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Delmarva Lichens: An illustrated manual

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***AVAILABLE ONLINE VIA JSTOR: https://www.jstor.org/stable/e26976761 Delmarva (also known as the Delmarva Peninsula), the name itself at once invites questions and invokes history. Just as the name is an aggregation (of Delaware, Maryland and Virginia), so is the land an aggregation of floras and faunas, of political units and cultures, of times and places. Situated between the Chesapeake Bay, America’s beleaguered estuarine jewel, the Delaware Bay, an area of critical global importance to migrating shorebirds, and the inexorably rising waters of the Atlantic Ocean, Delmarva is a vast peninsula defined by coexistence and contrasts, a meeting place of north and south, of urban and rural, of past and future. Like Delmarva, lichens are also defined by coexistence and contrast. They are among the most remarkable products of evolution: fungi that have entered into obligate symbioses with algae and cyanobacteria. Together the two form complex and striking structures unlike any other in nature. While this specialized lifestyle has allowed lichens to survive, and even thrive, in nearly every ecosystem on land, it also means these fungi cannot survive on their own. In fact, lichens are extremely sensitive to habitat loss, degradation and disturbance. Lichens have long been an integral component of the Delmarva landscape. They serve important functions in the environment, supplying food and shelter for animals, and providing ecosystem services that ultimately benefit human welfare and society. As we show in this book, while the link between lichens and Delmarva in the past is clear, how exactly they fit into the narrative for the future of Delmarva is an open question. We wrote this book with the goal of providing a resource that would open the world of these neglected species to anyone who wanted to learn about them. Our work draws on more than four years of detailed study in the region, trudging through swamps and reveling in beaches. There are many resources to learn about, identify and appreciate other groups of Delmarva biodiversity, such as birds and wildflowers. Yet to date there has never been such a resource for lichens. In this volume we treat the 299 species of lichens that have been documented from Delmarva to date, all of which are presumed to be native. This includes not just the macrolichens, some of which have been treated elsewhere, but also the microlichens that have long been neglected in North American floras. For each species, we provide a description, a discussion of its distribution and ecology, a proposed conservation rank, and a comparison with similar species. We have also assembled a discussion of Delmarva natural history, checklists that are arranged alphabetically and evolutionarily, and a complete set of identification keys. A distribution map for each species is also included that shows the range of the species in the context of the broader Washington D.C. metro region, and contrasts the historical occurrences with those from modern times. Nearly all of the species are illustrated with color photographs. Our hope is that publication of this work will prove to be a turning point for the lichens in the Mid-Atlantic Region, serving as inspiration to explore and appreciate a long-neglected component of biodiversity. While the book focuses on Delmarva, it covers the majority of species that occur along the Atlantic Coast from Norfolk, Virginia, to Cape Cod, Massachusetts. Thus the area covered by this book includes the metropolitan areas of Washington, D.C., Philadelphia and New York.
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... Punctelia missouriensis can be distinguished from the other six species of Punctelia found in the Great Lakes Basin by its pale brown lower surface and laminal, partially corticate, squamiform isidia often arising from pseudocyphellae, with typically fewer than ten per pseudocyphella and medulla containing lecanoric acid (Aptroot 2003, Lendemer & Noell 2018. The most frequently encountered Punctelia in the study area is P. rudecta (Ach.) ...
... Brinker unpublished data) which is also isidiate. It can readily be distinguished from P. missouriensis by its taller, branched, corticate isidia with brown tips that do not resemble coarse masses of soredia mounded in a soralium (Lendemer & Noell 2018). Punctelia bolliana (Müll. ...
... The cushion-forming tendency of the species with its prostrate, yellow-green (usnic acid) irregularly-branched, corticate podetia make it recognizable in the field along with its chemistry (KC+ yellow, UV-) (Lendemer & Noell 2018). The inner podetial walls (stereome) are composed of long cartilaginous strands or cords (Hinds & Hinds 2007). ...
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Noteworthy records of forty-three lichens and allied fungi are presented based on recent collections from Ontario, Canada. Three species, Agonimia borysthenica, Arthonia subconveniens (on Ricasolia quercizans) and Lecanographa abscondita are reported for the first time from North America. Eleven species, Erythricium aurantiacum (on Physcia millegrana), Hypotrachyna showmanii, Leptogium arsenei, Opegrapha rupestris (on Bagliettoa), Pronectria tibellii (on Cladonia pocillum), Punctelia missouriensis, Thelidium zwackhii, Tremella imshaugiae (on Imshaugia aleurites), Verrucaria bryoctona, Vezdaea schuyleriana and Vouauxiella lichenicola (on Lecanora) are reported for the first time from Canada. Eleven species, Absconditella sphagnorum, Agonimia gelatinosa, Didymocyrtis xanthomendozae (on Xanthomendoza hasseana), Distopyrenis americana, Lichenochora obscuroides (on Phaeophyscia pusilloides and P. sciastra), Paranectria oropensis (on Lecanora and P. rubropulchra), Pertusaria sommerfeltii, Raesaenenia huuskonenii (on Bryoria fuscescens), Stereocaulon depreaultii, Thrombium epigaeum and Trichonectria rubefaciens (on Aspicilia) are reported as new to Ontario. Details on 18 additional rare or otherwise rarely collected species new to various counties and districts of the province are also provided. These include: Abrothallus microspermus (on Flavoparmelia caperata), Ahtiana aurescens, Athelia arachnoidea (on Physcia millegrana), Blennothallia crispa, Chaenothecopsis brevipes (on Inoderma byssaceum), C. rubescens (on I. byssaceum), Cladonia dimorphoclada, Corticifraga fuckelii (on Peltigera evansiana), Didymocyrtis cladoniicola (on Cladonia), Hypotrachyna revoluta, Lepra panyrga, Marchandiomyces corallinus (on Parmelia squarrosa and Physcia thomsoniana), Muellerella hospitans (on Bacidia rubella), Refractohilum peltigerae (on Peltigera evansiana), Reichlingia leopoldii, Sarcosagium campestre, Steinia geophana and Vezdaea acicularis.
... Herpothallon rubrogranulosum appears to be infrequent but widespread in the southern portions of the Mid-Atlantic Coastal Plain of eastern North America where it occurs from southern North Carolina south to Georgia near the border with Florida, USA (Fig. 1). Extensive lichen inventory work has been carried out in adjacent areas of the Coastal Plain, further north in the Mid-Atlantic Coastal Plain (Allen and Lendemer 2016, Lendemer and Noell 2018, east throughout the State of Georgia (M.F. Hodges and S.Q. ...
... might be confused with the new species due to the presence of psoromic acid and similar ecorticate, crustose thallus (Muscavitch et al. 2017). However, that species has a coccoid rather than trentepohlioid photobiont and is blue-gray or white in color because it does not produce red pigments (Lendemer and Harris 2014, Muscavitch et al. 2017, Lendemer and Noell 2018. Damaged or discolored thalli of Lepra pustulata (Brodo & W.L. Culb.) ...
