West Antarctic Region and Similarity Indexes
Overall, 124 out of the 411 lichen species listed from Navarino Island are shared with the South Shetland Islands, which means that 30.2% can be considered Antarctic–Fuegian flora. Within this common flora, the dominant biogeographical group is the bipolar group (63 species), followed by the cosmopolitan group (23 species), the endemic group (21 species), and lastly, austral group (17 species). The alpine region of Navarino Island harbours 43.8% of the flora shared with Antarctica, while the forest represents only 23.8%. The remaining 32.5% of this common flora corresponds to the coastline (Table 1). Otherwise, the crustaceous morphotype is the most abundant, followed by foliaceous, cladonioid, and fruticose morphotypes (Table 2).
On the other hand, since the lichen flora of the South Shetland Islands accounts for 313 species (combining the floras of Livingston Island and King George Island), 39.6% of them are present on the southern tip of South America. If we extract from the 411 Navarino lichen species those that appear to be exclusively epiphytic—around 115—and those whose presence in Antarctica is highly improbable, we would be left with a pool rather similar to the floristic richness of maritime Antarctica. The degree of similarity would then be remarkable on both sides of the Drake Passage. The SI considering the whole Navarino lichen flora with respect to the South Shetland Islands is 0.343, and it is 0.407 if we discard the exclusively epiphytic species.
In the Antarctic–Fuegian flora, Cladonia and Rhizocarpon are the genera with the highest numbers of species. Interestingly, no species belonging to the important genus Buellia are shared between both sides of the Drake Passage. Nor, of course, are the more typical forest species of the genera Nephroma, Sticta, and Pseudocyphellaria. A few species, such as Poeltidea perusta and Rhizocarpon geographicum, are found across all habitats on Navarino Island. Most of the shared species show sexual reproduction, but asexual propagules (soredia, isidia, and thalloconidia) are also common.
3.2. Distributional Pattern Analysis
The three-way contingency table (Table 3) showed that the alpine habitat had a high proportion of terricolous species with bipolar distribution (28.6%; see Table 3 and Figure 1). The alpine saxicolous and epiphytic species with bipolar distribution were also present in higher proportions with respect to the other three biogeographical origins considered in our study (23.8 and 9.5%, respectively). In the coastal habitat, bipolar saxicolous species were predominant (25.0%). Saxicolous specimens with endemic and cosmopolitan distributions are also notoriously present (16.7 and 13.3%, respectively). In the forest habitat, bipolar terricolous species are the most abundant ones (23.3%), followed by cosmopolitan terricolous (18.6%) and bipolar saxicolous (14.0%) species.
Regarding substrate, saxicolous lichens were dominant for all biogeographical groups except for the cosmopolitan group, for which the terricolous lichens prevailed. Epiphytes represent the smallest group in all cases (Figure 2).
The Woolf test for the two-way contingency table showed homogeneous odds ratios across the levels of each variable with a p-value of 0.6, thus satisfying the assumptions needed to perform the CHM test. The latter indicated that habitat and substrate are dependent on one another at a given distribution level (p = 0.00009). This dependence occurred in particular at the cosmopolitan distribution level, as shown by the post hoc analysis (p = 0.004), which can be explained by the fact that there are barely any epiphytic lichens with a cosmopolitan distribution in the Antarctic–Fuegian flora. Furthermore, there are no saxicolous representatives within this biogeographical group in the forest habitat. Most of the cosmopolitan specimens are either saxicolous in coastal areas or terricolous in forests.
The G-test of independence performed for the two-way contingency table built according to distribution and substrate type presented no statistically significant differences across levels (p = 0.131). The chi-square tests carried out for the tables that took into account habitat and distribution and habitat and substrate type showed that only the latter had any statistically significant differences (p = 0.0001). This finding corroborated the result given by the CMH-test. The post hoc analysis indicated that the dependence found between these two variables was mainly due to the distinct proportion of saxicolous versus terricolous species throughout the habitats (p = 0.0001), particularly in the coast and forest; while saxicolous lichens are mainly found in coastal areas, terricolous ones prefer forests. Epiphytic specimens, however, are distributed in a more uniform way across the three ambient types (Table 4).
4. Discussion
Antarctica is the most isolated continent on Earth. The powerful Antarctic Polar Front (APF) is a significant barrier to both marine and terrestrial organisms. However, there is evidence that this barrier can be overcome [4]. This is clearly the case for the lichen flora on both sides of the Drake Passage. The proportion of lichen species from the South Shetland Islands that are also found on Navarino Island is roughly 40%, and the same is true for the flora of Navarino Island if we extract the approximately 115 exclusively epiphytic species from its more than 400 known species [7] (ca. 42%). The SI between Navarino Island and the South Shetland Islands is between 0.342 and 0.407 (depending on whether the epiphytic species are included or not, respectively). This is similar to the SI between the large islands of the Canadian Arctic Archipelago [18], amongst which there are no significant geographical barriers. Additionally, active genetic exchange in both north–south and south–north directions has been reported for some species from the genera Usnea and Mastodia [19,20,21].
Among the common species surpassing the APF, the bipolar biogeographical group stands out, accounting for 50.8% of the Antarctic–Fuegian flora (Table 1). Most of the species belonging to this group have their largest distribution in the vast Arctic and high mountain areas of the Northern Hemisphere, but in many cases, their centre of diversity is yet to be determined. The cosmopolitan group (18.6%) includes those species that are able to cross all geographical and climatic barriers to then grow on any part of our planet, including Antarctica. Both the bipolar and the cosmopolitan percentages are very similar to those reported by Ochyra et al. (2008) [22] for Antarctic mosses. The austral biogeographical group (13.7%) includes some species that may have originated on the old continent of Gondwana, as did many vascular plants [23,24] and bryophytes [25]. Finally, the Antarctic–subantarctic endemic group (16.9%) should be considered to be composed of pre-Pleistocene survivors of the ice ages that somehow found refuge in ice-free areas, mainly on rocky substrates in coastal regions or nunataks [23,26,27]. Interestingly, some cosmopolitan species, such as Collema tenax (Sw.) Ach. and Lecidea lapicida (Ach.) Ach., and bipolar species, such as Caloplaca tirolensis Zahlbr. and Dermatocarpon polyphyllizum (Nyl.) Blomb. & Forssell, that live on the South Shetland Islands are not found on Navarino Island, evidencing more complex colonisation processes than just a latitudinal gradient of dispersal.
The evidence of APF crossings is also a warning of the possible arrival of invasive species in a global warming scenario. Newly arrived terrestrial species have already been documented in maritime Antarctica, but no lichens have been documented so far [28]. However, natural dispersal events are no longer necessary to bring invasive species to Antarctica. It has been estimated that 40% of scientific visitors and 20% of tourists carry plant propagules from northern regions [29].
In terms of habitat distribution, it is not surprising that the highest number of species from Navarino Island shared with maritime Antarctica is found in the alpine habitat and that the lowest number is found in the forest habitat. It is more interesting to note that the coast has a relatively high percentage of affinities with Antarctica. This may be related to the very recent onset of forests in this region, dated to the middle Holocene, between 6000 and 5000 years before the present in Tierra del Fuego [30] and slightly earlier on Isla de los Estados [31]. The encroachment of the Nothofagus forest separated what must have been a continuous tundra from the sea to the peaks, similar to what is found in the ice-free areas of Antarctica today. In any case, this is a region of strong climatic oscillations driven by changes in latitude and the strength of westerly winds. Incidentally, the maximum glacial extent of the Holocene occurred only about 800 years ago, well before the Little Ice Age, probably as a result of a southward shift of these dominant winds [32]. Vegetation must adapt to these continuous environmental changes, using the altitudinal gradient as a buffer against the effects of climatic oscillations.
It is also understandable that the preferred substrates for this Antarctic–Fuegian flora are rocks, and that epiphytes are the least common species type. There is a considerable number of species growing on soil or mosses, all of which would be considered components of a cryptogamic tundra in the strict sense. Most of these species belong to the genus Cladonia which, by far, accounts for the largest number of species in this Antarctic–Fuegian flora. Our knowledge of this genus is particularly good thanks to a study carried out by Burgaz and Raggio in 2007 [11]. Further monographic work on key genera is likely to add new species to our catalogue of Navarino Island.
Regarding morphology, it is striking that very few species with a cyanobacterial photosymbiont are shared between the two sites. For example, the genus Placopsis, which is ubiquitous in the Southern Hemisphere, shows no common species on either side of the Drake Passage, while there are species such as P. perrugosa that are shared between South America and New Zealand [33] and two others that are restricted to Antarctica (P. antarctica and P. contortuplicata). The same can be said for some large green algae lichen genera, such as Buellia, that are present and abundant on both sides of the Drake Passage and yet have no shared species. This suggests that the barrier between Antarctica and the rest of the world could be ecological rather than geographical. The cold Antarctic summer, with average temperatures only slightly above freezing, may be the main limiting factor for the establishment and germination of propagules from the north. Some maritime Antarctic endemisms, such as Himantormia lugubris, show an extreme dependence on these cold and wet summer conditions [34]. In a warming scenario, these endemic species would be expected to decline in favour of other more widely distributed taxa [35]. Long-term studies at numerous sites on the Antarctic Peninsula and adjacent islands are essential to detect changes in floral composition that can only be hypothesised at this stage.