... Lendemer & R.C.Harris could potentially also be confused with the new species because they are pustulose and can develop a pinkish hue that is especially noticeable in older herbarium specimens (Brodo and Culberson 1986). Nonetheless, L. pustulata is easily distinguished by the presence of a shiny cortex, coccoid photobiont, and the production of thamnolic acid, which is readily separated from psoromic acid by spot tests (Kþ intense yellow, Pþ orange in thamnolic acid vs. KÀ and Pþ intense yellow in psoromic acid; Lendemer and Noell 2018). Occasional forms of Loxospora confusa Lendemer and Megalaria alleniae Lendemer & McMullin might also be confused with H. rubrogranulosum on account of the thalli that can appear to be granular from a distance. ...
Article
Herpothallon rubrogranulosum is described from forested wetlands in the Mid-Atlantic Coastal Plain of southeastern North America. It appears to be infrequent throughout its range, but locally abundant on bald cypress trees in areas of Francis Marion National Forest, South Carolina, USA. The species is characterized by a cream colored, ecorticate thallus with small, coarse granular pseudoisidia that are covered with variable amounts of orange-red pigment that reacts K+ red-pink, and the production of abundant psoromic acid. It was previously confused with H. rubroechinatum, which is a rarer tropical species that differs markedly in having large, conspicuous pseudoisidia.
... Arg.) R.W. Rogers. Asci and ascospores are required to discern between these two species (Lendemer & Noell 2018), and given that both occur in the southern Appalachian Mountains either is possible (Lendemer & Westberg 2010 This species is known from scattered locations throughout the the Coastal Plain of southeastern North America (e.g., Harris 1995), but there are few reports from very far inland. Externally it is very similar to C. caroliniana, which is much more common and differs in the production of perlatolic acid rather than protocetraric acid in the medulla (Hale 1976, Lendemer & Ruiz 2015. ...
... As has been discussed elsewhere, this is a common phenomenon in North America and such material should not necessarily be discarded because it is important records in most regions where it is presumed that only the common and widely distributed C. pyrrhula (Nyl.) Grube occurs (e.g., Lendemer & Noell 2018. Although our material cannot be determined with certainty, it likely represents C. pyrrhula. ...
... Quercus, Lendemer 53084. Schismatomma glaucescens is a somewhat enigmatic species that has only recently been treated in detail with published illustrations (Lendemer & Noell 2018, Tripp & Lendemer 2020. It was recognized by Harris (1990), who reported it from scattered locations in eastern North America. ...
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In the spring of 2017, the 26th Tuckerman Workshop was held in central Alabama, based in Columbiana. Participants collected lichens from six unique sites across the hills of central Alabama. An account of the lichens collected from five of those sites are presented here. A total of 274 species from 118 genera are reported from the region based on field collections of the workshop participants. The high levels of diversity documented are equal to or greater than the diversity found in other areas inventoried in southern Appalachian Mountain habitats in northern and central Alabama. There are 31 lichenized and lichenicolous taxa newly reported for the State of Alabama: Abrothallus hypotrachynae (host: Hypotrachyna), Arthonia stevensoniana (host: Haematomma), Aspicilia laevata, Asterothyrium decipiens, Bacidina delicata, Byssoloma maderense, Canoparmelia amazonica, Carbonea latypizodes, Carbonicola anthracophila, Catillaria nigroclavata, Chrysothrix insulizans, Dictyomeridium amylosporum, Fellhanera silicis, Fuscidea arcuatula, Graphis lineola, Haematomma guyanense, Homostegia hertelii (host: Flavoparmelia baltimorensis), Ionaspis alba, Loxospora confusa, Parmotrema neotropicum, Pseudosagedia guentheri, Psilolechia lucida, Ramonia microspora, Rinodina dolichospora, Schismatomma glaucescens, Skyttea lecanorae (host: Lecanora louisianae), Thelopsis rubella, Thelotrema lathraeum, Tricharia cuneata, Usnea cornuta and Vainionora americana. In addition, an incompletely determined specimen of Coniarthonia was collected, making this a new genus report for the state.
... Five lichenologists who work regularly in our target regions were consulted for this project. The characteristics of the recommended species, the most likely lookalike species for each, and the likelihood that nonspecialists could be trained to reliably distinguish recommended species from others were also evaluated, using details given in taxonomic treatments for the regions (Harris 1990;Brodo et al. 2001;DeBolt et al. 2007;Lendemer et al. 2013;Brodo 2016;Lendemer & Noell 2018;Harris & Ladd 2019). James Lendemer (ibid.) is a professional lichenologist at the New York Botanical Garden with extensive experience, collections, and publications on lichens in the Mid-Atlantic and Southeast FIA regions. ...
... Beeching and Hodges reported that Physcia aipolia is not found in Georgia; their collections identified by James Lendemer are the physically and chemically similar P. pumilior described by Harris (1990) from Florida. Lendemer reported that P. pumilior rather than P. aipolia is found through most of the central and eastern parts of the Mid-Atlantic FIA region (Lendemer & Noell 2018). Brodo et al. (2013), citing specimens from four northern North American herbaria and all New York Botanical Garden collections (NYBG 2019), reflected that P. aipolia does not occur in the eastern half of the Mid-Atlantic region (sensu Fig. 1) nor in Southeast region states, where P. pumilior is widespread and common. ...
... An earlier recommendation to evaluate composite Physcia aipolia/pumilior/stellaris for better coverage of urban and other locations with less nearby forested landcover is supported for Virginia, where this group has no environmental limitations (absent from Tables 2, 3). The clear differences in species frequency and response to environment between Virginia and the other four Southeast region states (Tables 1-3) are consistent with a strong north-south gradient in lichen species composition for this region noted by McCune et al. (1997) and documented in greater detail by Lendemer and Noell (2018) and Lendemer et al. (2016). The frequencies (Table 1) confirm Virginia as intermediate and Table 3. Regression models that explain >10% of variation in lichen species abundance. ...
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Lichen element (N, S, metals) indicators of local air pollution load (a widely used technique) are recommended for five predefined regions covering central and southern parts of the eastern United States. The final recommendations integrate the advice of regional lichenologists, information from regional floras, and species abundance data from a United States Forest Service Forest Inventory and Analysis Program (FIA) lichen database for 11 of the 21 covered eastern states. Recommended species were frequent in their region, easy for nonspecialists to distinguish in the field after training, and easy to handle using clean protocols. Regression models of species abundance in FIA plots from five southeastern states vs. climate, air pollution (both from a regional lichen response model) and type of nearby landcover (from the National Land Cover Database) identified species’ environmental limitations. Punctelia rudecta is recommended for cooler forested uplands of all regions, with three Physcia species combined and Punctelia missouriensis for isolated woodlands or urban areas of three regions. Parmotrema hypotropum and P. hypoleucinum combined (weak environmental limitation) or P. perforatum . and P. subrigidum combined (limited in more polluted areas) are recommended for warmer Coastal Plains in two regions each. Additional species are recommended for single regions. Each species must be quantitatively evaluated in each region, to demonstrate indication reliability in practice and to calculate element data conversions between species for region-wide bioindication.
... With the exception of L. finkii, these species were found in all four physiographic regions. The frequency of these species throughout the study area is logical as they are common and widely distributed in the Mid-Atlantic Region of eastern North America (e.g., Brodo et al. 2001, Hinds & Hinds 2007, Lendemer & Noell 2018. The absence of saxicolous lichens from the most frequent taxa likely reflects the scarcity of rock substrates in the Coastal Plain. ...