Author Contributions
Conceptualization, L.G.S. and J.E.; methodology, L.G.S. and N.B.-S.; formal analysis, N.B.-S.; investigation, L.G.S., A.A., J.E. and N.B.-S.; resources, L.G.S. and J.E.; data curation, L.G.S. and J.E.; writing—original draft preparation, L.G.S., A.A. and N.B.-S.; writing—review and editing, L.G.S., A.A. and J.E.; visualization, L.G.S. and A.A.; supervision, L.G.S.; project administration, L.G.S.; funding acquisition, L.G.S. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by the Spanish Ministry of Science via the project POLAR ROCKS (PID2019-105469RB-C21).
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Lichen samples used are deposited in the Pharmacy Herbarium MAF of the Complutense University of Madrid.
Acknowledgments
The authors thank the Pharmacy Herbarium MAF of the Complutense University of Madrid for providing herbarium specimens.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Convey, P.; Bowman, V.; Chown, S.L.; Francis, J.; Fraser, C.; Smellie, J.L.; Storey, B.; Terauds, A. Ice-Bound Antarctica: Biotic Consequences of the Shift from a Temperate to a Polar Climate. In Mountains, Climate and Biodiversity, 1st ed.; Hoorn, C., Perrigo, A., Antonelli, A., Eds.; John Wiley & Sons: Oxford, UK, 2018; pp. 355–373. ISBN 978-1-119-15987-2. [Google Scholar]
- Muñoz, J.; Felicisimo, A.M.; Cabezas, F.; Burgaz, A.R.; Martinez, I. Wind as a long-distance dispersal vehicle in the Southern Hemisphere. Science 2004, 304, 1144–1147. Available online: https://www.science.org/doi/10.1126/science.1095210 (accessed on 15 September 2023). [CrossRef] [PubMed]
- Terauds, A.; Chown, S.L.; Morgan, F.; Peat, H.J.; Watts, D.J.; Keys, H.; Convey, P.; Bergstrom, D.M. Conservation biogeography of the Antarctic. Divers. Distrib. 2012, 18, 726–741. [Google Scholar] [CrossRef]
- Chown, S.L.; Clarke, A.; Fraser, C.I.; Cary, S.C.; Moon, K.L.; McGeoch, M.A. The changing form of Antarctic biodiversity. Nature 2015, 522, 431–438. [Google Scholar] [CrossRef] [PubMed]
- Rozzi, R.; Massardo, F.; Anderson, C.; Berghoefer, A.; Mansilla, A.; Mansilla, M.; Plana, J.; Berghöfer, U.; Araya, P.; Barros, E.; et al. La Reserva de Biosfera Cabo de Hornos, 1st ed.; Ediciones Universidad de Magallanes: Punta Arenas, Chile, 2006. [Google Scholar]
- Laguna, C.; Pintado, A.; Green, A.; Blanquer, J.M.; Sancho, L.G. Distributional and ecophysiological study on the Antarctic lichens species pair Usnea antarctica/Usnea aurantiaco-atra. Pol. Biol. 2016, 39, 1183–1195. [Google Scholar] [CrossRef]
- Etayo, J.; Sancho, L.G.; Gómez-Bolea, A.; Søchting, U.; Aguirres, F.; Rozzi, R. Catalogue of lichens (and some related fungi) of Navarino Island, Cape Horn Biosphere Reserve, Chile. Ann. Inst. Patagon. 2021, 49, 1–110. [Google Scholar] [CrossRef]
- Sancho, L.G.; Kappen, L.; Schroeter, B. The lichen genus Umbilicaria on Livingston Island (South Shetland Islands, Antarctica). Antarct. Sci. 1992, 4, 189–196. [Google Scholar] [CrossRef]
- Sancho, L.G.; Schulz, F.; Schroeter, B.; Kappen, L. Bryophyte and lichen flora of South Bay (Livingston Island, South Shetland Islands, Antarctica). Nova Hedwig. 1999, 68, 301–337. [Google Scholar] [CrossRef]
- Søchting, U.; Øvstedal, D.O.; Sancho, L.G. The lichens of Hurd Peninsula, Livingston Island, South Shetlands, Antarctica. In Contributions to Lichenology. Festschrift in Honour of Hannes Hertel, 1st ed.; Döbbeler, P., Rambold, G., Eds.; Bibliotheca Lichenologica; J. Cramer in der Gebrüder Borntraeger: Berlin/Germany, Germany, 2004; Volume 88, pp. 607–658. ISBN 978-3-443-58067-4. [Google Scholar]
- Burgaz, A.R.; Raggio, J. The Cladoniaceae of Navarino Island (Prov. Antártica Chilena, Chile). Mycotaxon 2007, 99, 103–116. [Google Scholar]
- Øvstedal, D.O.; Lewis-Smith, R.I. Lichens of Antarctica and South Georgia. A Guide to their Identification and Ecology, 1st ed.; Cambridge University Press: Cambridge, UK, 2001; ISBN 978-0-521-66241-3. [Google Scholar]
- Olech, M. Lichens of King George Island, Antarctica, 1st ed.; Institute of Botany of Jagiellonian University: Kraków, Poland, 2004; ISBN 978-83-915161-7-1. [Google Scholar]
- Meyer, D.; Zeileis, A.; Hornik, K. vcd: Visualizing Categorical Data; R Package Version 1.4.8. 2020. Available online: https://CRAN.R-project.org/package=vcd (accessed on 16 October 2023).