... All four species were rare in the study area, and only L. cyanescens was found at more than one location. The overall rarity of cyanolichens in Mercer County is similar to other areas with fragmented natural landscapes in temperate eastern North America (e.g., Lendemer & Noell 2018), where L. cyanescens in particular is often the only species encountered with any degree of frequency. It is important to highlight that, based on historical records of lichens from elsewhere in New Jersey (Waters & Lendemer in press.), the rarity of cyanolichens in modern times is almost certainly not reflective of the past distribution or abundance of these taxa. ...
... The non-saxicolous taxa unique to the Piedmont include common and widely distributed species such as Cladonia cylindrica (3 sites), C. peziziformis (4), C. rei (3), Micarea prasina (3), Phaeocalicium polyporaeum (4), Physciella chloantha (3), and Placynthiella icmalea (3) , Hinds & Hinds 2007, Lendemer & Noell 2018. The absence of Physciella chloantha from the Coastal Plain is particularly noteworthy give that it occurs on roadside trees in coastal areas of the Mid-Atlantic (Allen & Howe 2016, Lendemer & Noell 2018. ...
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A checklist of the lichens and allied fungi from Mercer County, New Jersey, is presented. It was derived from inventories of 14 tracts of preserved and undeveloped land, which yielded 905 collections and 174 taxa. These include 37 new records for New Jersey, two of which, Catinaria neuschildii and Strangospora pinicola, have been rarely reported from North America. It also includes Agonimia flabelliformis, which is newly reported for North America from localities throughout the Appalachian and Ozark Mountains. Catillaria patteeana is described as new to science as well. These inventories demonstrate that substantial lichen diversity remains undiscovered even in densely populated regions of the Mid-Atlantic characterized by highly fragmented and disturbed natural landscapes with relatively small areas of unaltered, contiguous core-natural habitat.
... Lecanora protervula is common and widespread in forested habitats at middle to low elevations where it occurs primarily on the bark and branches of hardwood trees and shrubs (see Imshaug and Brodo 1966, Lendemer and Noell 2018, Tripp and Lendemer 2020. ...
... The primarily threats to Lecanora protervula are urbanization and commercial development as it does not typically occur in densely urban areas. Otherwise it appears to be tolerant of disturbance (Lendemer and Noell 2018). ...
... Elsewhere in its North American range it is can be common to locally abundant on trees (rarely rocks) in a wide variety of upland and lowland situations, usually in relatively welllit environs (e.g. Lendemer & Noell 2018). (Brodo et al. 2001), but can also occur in anthropogenic-influenced habitat such as urban parks and suburbs of cities more so in the centre of its range (e.g. ...
... Gray, particularly S. tenuissimum They can be distinguished from P. muscicola by their thalli that are usually initially composed of wrinkled lobes that are either fimbriately torn along their margins or are isidioid, and their muriform ascospores (Jørgensen 2012a). A specimen reported by Lewis and Brinker (2017) -Porina scabrida is a widespread and common crustose lichen found throughout southeastern North America and the Ozarks, though can be easily overlooked because it is usually sterile, and its appearance in the field is akin to alga (Harris 1995, Lendemer & Noell 2018. It is an epiphytic lichen with a richly isidiate, paleolive to orangish thallus, with cylindrical isidia consisting mostly of the photobiont with an external unicellular fungal layer (Harris 1995). ...
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One-hundred and sixty-three new or noteworthy lichens and allied fungi are reported from Ontario based on new collections. The lichens Lecanora atromarginata, L. gisleriana, Rhizocarpon ridescens and Sclerococcum griseisporodochium are new to North America. The reported species new to Canada are: Abrothallus bertianus, Absconditella trivialis, Agonimia opuntiella, Diploschistes gypsaceus, Ephebe solida, Heterodermia japonica, Minutoexcipula tuckerae, Peltula bolanderi, Placynthium petersii, Protothelenella sphinctrinoides, Pycnora praestabilis, Thelopsis melathelia, Toninia tecta and Verrucaria quercina. Sixty-one taxa reported new to Ontario include: Abrothallus peyritschii, A. usneae, Agonimia tristicula, Arctoparmelia subcentrifuga, Arthrorhaphis citronella, Bachmanniomyces uncialicola, Baeomyces placophyllus, Biatora printzenii, Bilimbia lobulata, Calicium lucidum, Caloplaca stillicidiorum, Cetraria nigricans, Chaenothecopsis australis, Cystocoleus ebeneus, Dactylospora lobariella, Dendriscocaulon intricatulum, Dermatocarpon schaechtelinii, Enchylium conglomeratum, Endocarpon pulvinatum, Gyrographa gyrocarpa, Henrica theleodes, Heterodermia neglecta, Homostegia piggotii, Hypotrachyna afrorevoluta, H. revoluta, Lathagrium auriforme, Lecanora appalachensis, Lecanora epibryon, Lecanora orae-frigidae, Lecidea lapicida, Lecidella wulfenii, Lempholemma radiatum, Lepraria oxybapha, Lichenoconium usneae, Lichenomphalia umbellifera, Lichenostigma elongata, Lopadium coralloideum, Ophioparma lapponica, Pertusaria bryontha, P. coriacea, P. globularis, Phylliscum demangeonii, Plectocarpon lichenum, Polycauliona stellata, Porpidia flavicunda, Pseudosagedia chlorotica, Rhizocarpon eupetraeoides, Rostania ceranisca, Sclerophora farinacea, Scytinium schraderi, Solorina bispora, Sphaerellothecium minutum, Sticta beauvoisii, S. fuliginosa, Tetramelas papillatus, Tremella cetrariicola, Umbilicaria lyngei, Usnea ceratina, Xanthomendoza fulva and Xylographa opegraphella. Details on additional rare or otherwise rarely collected species new to explored counties and districts are also provided. These include: Acarospora bullata, Ahtiana aurescens, Amygdalaria panaeola, Anaptychia crinalis, Arctoparmelia incurva, Arthonia diffusella, Baeomyces carneus, Blastenia ferruginea, Buellia badia, Calicium abietinum, Caloplaca saxicola, Cetraria aculeata, Chaenotheca stemonea, Chaenothecopsis perforata, Cliostomum griffithii, Cyphobasidium hypogymniicola, Dermatocarpon dolomiticum, Dibaeis baeomyces, Flavocetraria nivalis, Fuscopannaria leucosticta, Heppia adglutinata, Heterodermia hypoleuca, H. obscurata, Hyperphyscia syncolla, Hypogymnia vittata, Immersaria athroocarpa, Inoderma byssaceum, Lecanora epanora, Lepraria cryophila, Leproplaca chrysodeta, Leptogium rivulare, Lichenodiplis lecanorae, Lichenostigma cosmopolites, Lithothelium hyalosporum, Lobaria scrobiculata, Lobothallia alphoplaca, Lopadium disciforme, Melanelixia albertana, M. subargentifera, Melanohalea halei, M. subolivacea, Muellerella erratica, Mycoblastus alpinus, Mycoglaena myricae, Myelochroa obsessa, Ovicuculispora parmeliae, Pannaria tavaresii, Parmotrema hypotropum, P. reticulatum, P. stuppeum, Peltigera venosa, Pertusaria superiana, Phacopsis oxyspora var. oxyspora, Physcia americana, Physcia tenella, Physconia grumosa, Placidium arboreum, Polychidium muscicola, Porina scabrida, Porpidia degelii, Pseudocyphellaria holarctica, Pseudoschismatomma rufescens, Psoroma hypnorum, Punctelia appalachensis, P. stictica, Rhizocarpon eupetraeum, Rinodina pachysperma, Sarea difformis, Scytinium gelatinosum, Scytinium intermedium, Sphaerophorus fragilis, S. globosus, Stictis radiata, Synalissa ramulosa, Syzygospora physciarcearum, Teloschistes chrysophthalmus, Thyrea confusa, Toninia aromatica, Tremella everniae, Umbilicaria arctica, U. hirsuta, U. proboscidea, U. torrefacta, Usnea glabrescens and Xanthoparmelia angustiphylla.
... Most collections of J. lactea in North America have been made in the eastern U.S. and Canada. However, although extensive surveys carried out in these regions have reported Julella fallaciosa (Arnold) R.C. Harris, none have turned up J. lactea (e.g., Lendemer & Noell 2018, Seaward et al. 2017, Wong & Brodo 1992, which suggests it is uncommon. Nevertheless, no attempt has been made to locate historical collections to ascertain if they are extant, which is necessary for a sound conservation assessement. ...
... Thelotrema subtile Tuck. also has transversely septate ascospores, occurs in the northeastern North America, and is similar in appearance, but it is distinguished by narrower ascospores (6-7 µm wide vs. 8-10 μm in T. suecicum) and the apothecia are less prominant (mostly immersed vs. raised and in warts in T. seucicum) (Brodo 1961, Frisch et al. 2006, Lendemer & Noell 2018, James 1977 NOTES. -Trapeliopsis gelatinosa is here reported for the first time from Prince Edward Island. ...
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Major range extensions for Canadian lichens and allied fungi are presented. Six species are reported for the first time from Canada: Chaenothecopsis lecanactidis, C. nigripunctata, Chrysothrix insulizans, Julella lactea, Parmotrema stuppeum, and Porina scabrida. New reports are made for the first time from six provinces and one territory: British Columbia (Bryoria furcellata, Chaenothecopsis lecanactidis, C. nigripunctata), New Brunswick (J. lactea), Nova Scotia (Bacidia polychroa, Chaenothecopsis tsugae, C. insulizans, Cladonia cryptochlorophaea, Diplotomma venustum, Herteliana schuyleriana, J. lactea, Lepraria hodkinsoniana, L. humida, L. oxybapha, Megalaria pulverea, Parmotrema stuppeum, Plectocarpon lichenum), Ontario (Chaenothecopsis consociata, P. stuppeum, Porina scabrida), Nunavut (Nephroma parile, Ochrolechia mahluensis), Prince Edward Island (Cladonia merochlorophaea, Lepraria eburnea, Physcia alnophila, Thelotrema suecicum, Trapeliopsis gelatinosa, Xylographa pallens) and Quebec (Japewia subaurifera). Parmelia fraudans is reported for the first time from southern Ontario, and five species are reported new to the Canadian Arctic Archipelago (B. furcellata, Icmadophila ericetorum, Parmeliopsis ambigua, P. hyperopta, Vulpicida pinastri).
... The name Loxospora pustulata (Brodo & W.L. Culb.) Egan was applied to a common and widespread pustulose-sorediate crustose species with thamnolic acid that occurs throughout eastern North America (Brodo and Culberson 1986;Lendemer and Noell 2018). The discovery of fertile material led to its being transferred to the genus Lepra Scop. ...
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Loxospora is a genus of crustose lichenLoxospora is a genus of crustose lichens containing 13 accepted species that can be separated into two groups, based on differences in secondary chemistry that correlate with differences in characters of the sexual reproductive structures (asci and ascospores). Molecular phylogenetic analyses recovered these groups as monophyletic and support their recognition as distinct genera that differ in phenotypic characters. Species containing 2’-O-methylperlatolic acid are transferred to the new genus, Chicitaea Guzow-Krzem., Kukwa & Lendemer and four new combinations are proposed: C. assateaguensis (Lendemer) Guzow-Krzem., Kukwa & Lendemer, C. confusa (Lendemer) Guzow-Krzem., Kukwa & Lendemer, C. cristinae (Guzow-Krzem., Łubek, Kubiak & Kukwa) Guzow-Krzem., Kukwa & Lendemer and C. lecanoriformis (Lumbsch, A.W. Archer & Elix) Guzow-Krzem., Kukwa & Lendemer. The remaining species produce thamnolic acid and represent Loxospora s.str. Haplotype analyses recovered sequences of L. elatina in two distinct groups, one corresponding to L. elatina s.str. and one to Pertusaria chloropolia, the latter being resurrected from synonymy of L. elatina and, thus, requiring the combination, L. chloropolia (Erichsen) Ptach-Styn, Guzow-Krzem., Tønsberg & Kukwa. Sequences of L. ochrophaea were found to be intermixed within the otherwise monophyletic L. elatina s.str. These two taxa, which differ in contrasting reproductive mode and overall geographic distributions, are maintained as distinct, pending further studies with additional molecular loci. Lectotypes are selected for Lecanora elatina, Pertusaria chloropolia and P. chloropolia f. cana. The latter is a synonym of Loxospora chloropolia. New primers for the amplification of mtSSU are also presented.s containing 13 accepted species
... We then found fertile specimens ( Figure 2) and initially assumed in the field that the apothecia were admixed from adjacent thalli of Catillaria nigroclavata or Catinaria atropurpurea (Schaer.) Vězda & Poelt, both of which frequently grow on the smooth bark of hardwoods in eastern North America (Lendemer et al. 2016;Lendemer and Noell 2018;Tripp and Lendemer 2020). Both of those species are however, esorediate. ...
Article
Catillaria fungoides is newly reported for North America based on collections from the temperate eastern United States. A detailed description based on North American material is provided, the distribution is mapped, and images are provided. The species is likely widespread but overlooked due to its inconspicuous appearance.
... It is most likely to be confused with Myleochroa aurulenta (Tuck.) Elix & Hale, which is much more common, and differs in having a lightly yellow pigmented medulla that lacks stictic acid, pustulose soralia, and a smooth upper surface that lacks scrobiculae (Lendemer & Noell 2018). NOTES. ...
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New provincial and territorial records for Canadian lichens and allied fungi are presented, many of which represent major range extensions. Crespoa crozalsiana is reported for the first time from Canada. New reports are made for the first time from five provinces and one territory: Newfoundland and Labrador (Geltingia associata on Ochrolechia), Nova Scotia (Abrothallus santessonii on Platismatia glauca, Mycocalicium albonigrum, Pertusaria superiana, Physcia thomsoniana, Ramboldia elabens), Nunavut (Hypogymnia apinnata, Tuckermanopsis subalpina), Ontario (Cladonia asahinae, C. kanewskii, Crespoa crozalsiana), Prince Edward Island (Lepraria caesiella, P. superiana), and Quebec (Chaenothecopsis exilis). Geltingia associata is also reported for the first time from the Canadian Low Arctic and Lecidella scabra is reported for the first time from mainland Nova Scotia.
... In general, timber harvests were more frequent and had occurred more recently at the mature pine-dominated sites (i.e., OCPi; Table 1). Although we did not set out to constrain the sample to a single Cladonia species, all individuals included in the study were identified as C. subtenuis (Abbayes) Mattick, which is widely distributed in the MACP and southeastern US (Lendemer and Noell 2018). While it was not difficult to find samples within the study areas that had a recent history of burning, the previously unburned sites did yield the highest proportional representation of samples in the largest size class at 39%, versus 14% and 13% at the once and twice burned sites, respectively (Table 2). ...