- Mangiafico, S. Rcompanion: Functions to Support Extension Education Program Evaluation. R Package Version 4.1.0. 2022. Available online: https://CRAN.R-project.org/package=rcompanion (accessed on 16 October 2023).
- Signorell, A.; Aho, K.; Alfons, A.; Anderegg, N.; Aragon, T.; Arachchige, C.; Arppe, A.; Baddeley, A.; Barton, K.; Bolker, B.; et al. DescTools: Tools for descriptive statistics. R package Version 0.99.30. 2019. Available online: https://CRAN.R-project.org/package=DescTools (accessed on 16 October 2023).
- Wickham, H.; Chang, W.; Henry, L.; Pedersen, T.L.; Takahashi, K.; Wilke, C.; Woo, K.; Yutani, H.; Dunnington, D.; Posit, P.B.C. Ggplot2: Elegant Graphics for Data Analysis. R package Version 3.4.4. 2016. Available online: https://CRAN.R-project.org/package=ggplot2 (accessed on 16 October 2023).
- Türk, R.; Hogg, I.; Cox, E.R.; Sancho, L.G.; Williamson, S.N.; Bryan, V.; Green, T.G.A. The lichens of Cambridge Bay and vicinity. Nunavut, Victoria Island, Canada. University of Salzburg: Salzbug, Austria, 2024; to be submitted. [Google Scholar]
- Garrido-Benavent, I.; De los Ríos, A.; Pérez-Ortega, S. From Alaska to Antarctica: Species boundaries and genetic diversity of Prasiola (Trebouxiophyceae), a foliose chlorophyte associated with the bipolar lichen-forming fungus Mastodia tessellata. Mol. Phylogenet. Evol. 2016, 107, 117–131. [Google Scholar] [CrossRef]
- Garrido-Benavent, I.; Pérez-Ortega, S.; De los Ríos, A.; Fernández-Mendoza, F. Amphitropical variation of the algal partners of Pseudephebe (Parmeliaceae, lichenized fungi). Symbiosis 2020, 82, 35–48. [Google Scholar] [CrossRef]
- Zúñiga, C.; Leiva, D.; Ramírez-Fernández, L.; Carú, M.; Yahr, R.; Orlando, J. Phylogenetic Diversity of Peltigera cyanolichens and Their Photobionts in Southern Chile and Antarctica. Microbes Environ. 2015, 30, 172–179. [Google Scholar] [CrossRef] [PubMed]
- Ochyra, R.; Smith, R.I.L.; Bednarek-Ochyra, H. The Illustrated Moss Flora of Antarctica, 1st ed.; Cambridge University Press: Cambridge, UK, 2008; ISBN 978-0-521-81402-7. [Google Scholar]
- Segovia, R.; Armesto, J.J. The Gondwanan legacy in South American biogeography. J. Biogeogr. 2015, 42, 209–217. [Google Scholar] [CrossRef]
- Barreda, V.D.; Palazzesi, L.; Pujana, R.R.; Panti, C.; Tapia, M.J.; Fernández, D.A.; Noetinger, S. The Gondwanan heritage of the Eocene–Miocene Patagonian floras. J. S. Am. Earth Sci. 2021, 107, 103022. [Google Scholar] [CrossRef]
- Vanderpoorten, A.; Gradstein, S.R.; Carine, M.A.; Devos, N. The ghosts of Gondwana and Laurasia in modern liverwort distributions. Biol. Rev. 2010, 85, 471–487. [Google Scholar] [CrossRef] [PubMed]
- Convey, P.; Biersma, E.M.; Casanova-Katny, A.; Maturana, C.S. Refuges of Antarctic diversity. In Past Antarctica: Paleoclimatology and Climate Change, 1st ed.; Oliva, M., Ruiz-Fernández, J., Eds.; Academic Press: New York, NY, USA, 2020; pp. 181–200. ISBN 978-0-12-817925-3. [Google Scholar]
- Stevens, M.I.; Mackintosh, A.N. Location, location, location: Survival of Antarctic biota requires the best real estate. Biol. Lett. 2023, 19, 20220590. [Google Scholar] [CrossRef] [PubMed]
- Hughes, K.A.; Ireland, L.; Convey, P.; Fleming, A.H. Assessing the effectiveness of specially protected areas for conservation of Antarctica’s botanical diversity. Conserv. Biol. 2016, 30, 113–120. [Google Scholar] [CrossRef] [PubMed]
- Huiskes, A.H.L.; Gremmen, N.J.M.; Bergstrom, D.M.; Frenot, Y.; Hughes, K.A.; Imura, S.; Kiefer, K.; Lebouvier, M.; Lee, J.E.; Tsujimoto, M.; et al. Aliens in Antarctica: Assessing transfer of plant propagules by human visitors to reduce invasion risk. Biol. Conserv. 2014, 171, 278–284. [Google Scholar] [CrossRef]
- Coronato, A.; Borromei, A.M.; Ponce, J.F.; Candel, S.; Musotto, L.; Fernández, M.; Laprida, C.; Mehl, A.; Montes, A.; San-Martín, C.; et al. Holocene environmental changes in the fuegian forest and steppe, Argentina. J. S. Am. Earth Sci. 2022, 119, 103952. [Google Scholar] [CrossRef]
- Unkel, I.; Fernandez, M.; Björcka, S.; Ljung, K.; Wohlfarth, B. Records of environmental changes during the Holocene from Isla de los Estados (54.4°S), southeastern Tierra del Fuego. Glob. Planet. Change 2010, 74, 99–113. [Google Scholar] [CrossRef]
- Reynhout, S.; Sagredo, E.; Kaplan, M.; Aravena, J.C.; Martini, M.; Moreno, P.; Rojas, M.; Schwartz, R.; Schaefer, J. Holocene glacier fluctuations in Patagonia are modulated by summer insolation intensity and paced by Southern Annular Mode-like variability. Quat. Sci. Rev. 2019, 220, 178–187. [Google Scholar] [CrossRef]
- Galloway, D.J. Flora of New Zealand: Lichens, Including Lichen-Forming and Lichenicolous Fungi. Revised Second Edition, 2nd ed.; Manaaki Whenua Press: Lincoln, New Zealand, 2007; ISBN 987-0-478-09376-6. [Google Scholar]
- Sancho, L.; De Los Ríos, A.; Pintado, A.; Colesie, C.; Raggio, J.; Ascaso, C.; Green, A. Himantormia lugubris, an Antarctic endemic on the edge of the lichen symbiosis. Symbiosis 2020, 82, 49–58. [Google Scholar] [CrossRef]
- Colesie, C.; Walshaw, C.V.; Sancho, L.G.; Davey, M.P.; Gray, A. Antarctica’s vegetation in a changing climate. Wiley Interdiscip. Rev. Clim. Change 2023, 14, e810. [Google Scholar] [CrossRef]
Figure 1.
Frequency plot of the shared species between Navarino Island and the South Shetland Islands according to their distribution, habitat, and substrate type on Navarino Island. Relative species abundance is expressed with respect to habitat.
Figure 1.
Frequency plot of the shared species between Navarino Island and the South Shetland Islands according to their distribution, habitat, and substrate type on Navarino Island. Relative species abundance is expressed with respect to habitat.
Figure 2.
Frequency plot of the shared species between Navarino Island and the South Shetland Islands according to their distribution and substrate type on Navarino Island.
Figure 2.
Frequency plot of the shared species between Navarino Island and the South Shetland Islands according to their distribution and substrate type on Navarino Island.
Table 1.
Shared species between Navarino Island and the South Shetland Islands. Endemic stands for Antarctic–subantarctic endemic.
Table 1.
Shared species between Navarino Island and the South Shetland Islands. Endemic stands for Antarctic–subantarctic endemic.