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Background Prescribed fire is increasingly used to accomplish management goals in fire-adapted systems, yet our understanding of effects on non-target organisms remains underdeveloped. Terricolous lichens in the genus Cladonia P. Browne, particularly cushion-forming reindeer lichens belonging to Cladonia subgenus Cladina Nyl., fit into this category, being characteristic of fire-adapted ecosystems, yet highly vulnerable to damage or consumption during burns. Moreover, inherently slow dispersal and growth rates raise questions about how to conserve these taxa in the context of fire-mediated restoration management. This research was undertaken to identify factors that contribute to Cladonia persistence within areas subject to repeated burning and involved tracking the fate of 228 spatially isolated individuals distributed across seven sites previously burned zero to two times. Site selection was determined by edaphic factors associated with a rare inland dune woodland community type known to support relatively high densities of Cladonia . Results Evaluated across all sites, the post-burn condition of Cladonia subtenuis (Abbayes) Mattick samples, categorized as intact (32%), fragmented (33%), or consumed (36%) individuals, approximated a uniform distribution. However, their status was highly variable at the different sites, where from 0 to 70% were assessed as intact and 11 to 60% consumed. Machine-learning statistical techniques were used to identify the factors most strongly associated with fire damage, drawing from variables describing the proximate fuel bed, growth substrate, and fire weather. The final descriptive model was dominated by variables characterizing the understory fuel matrix. Conclusions Areas with highly contiguous fuels dominated by pyrogenic pine needles were most likely to result in consumption of individual Cladonia, whereas those growing in areas with low fuel continuity or in areas dominated by hardwood litter were more likely to persist (intact or as fragments). Further, substrates including bare soil and moss mats afforded more protection than coarse woody debris or leaf litter in settings where fuels were both contiguous and highly flammable. Our findings describe the characteristics of within-site fire refugia, the abundance of which may be enhanced over time through restoration and maintenance treatments including thinning, promotion of mixed-species overstory composition, and periodic burning. Because lichens contribute to, and are considered reliable indicators of forest health, fire-based restoration management efforts will benefit from improved understanding of how these vulnerable organisms are able to persist.
... Of the 599 species identified, 42% (252 species) were found in five or fewer sites. The same trend was recovered in earlier studies of two subdivisions of the MACP Lendemer and Noell, 2018). The highest overall species richness was found in the Inland Swamp sites, however these ecosystems were the most sampled in terms of number of sites, of any ecosystem in the study area. ...
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The Mid-Atlantic Coastal Plain (MACP) is an ecoregion with high biodiversity that is under imminent threat from sea level rise and habitat loss. Previous studies have shown i) the area to be high in lichen biodiversity, including endemic species, ii) the most lichen species-rich sites are the most imperiled by sea-level rise, and iii) common, widespread lichens have lost significant suitable habitat and are projected to lose more due to sea-level rise. Despite this, the spatial distributions of rare species and the compositional dynamics of lichen communities has not previously been examined. Here, we evaluate the community composition of 599 lichen species in 215 sites across the MACP. We tested whether community similarity is correlated with spatial proximity or environmental conditions. We found that sites with similar environmental characteristics had similar species composition, after controlling for geographic distance. Inland swamps had the highest per-site average number of unique species (1.3) and the two coastal ecosystems, maritime forests and pocosin (a unique form of peatland vegetation), each had an average of nearly one unique species per site. Across the entire MACP, 42% of species were found at five or fewer sites and these were mostly at sites under high risk of being affected by sea level rise. While habitats and species throughout the MACP have been projected to be negatively affected by sea level rise, our results suggest that rare lichens face particularly acute threats. Lack of suitable habitat inland at higher elevations may necessitate intensive mitigation, including facilitated transplants of both lichens and their host trees.
... Given the small number of known occurrences of Hypotrachyna oprah, we suspect that species is rare throughout its range. However, it is possible that, despite its distinctive morphology and brightly fluorescent cortex, H. oprah has been overlooked in the field and confused with H. osseoalba which is much more common and widely distributed (Figure 3; Harris 1995, Lendemer and Noell 2018). ...
Article
Hypotrachyna oprah is described as new to science from collections made at locations in southeastern North America (Alabama, Florida, North Carolina). The species is considered rare and was potentially confused with H. osseoalba in the past. It differs from H. osseoalba in having capitate soralia and producing echinocarpic acid, together with related substances, in the medulla. The specific epithet was chosen to honor Dr. Oprah Winfrey for her performances, media presence, and generous philanthropy that have substantially improved humanity.
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Lecidea varians is among the most common and abundant bark-dwelling crustose lichens in temperate eastern North America. As presently delimited, it is highly variable, including chemical and morphological diversity well beyond that currently accepted for most lichen species. The generic placement of L. varians has also been questioned for decades. It has long been recognized as aberrant in Lecidea and Pyrrhospora, excluded from Lecidella, and more recently transferred to Traponora. Drawing from the results of extensive chemical, molecular phylogenetic and morphological studies, we show that L. varians and its relatives represent a previously unrecognized lineage within the speciose lichen family Lecanoraceae. The lineage appears to occupy an isolated position, distinct from the aforementioned genera, and is newly described as the genus Xanthosyne (typified by L. varians). The chemical and morphological variation within L. varians is mirrored by, but not entirely correlated with, considerable molecular diversity. A new taxonomy is proposed for L. varians and its relatives to serve as a framework for future studies. Three species are recognized: X. varians (≡ Lecidea varians), common and widespread in parts of North America; X. granularis, a new species from the Atlantic Coast of eastern North America that differs morphologically from X. varians in having a leprose thallus; and X. sharnoffiorum, a new species also found mainly along the Atlantic Coast of eastern North America, which has a coarsely granular, non-leprose thallus and produces a unique, unidentified xanthone. Multiple well-supported lineages were recovered within X. varians that correlate to varying degrees with chemical and morphological variability, as well as geographic distribution. Eight subspecies are recognized to accommodate the variation within X. varians: X. varians subsp. exigua comb. nov. (≡ Lecidea exigua) characterized by the presence of atranorin and a consistent set of three xanthones, is widespread in southern Europe and western North America (coastal California); X. varians subsp. varians (≡ Lecidea varians) is distributed mainly in northeastern North America and produces thuringione and arthothelin; X. varians subsp. morsei subsp. nov. is morphologically and chemically variable, with one chemotype (thiophanic acid) with a northeastern distribution, and the other with a unique and unidentified xanthone, found mainly in the interior U.S.A.; X. varians subsp. obscura subsp. nov. occurs mainly in the central U.S.A. and North Temperate regions, produces a unique, unidentified xanthone and generally has black apothecia with green epihymenial pigments; X. varians subsp. pseudomorsei subsp. nov. and X. varians subsp. submorsei subsp. nov. resemble X. varians subsp. morsei but differ in molecular sequence characters; X. varians subsp. subtilis comb. nov. (≡ Lecidea subtilis) and X. varians subsp. subexigua subsp. nov. occur in the Appalachian Mountains, the former producing atranorin and the latter lacking atranorin, both with thiophanic acid with or without other xanthones. In an addendum, Lecidella subviridis is discussed with respect to the genus Xanthosyne. An identification key is provided for all species and their subspecies within Xanthosyne.
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Arthonia frostiicola and A. galligena are described as new to science based on collections from mountainous regions of southeastern North America. Arthonia frostiicola infects the saxicolous lichen Dirinaria frostii, producing emarginate black apothecia which erupt from within the host thallus. It is characterized by a dark hypothecium and 1-septate, obovoid ascospores which turn brownish and verruculose in age. It is known from five collections made in the southern Appalachian Mountains and Ozark Mountains in southeastern North America. Arthonia galligena produces galls in the thallus and apothecia of the corticolous lichens Lecanora masana and L. rugosella, and is apparently endemic to the high elevations of the southern Appalachian Mountains. It is characterized by a variably pigmented, pale to red-brown hypothecium and 2-septate, macrocephalic ascospores which turn brownish and verruculose in age. Keys to the species of Arthonia on Caliciales and Lecanoraceae are provided.
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Lichens are known to be sensitive to changes in air quality. The recent closure of a coal-fired electric generating plant in New Jersey has set up a natural experiment to study the potential rebound of nearby lichen communities. The study area is the Abbott Marshlands, an ecologically important freshwater tidal wetland along the Delaware River, much of which is protected open space. To establish a baseline for future study, a biodiversity inventory of lichens and allied fungi was undertaken in the Abbott Marshlands, yielding 57 species.
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Since its resurrection, the resinicolous discomycete genus Sarea has been accepted as containing two species, one with black apothecia and pycnidia, and one with orange. We investigate this hypothesis using three ribosomal (nuITS, nuLSU, mtSSU) regions from and morphological examination of 70 specimens collected primarily in Europe and North America. The results of our analyses support separation of the traditional Sarea difformis s.l. and Sarea resinae s.l. into two distinct genera, Sarea and Zythia . Sarea as circumscribed is shown to comprise three phylospecies, with one corresponding to Sarea difformis s.s. and two, morphologically indistinguishable, corresponding to the newly combined Sarea coeloplata . Zythia is maintained as monotypic, containing only a genetically and morphologically variable Z. resinae . The new genus Atrozythia is erected for the new species A. klamathica . Arthrographis lignicola is placed in this genus on molecular grounds, expanding the concept of Sareomycetes by inclusion of a previously unknown type of anamorph. Dating analyses using additional marker regions indicate the emergence of the Sareomycetes was roughly concurrent with the diversification of the genus Pinus , suggesting that this group of fungi emerged to exploit the newly-available resinous ecological niche supplied by Pinus or another, extinct group of conifers. Our phylogeographic studies also permitted us to study the introductions of these fungi to areas where they are not native, including Antarctica, Cape Verde, and New Zealand and are consistent with historical hypotheses of introduction.
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The first checklist of lichenized, lichenicolous and lichen-allied fungi from the Kathy Stiles Freeland Bibb County Glades Preserve in Bibb County, Alabama, is presented. Collections made during the 2017 Tuckerman Workshop and additional records from herbaria and online sources are included. Two hundred and thirty-eight taxa in 115 genera are enumerated. Thirty taxa of lichenized, lichenicolous and lichen-allied fungi are newly reported for Alabama: Acarospora fuscata, A. novomexicana, Circinaria contorta, Constrictolumina cinchonae, Dermatocarpon dolomiticum, Didymocyrtis cladoniicola, Graphis anfractuosa, G. rimulosa, Hertelidea pseudobotryosa, Heterodermia pseudospeciosa, Lecania cuprea, Marchandiomyces lignicola, Minutoexcipula miniatoexcipula, Monoblastia rappii, Multiclavula mucida, Ochrolechia trochophora, Parmotrema subsumptum, Phaeographis brasiliensis, Phaeographis inusta, Piccolia nannaria, Placynthiella icmalea, Porina scabrida, Psora decipiens, Pyrenographa irregularis, Ramboldia blochiana, Thyrea confusa, Trichothelium americanum, Verrucaria calkinsiana, V. fayettensis, and Xanthocarpia feracissima. Protoblastenia ozarkana an undescribed species originally recognized from the Ozarks is also reported. This checklist serves as an important baseline for future studies of glade communities in Bibb County and, more generally, for calcareous glades across Alabama and throughout the southeastern United States.
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Candelariella xanthostigmoides is reported new to North America. The name is applied to what was previously referred to as C. reflexa in North America. The distributions of C. xanthostigmoides and the morphologically similar C. efflorescens in North America are reviewed. A lectotype is selected for Candelaria concolor var. effusa and the name is placed in synonymy with C. concolor.
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A preliminary treatment of the members of the genus Heterodermia occurring in eastern North America is provided. A key to species is included with color images of many species that have not been adequately illustrated previously. A new species, Heterodermia erecta, is described from high elevations of the southern Appalachians. Heterodermia microphylla is provisionally excluded from the study area as all specimens examined were misidentifications of other taxa. A norstictic acid deficient strain of H. neglecta is recognized pending further study of the material which may warrant recognition as a distinct species consisting of disjunct populations in the Canadian Maritimes, southern Appalachian Mountains, and central Florida.
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Notes on the discovery of several rare, reproductively atypical populations of Ochrolechia africana and O. arborea in eastern North America are presented. Sorediate fertile populations of the typically esorediate and fertile species O. africana were found in the Coastal Plain of southeastern North America. Conversely fertile sorediate populations of O. arborea, a species that is typically sterile and sorediate, were found in Maine and Pennsylvania, U.S.A. The unusual populations are described in detail and their geographic distributions mapped within the context of the reproductively typical populations of each species. A discussion of the labile nature of reproductive modes in Ochrolechia species is presented. The positive hypochlorite reaction in the amphithecial medulla and presence of 4,5-di-O-methylhiascic acid in the apothecia, together with the presence of lichexanthone in all tissues, point to a close relationship of O. arborea with O. mexicana.
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Two new species of Chrysothrix from eastern North America are described: C. chamaecyparicola to accommodate the North American populations previously referred to as C. flavovirens, and C. susquehannensis, the first species in the genus with lecanoric acid.
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The distinguishing features of Ropalospora viridis and Fuscidea pusilla are discussed. The geographic distributions of the two species in eastern North America are revised: although both species have an Appalachian-Great Lakes distribution they have somewhat differing biogeographic tendencies. Fuscidea pusilla is a rare species of the northern boreal forests with disjunct populations in the central Appalachian Mountains, whereas R. viridis is common and widespread throughout the Appalachian Mountains and their outliers with disjunct populations in the Great Lakes. Color illustrations of both species are provided.
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Version 21 of the checklist of lichen-forming, lichenicolous and allied fungi occurring in North America north of Mexico is presented. It includesa a total of 5,421 species in 733 genera, with an additional 41 subspecies, 45 varieties, and 3 forms. The total species number includes 588 lichenicolous fungi, 96 saprophytic fungi related to lichens or to lichenicolous fungi, and another 53 species of varying and/or uncertain biological status.