| Distribution | Species | Habitat | Substrate Type | ||||
|---|---|---|---|---|---|---|---|
| Coastal | Forest | Alpine | Epiphytic | Saxicolous | Terricolous | ||
| bipolar | Acarospora badiofusca (Nyl.) Th. Fr. | + | + | ||||
| cosmopolitan | Agonimia tristicula (Nyl.) Zahlbr. | + | + | ||||
| bipolar | Amandinea punctata (Hoffm.) Coppins & Scheid. | + | + | + | |||
| bipolar | Arthrorhaphis citrinella (Ach.) Poelt | + | + | ||||
| endemic | Austroplaca ambitiosa (Darb.) Søchting, Frödén & Arup | + | + | ||||
| endemic | Austroplaca cirrochrooides (Nyl.) Søchting, Frödén & Arup s.lat. | + | + | ||||
| endemic | Austroplaca millegrana (Müll. Arg.) Søchting, Frödén & Arup s.lat. | + | + | ||||
| cosmopolitan | Baeomyces rufus (Huds.) Rebent. | + | + | ||||
| austral | Bibbya bullata (Meyen & Flot.) Kistenich, Timdal, Bendiksby & S. Ekman | + | + | + | + | ||
| bipolar | Caloplaca phaeocarpella (Nyl.) Zahlbr | + | + | ||||
| cosmopolitan | Candelariella vitellina (Ehrh.) Müll. Arg. | + | + | ||||
| bipolar | Carbonea vorticosa (Flörke) Hertel | + | + | + | |||
| bipolar | Catapyrenium cinereum (Pers.) Körb. | + | + | ||||
| bipolar | Cetraria aculeata (Schreb.) Fr. | + | + | ||||
| bipolar | Cetraria islandica (L.) Ach. | + | + | ||||
| bipolar | Chrysothrix chlorina (Ach.) J. R. Laundon | + | + | ||||
| austral | Cladia aggregata (Sw.) Nyl. | + | + | + | |||
| bipolar | Cladonia asahinae J.W. Thompson | + | + | + | |||
| bipolar | Cladonia bellidiflora (Ach.) Schaerer | + | + | + | |||
| bipolar | Cladonia borealis Stenroos | + | + | + | |||
| bipolar | Cladonia carneola (Fr.) Fr. | + | + | ||||
| endemic | Cladonia cervicornis spp. mawsonii (C.W. Dodge) S. Stenroos & Ahti | + | + | ||||
| cosmopolitan | Cladonia chlorophaea (Flörke ex Sommerf.) Spreng. | + | + | + | + | ||
| cosmopolitan | Cladonia cornuta (L.) Hoffm. | + | + | + | |||
| cosmopolitan | Cladonia fimbriata (L.) Fr. | + | + | ||||
| bipolar | Cladonia gracilis (L.) Willd. | + | + | + | |||
| endemic | Cladonia lepidophora Ahti & Kashiw. | + | + | ||||
| bipolar | Cladonia mitis Sandst. | + | + | + | |||
| endemic | Cladonia novochlorophaea (Sipman) Brodo & Ahti | + | + | ||||
| bipolar | Cladonia phyllophora Hoffm. | + | + | ||||
| bipolar | Cladonia pleurota (Flörke) Schaerer | + | + | ||||
| cosmopolitan | Cladonia pocillum (Ach.) Grognot | + | + | ||||
| cosmopolitan | Cladonia pyxidata (L.) Hoffm. | + | + | ||||
| bipolar | Cladonia rangiferina (L.) Weber ex Wigg. | + | + | + | |||
| austral | Cladonia sarmentosa (Hook f. & Taylor) C.W. Dodge | + | + | ||||
| bipolar | Cladonia scabriuscula (Delise) Nyl. | + | + | ||||
| cosmopolitan | Cladonia squamosa (Scop.) Hoffm. | + | + | ||||
| austral | Cladonia subsubulata Nyl. | + | + | ||||
| bipolar | Cladonia subulata (L.) F.H. Wigg. | + | + | ||||
| bipolar | Cladonia sulphurina (Michaux) Fr. | + | + | + | |||
| austral | Cladonia ustulata (Hook. F. & Taylor) Leight. | + | + | + | |||
| austral | Coccotrema cucurbitula (Mont.) Müll. Arg. | + | + | + | + | ||
| austral | Coelopogon epiphorellum (Nyl.) Brusse & Kärnefelt | + | + | + | + | ||
| bipolar | Cystocoleus ebeneus (Dillwyn) Twaites | + | + | + | + | ||
| bipolar | Frutidella caesioatra (Schaer.) Kalb | + | + | ||||
| austral | Gondwania sublobulata (Nyl.) S.Y. Kondr., Kärnefelt, Elix, A. Thell, J. Kim, M.-H. Jeong, N.-N. Yu, A.S. Kondr. & Hur | + | + | ||||
| bipolar | Gowardia nigricans (Ach.) Halonen | + | + | + | |||
| endemic | Haematomma erythromma (Nyl.) Zahlbr. | + | + | + | |||
| cosmopolitan | Hydropunctaria maura (Wahlenb.) C. Keller, Gueidan & Thüs | + | + | ||||
| bipolar | Hypogymnia lugubris var. lugubris (Pers.) Krog | + | + | + | |||
| bipolar | Japewia tornoensis (Nyl.) Tønsberg | + | + | + | |||
| bipolar | Lecanora epibryon (Ach.) Ach. | + | + | ||||
| cosmopolitan | Lecanora flotoviana Spreng. | + | + | ||||
| bipolar | Lecanora intricata (Ach.) Ach. | + | + | ||||