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Arthothelium lichenale is placed in synonymy with Mycoporum compositum. The morphological distinctions between Collema pustulatum and Leptogium apalachense are discussed and the North American distributions of the species are revised. The distribution of Lecidea roseotincta in North America is extended to include the central and southern Appalachian Mountains. The distribution of Lecidella subviridis is expanded in northeastern North America. Pyrenula reebiae is placed in synonymy with P. leucostoma and both species are illustrated and discussed. Pyrenula shirabeicola is removed from synonymy with P. pseudobufonia and both species are illustrated and discussed. The following taxa are newly reported from North America: Calvitimela cuprea (Canada, Newfoundland & Labrador), Hypotrachyna consimilis (U.S.A., North Carolina), Schismatomma graphidioides (U.S.A., Alabama and New Jersey).
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1. The species of Karschia s. lat. are taxonomically treated. 2. In a general part technical problems, the history of the genus, the characters used for the delimitation of the genera are discussed, a new ascus-type characteristic for Dactylospora is described and annotations to biology and distribution patterns are given. Essential results seem to be that all the species of the lecanoralean genera treated live together or close to algae and that the lichenicolous and parasitic species of Karschia s. lat. are specific to at least groups of hosts. 3. Keys to the genera with apothecial or pseudothecial fruiting bodies as well as to all species and varieties of Karschia s. lat. are given. 4. Sixty-eight species and varieties belonging to 20 different genera and 3 species, the generic position of which is not clear at this time, are treated. Four genera, 1 subgenus and rnany infrageneric taxa are recognized as synonyms. Six genera, 9 species and 5 varieties are described as new and 30 new combinations are proposed. 5. The species of Karschia s. lat. belong to the following 19 genera: Buellia, Epilichen, Rhizocarpon, Rinodina, Dactylospora, Buelliella, Colensoniella, Cycloschizon, Dothidea, Eutryblidiella, Gibbera, Heterosphaeriopsis, Karschia s. str., Poetschia, Pseudodiscus, Rhizodiscina, Rhizogene, Schrakia, and Stratisporella. 6. Line drawings, all are originals of the author, are added to many descriptions of accepted taxa. 7. Twenty-five not seen, doubtful or to be exduded taxa are listed. 8. Both an index of the hosts and an index of the species as well as infraspecific taxa are given.
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The cyanomorph and photosymbiodemes are here reported for the first time for Ricasolia virens (With.) H.H. Blom & Tønsberg comb. nov. (≡ Lobaria virens (With.) J.R. Laundon). The cyanomorph of R. virens is dendriscocauloid. The observed early developmental stages involve (1) a free-living cyanomorph and (2) a photosymbiodeme composed of the cyanomorph supporting small, foliose, chloromorphic lobes. Whereas the chloromorph continues to grow, the cyanomorph decays and disappears leading to the final stage (3), the free-living chloromorph. Secondary cyanomorphs emerging from the chloromorph are not known.
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The results of a large-scale biodiversity inventory of lichens (including lichenicolous and allied fungi) in the Dare Regional Biodiversity Hotspot (DRBH) are presented. The DRBH is a region within the Mid-Atlantic Coastal Plain (MACP) of eastern North America that was recently delineated based on its unique and diverse lichen communities relative to other areas of the Atlantic Coast. Drawing on 4,952 newly generated voucher specimens from 49 sites, patterns of biodiversity and biogeography are presented and discussed within the context of both the DRBH and the broader MACP. Relationships between natural communities, vegetation, and lichen communities are discussed, as are threats to the lichen biota. A series of conservation actions are presented together with avenues for future study. In addition, supplementary resources are provided in the form of: (a) a checklist of DRBH lichens, lichenicolous fungi, and allied fungi; (b) keys to DRBH lichens and lichenicolous and allied fungi; and (c) formal descriptions of the following species new to science that were discovered during the inventory: Albemarlea pamlicoensis gen. et. sp. nov., Arthonia agelastica sp. nov. (on Lecanora louisianae B. de Lesd.), Arthonia hodgesii sp. nov. (on Graphis lineola), Arthonia stevensoniana sp. nov. (on Haematomma accolens), Lichenochora haematommatum sp. nov. (on Haematomma persoonii), Megalaria alligatorensis sp. nov., Minutoexcipula miniatoexcipula sp. nov. (on Pertusaria epixantha), Trichosphaerella buckii sp. nov. (on Punctelia rudecta). **THIS ARTICLE IS OPEN ACCESS AND CAN BE DOWNLOADED DIRECTLY FROM THE JOURNAL WEBSITE ON BIOONE: http://www.bioone.org/doi/abs/10.2179/15-073R2 **
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The lichens of Prince Edward Island (PEI) are well known to have been inadequately sampled and not well understood. In this study, 19 biologically diverse forest remnants and other potentially rich localities were explored for their lichen vegetation, and 118 new county records and 71 species new for the province were discovered. Together with previously studied sites, 38 localities in total have now been surveyed. A new checklist based on these surveys was prepared for all the lichens of the island. In addition, conservation status (S-ranks) is proposed for 153 species of the 326 species in 118 genera now known for the province. Four species received a rank of S1 (critically imperiled): Anaptychia crinalis, Megaspora verrucosa, Pannaria lurida, and Sclerophora amabilis; and six species received a rank of S2 (imperiled): Acrocordia cavata, Bryoria salazinica, Heterodermia speciosa, Menegazzia terebrata, Pannaria rubiginosa, and Ramalina thrausta. The importance of baseline data for future conservation
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The first confirmed North American report of Acrocordia gemmata is presented. The first fertile collections of Heiomasia seaveyorum are documented and illustrated. The recent North American report of Lecanora barkmaniana is shown to be based on a misidentification of L. floridula. The following species are reported for the first time from North America: Ochrolechia isidiata (Georgia, U.S.A.) and Roselliniopsis tropica (Delaware, Maryland and North Carolina, U.S.A.; lichenicolous on Ochrolechia africana). The distinguishing features of Pertusaria obruta and P. sinusmexicani are discussed, the species are illustrated, and maps of the revised distributions are presented.
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The new genus Tuckermanella is described to accomodate the cetrarioid lichen species which have been referred to as the "Cetraria fendleri group," most of which have been placed more recently in the related genus Tuckermannopsis. New combinations are provided for the four previously described species, and two new species are described: Tuckermanella arizonica sp. nov. and T. pseudoweberi sp. nov.
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The effects of prescribed burning and thinning on lichen communities is a poorly understood aspect of biodiversity conservation, despite the widespread use of these practices to achieve conservation-oriented land management goals. To address this knowledge gap we documented apparent changes in the diversity and abundance of lichens following 0 to 2 growing-season burns preceded by 0 to 1 commercial thinnings within nine southern pine dominated stands on the Delmarva Peninsula of Maryland, USA. Corticolous lichens growing on the stems and within the canopies of pines and co-occurring hardwoods were identified to species and fractional coverage was estimated; growth forms and reproductive modes were also determined. A total of 93 lichen taxa were recorded on the 19 tree species (4 pines, 15 hardwoods) represented in this study. Burning emerged as a strong driver of reductions in lichen diversity (P = 0.002), whereas thinning in the absence of burning did not (P = 0.279). In general, we found that lichens growing on tree bases and lower bole sections were more strongly impacted by burning, both in terms of diversity and cover, than those residing in the canopy. The apparent refugia represented by the canopy was qualified by the limited overlap in lichen species composition observed among the various sampling heights. This work calls attention to an understudied component of biodiversity that appears to be sensitive to fire management; however, we suggest that these results need to be interpreted in the context of altered disturbance regimes and the trajectory of community assembly resulting from long-term fire exclusion.