| endemic | Lecanora physciella (Darb.) Hertel | + | + | + | + | ||
| bipolar | Lecanora polytropa (Hoffm.) Rabenh. | + | + | ||||
| bipolar | Lecidea atrobrunnea (Ram. ex Lam. et DC.) Schaerer | + | + | ||||
| bipolar | Lecidella elaeochroma (Ach.) M. Choisy | + | + | ||||
| bipolar | Lecidella patavina (A. Massal.) Knoph & Leuckert | + | + | ||||
| bipolar | Lecidella stigmatea (Ach.) Hertel & Leuckert | + | + | ||||
| bipolar | Lecidella wulfenii (Hepp) Körb. | + | + | ||||
| bipolar | Lecidoma demissum (Rustr.) Gotth. Schneid. & Hertel | + | + | ||||
| bipolar | Lepraria caesioalba (B. de Lesd.) J.R. Laundon | + | + | + | + | + | |
| endemic | Leptogium menziesii (Ach.) Mont. | + | + | + | |||
| endemic | Leptogium puberulum Hue | + | + | ||||
| bipolar | Massalongia patagonica Kitaura & Lorenz | + | + | + | |||
| bipolar | Mastodia tessellata (Hook. f. & Harv.) Hook. f. & Harv. | + | + | ||||
| bipolar | Megalaria grossa (Pers. ex Nyl.) Hafellner | + | + | + | |||
| bipolar | Megaspora verrucosa (Ach.) Hafellner & V. Wirth | + | + | + | |||
| cosmopolitan | Melanohalea elegantula (Zahlbr.) O. Blanco, A. Crespo, Divakar, Essl., D. Hawksw. & Lumbsch | + | + | ||||
| endemic | Melanohalea ushuaiensis (Zahlbr.) O. Blanco et al. | + | + | + | + | ||
| endemic | Menegazzia magellanica R. Sant. | + | + | + | |||
| bipolar | Micarea incrassata Hedl. | + | + | ||||
| bipolar | Mycobilimbia hypnorum (Lib.) Kalb & Hafellner | + | + | ||||
| austral | Notoparmelia cunninghamii (Cromb.) A. Crespo, Ferencová & Divakar | + | + | ||||
| endemic | Ochrolechia antarctica (Müll. Arg.) Darb. | + | + | + | |||
| bipolar | Ochrolechia frigida (Sw.) Lynge | + | + | + | |||
| bipolar | Pannaria hookeri (Borrer ex Sm.) Nyl. | + | + | + | |||
| cosmopolitan | Parmelia saxatilis (L.) Ach. | + | + | + | |||
| cosmopolitan | Peltigera didactyla (With.) J.R. Laundon | + | + | ||||
| cosmopolitan | Peltigera rufescens (Weiss) Humb. | + | + | ||||
| endemic | Peltularia fuegiana Henssen & P.M. Jørg. | + | + | + | + | + | |
| endemic | Pertusaria spegazzinii Müll. Arg. | + | + | ||||
| bipolar | Phaeophyscia endococcina (Körb.) Moberg | + | + | ||||
| cosmopolitan | Physcia caesia (Hoffm.) Fürnr. | + | + | ||||
| cosmopolitan | Physcia dubia (Hoffm.) Lettau | + | + | ||||
| bipolar | Physconia muscigena (Ach.) Poelt | + | + | ||||
| cosmopolitan | Placidium squamulosum (Ach.) O. Breuss | + | + | ||||
| endemic | Poeltidea perusta (Nyl.) Hertel & Hafellner | + | + | + | + | ||
| bipolar | Polycauliona candelaria (L.) Frödén, Arup & Søchting | + | + | + | + | + | |
| bipolar | Pseudephebe minuscula (Nyl.) Brodo & D. Hawksw. | + | + | ||||
| endemic | Psoroma antarcticum Hong & Elvebakk | + | + | ||||
| endemic | Psoroma cinnamomeum Malme | + | + | + | + | ||
| austral | Psoroma fruticulosum James & Henssen | + | + | ||||
| cosmopolitan | Psoroma hypnorum (Vahl) Gray | + | + | ||||
| endemic | Ramalina terebrata Hook. & Taylor | + | + | ||||
| bipolar | Rhizocarpon geminatum Körb. | + | + | + | |||
| bipolar | Rhizocarpon geographicum (L.) DC. | + | + | + | + | ||
| bipolar | Rhizocarpon polycarpum (Hepp) Th. Fr. | + | + | ||||
| bipolar | Rinodina olivaceobrunnea C.W. Dodge & G.E. Baker | + | + | + | |||
| austral | Rinodina peloleuca (Nyl.) Müll. Arg. | + | + | ||||
| cosmopolitan | Sarcogyne privigna (Ach.) A. Massal. | + | + | ||||
| austral | Siphulastrum mamillatum (Hook. F. & Taylor) D.J. Galloway | + | + | ||||
| cosmopolitan | Sphaerophorus globosus (Huds.) Vainio | + | + | ||||
| bipolar | Sporastastia testudinea (Ach.) A. Massal. | + | + | ||||
| bipolar | Stereocaulon alpinum Laurer | + | + | + | |||
| austral | Stereocaulon glabrum (Müll. Arg.) Vain. | + | + | ||||
| cosmopolitan | Tephromela atra (Huds.) Hafellner | + | + | ||||
| bipolar | Toniniopsis bagliettoana (A. Massal. & De Not.) Kistenich & Timdal | + | + | ||||
| bipolar | Trapeliopsis granulosa (Hoffm.) Lumbsch | + | + | ||||
| bipolar | Tremolecia atrata (Ach.) Hertel | + | + | ||||
| bipolar | Umbilicaria decussata (Vill.) Zahlbr. | + | + | ||||
| bipolar | Umbilicaria nylanderiana (Zahlbr.) H. Magn. | + | + | ||||
| bipolar | Umbilicaria umbilicarioides (Stein.) Krog & Swinscow | + | + | ||||
| austral | Usnea aurantiaco-atra (Jacq.) Bory | + | + | ||||
| bipolar | Usnea cf. sphacelata R. Br. | + | + | + | + | + | |
| endemic | Usnea subantarctica F.J. Walker | + | + | ||||
| austral | Usnea trachycarpa (Stirton) Müll. Arg. | + | + | ||||
| endemic | Verrucaria dispartita Vain. | + | + | ||||
| austral | Verrucaria durietzii I.M. Lamb | + | + | ||||
| bipolar | Verrucaria halizoa Leight. | + | + | ||||
| bipolar | Verrucaria margacea (Wahlenb. in Ach.) Wahlenb. | + | + | ||||
| austral | Verrucaria tesselatula Nyl. | + | + | ||||
| cosmopolitan | Xanthoria elegans (Link) Th. Fr. | + | + | ||||
The symbol + indicates which habitat and substrate type categories apply to each species.
Table 2.
Abundance of the main morphotypes of the shared species between Navarino Island and the South Shetland Islands.
Table 2.
Abundance of the main morphotypes of the shared species between Navarino Island and the South Shetland Islands.
| Morphology | Absolute Abundance | Relative Abundance |
|---|---|---|
| crustose | 56 | 45.2% |
| foliose | 28 | 22.6% |
| fruticose | 16 | 12.9% |
| cladonoid | 24 | 19.3% |
Table 3.
Three-way contingency table of the shared species between Navarino Island and the South Shetland Islands according to their distribution, habitat, and substrate type on Navarino Island. Relative species abundance is expressed with respect to habitat.
Table 3.
Three-way contingency table of the shared species between Navarino Island and the South Shetland Islands according to their distribution, habitat, and substrate type on Navarino Island. Relative species abundance is expressed with respect to habitat.
| Habitat | Substrate Type | Distribution | |||
|---|---|---|---|---|---|
| Endemic | Austral | Bipolar | Cosmopolitan | ||
| coastal | epiphytic | 1.7% | 3.3% | 10.0% | 0.0% |
| saxicolous | 16.7% | 10.0% | 25.0% | 13.3% | |
| terricolous | 0.0% | 5.0% | 10.0% | 5.0% | |
| forest | epiphytic | 7.0% | 7.0% | 9.3% | 2.3% |
| saxicolous | 4.7% | 2.3% | 14.0% | 0.0% | |
| terricolous | 7.0% | 4.7% | 23.3% | 18.6% | |
| alpine | epiphytic | 2.4% | 1.2% | 9.5% | 0.0% |
| saxicolous | 9.5% | 4.8% | 23.8% | 3.6% | |
| terricolous | 7.1% | 4.8% | 28.6% | 4.8% | |
Table 4.
Two-way contingency table of the shared species between Navarino Island and the South Shetland Islands according to their habitat and substrate type on Navarino Island.
Table 4.
Two-way contingency table of the shared species between Navarino Island and the South Shetland Islands according to their habitat and substrate type on Navarino Island.
| Substrate Type | Habitat | ||
|---|---|---|---|
| Coastal | Forest | Alpine | |
| epiphytic | 15.0% | 25.6% | 13.1% |
| saxicolous | 65.0% | 20.9% | 41.7% |
| terricolous | 20.0% | 53.5% | 45.2% |
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MDPI and ACS Style
Sancho, L.G.; Aramburu, A.; Etayo, J.; Beltrán-Sanz, N. Floristic Similarities between the Lichen Flora of Both Sides of the Drake Passage: A Biogeographical Approach. J. Fungi 2024, 10, 9. https://doi.org/10.3390/jof10010009
AMA Style
Sancho LG, Aramburu A, Etayo J, Beltrán-Sanz N. Floristic Similarities between the Lichen Flora of Both Sides of the Drake Passage: A Biogeographical Approach. Journal of Fungi. 2024; 10(1):9. https://doi.org/10.3390/jof10010009
Chicago/Turabian StyleSancho, Leopoldo G., Ana Aramburu, Javier Etayo, and Núria Beltrán-Sanz. 2024. "Floristic Similarities between the Lichen Flora of Both Sides of the Drake Passage: A Biogeographical Approach" Journal of Fungi 10, no. 1: 9. https://doi.org/10.3390/jof10010009
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