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Physciella, a new genus in the lichen family Physciaceae, is described and compared to its closest relatives. A combination of characters, including its prosoplectenchymatous, pale lower cortex, its lack of atranorin in the upper cortex, and its short, ellipsoid conidia, distinguish it from Physcia and Phaeophyscia. Four species, Ph. chloantha, Ph. denigrata, Ph. melanchra, and Ph. nepalensis are currently placed in the new genus.
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An artificial group of 17 species of Caloplaca is treated for North and Central America. The group includes those species of the genus with brown or black apothecia and with a KOH- thallus and KOH- or KOH+ purplish epihymenium. The K+ purplish reaction is distinguished from the K+ red reaction in those species with parietin complex. A key for the species treated is presented along with diagnoses and distributions. Critical notes are given for many other species in this group from other parts of the world. Four new species are described: Caloplaca brunneola, C. dakotensis, C. neotropica, and C. parvula. New combinations are made for Caloplaca albovariegata, C. diphasia, and C. oblongula. Caloplaca conversa is reported for the first time from North America.
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A review of the crustose lichen genus Phlyctis in North America is presented derived from large-scale studies of chemical, morphological, and molecular data (ITS and mtSSU). Five species are recognized based on a combination of morphological and chemical characters, namely P. agelaea, P. argena, P. boliviensis, P. speirea and the newly described P. petraea. Analyses of molecular data supported the recognition of P. boliviensis and P. petraea but recovered P. agelaea, P. argena or P. speirea in a single clade with little internal phylogenetic structure, suggesting their circumscription based on reproductive mode and thallus morphology requires further study. An account is provided that includes an identification key, discussion of each species, distribution maps and illustrations of morphology. Phlyctis petraea, provisionally named more than a decade ago, is described as new to science. Molecular phylogenetic analyses using ITS and mtSSU sequence data both confirm the placement of P. petraea in Phlyctis and demonstrate two known chemotypes (one with norstictic acid and one with norstictic and stictic acids) are not reciprocally monophyletic and should be treated as variants of a single species. Psathyrophlyctis, described as a member of the Phlyctidaceae, is discussed and treated as a member of the Lecanorales incertae sedis.
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Recent collections from southeastern North America prompted a revision of Gyalideopsis ozarkensis and G. subaequatoriana. The protologues and original material of these names are shown to comprise elements of three seemingly allopatric taxa that can be recognized based on differences in diahyphae morphology that appear to be correlated to different biogeographic patterns. Gyalideopsis ozarkensis is restricted to specimens with long multi-septate diahyphae from the Ozarks, Ouachitas, and the southwestern Appalachian Mountains. Gyalideopsis subaequatoriana is restricted to collections from tropical central Florida with moniliform diahyphae. A third species, G. bartramiorum, is described as new to science for material from the Mid-Atlantic Coastal Plain and southern Appalachians Mountains. All three taxa are illustrated and maps of their geographic distributions are presented.
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A distinctive group of species historically classified within Pertusaria subgenus Pionospora have been treated at the genus level under the name Variolaria, and more recently Marfloraea. Recent work has shown that Lepra is the oldest available name for this group. A nomenclatural summary of the members of the group that occur in North America north of Mexico is presented, including formal new combinations for the epithets that have not already been transferred to Lepra (i.e., P. andersoniae, P. commutata, P. floridiana, P. hypothamnolica, P. multipunctoides, V. pustulata, P. subdactylina, P. trachythallina, P. ventosa and P. waghornei). A key to the species occurring in the region is also presented.
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National Forest lands in the state of Washington were surveyed for calicioid lichens and fungi. Sixty-four plots were investigated and 930 collections were made. Fifty-seven species in nine genera were found, including Chaenothecopsis lecanactidis, C. nivea, C. vainioana, and Phaeocalicium interruptum, which are reported as new to North America. Chaenothecopsis norstictica and C. nigra are reported as new to western North America. Our observations confirm conclusions drawn by others that forests with the highest structural diversity have the highest number of calicioid species present.
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The following corrections and amendments are made to the 2016 classification of lichenized fungi published in the previous issue of this journal. Four families are added: Harpidiaceae (Pezizomycotina incertae sedis), with the two genera Euopsis and Harpidium; Pleomassariaceae (Pleosporales), with the genus Splanchonema; Squamarinaceae (Lecanorales), with the two genera Herteliana (moved from Ramalinaceae) and Squamarina (moved from Stereocaulaceae); and Trichosphaeriaceae (Sordariomycetes: Trichosphaeriales), with the genus Cresporhaphis. The following previously overlooked genera are also added: Allophoron (Pezizomycotina incertae sedis), Cresporhaphis (Trichosphaeriaceae), Gabura (Arctomiaceae), Julella (Trypetheliaceae), Knightiella (Icmadophilaceae), Porpidinia (Lecideaceae), Protoroccella (Roccellaceae), Psoromidium (Pannariaceae) and Tremotylium (Arthoniales incertae sedis). The classification is adjusted for four genera: Asteroporum (moved from Pezizomycotina incertae sedis to Dothideomyce...
Article
Ascomata, ascus, spore anatomy, spore wall ornamentation, and conidiophore type are discussed with respect to the limits of the genus Amandinea Scheid. & Mayrh. Four new species combinations are made and eight taxa placed in synonymy. Amandinea dakotensis (H. Magn.) P. May & Sheard comb. nov. and A. milliaria (Tuck.) P. May & Sheard comb. nov. are transferred from the genus Rinodina (Ach.) Gray. Amandinea leucomela (Imshaug) P. May & Sheard comb. nov. and A. polyspora (Willey) E. Lay & P. May comb. nov. are transferred from Buellia De Not.
Article
Ninety years after Zahlbruckner, we present the most recent update to the classification of lichen fungi in the Ascomycota and Basidiomycota to genus level, with species numbers and references to changes compared to the 2010 Outline of Ascomycota and other recent classifications. Updated statistics on global species richness of lichen fungi and species richness at family, order and class level are given. The number of accepted species is 19,387 in 995 genera, 115 families, 39 orders and eight classes. Lichenized Basidiomycota amount to 172 species (0.9% of the total), 15 genera (1.5%), five families (4.3%), five orders (12.8%) and one class (12.5%). The most speciose genera are Xanthoparmelia, Lecanora, Arthonia, Cladonia, Pertusaria, Ocellularia, Graphis, Caloplaca, Usnea and Buellia. The average number of species per genus is 19.5 and 256 genera are monospecific. Using newly defined categories, two genera (Xanthoparmelia, Lecanora) are ultradiverse (more than 500 species), 17 hyperdiverse (201–500 species) and 12 megadiverse (101–200). The largest family is Parmeliaceae, with 2,765 species and 77 genera, followed by Graphidaceae (2,161; 79), Verrucariaceae (943; 43), Ramalinaceae (916; 43) and Lecanoraceae (791; 25). The largest order is Lecanorales, with 6,231 species and 234 genera, followed by Ostropales (3,261; 138), Arthoniales (1,541, 103), Peltigerales (1,301; 67) and Caliciales (1,276; 55). The largest class is Lecanoromycetes, with 15,131 species and 701 genera, followed by Arthoniomycetes (1,541; 103), Eurotiomycetes (1,203; 63), Dothideomycetes (812; 39) and Lichinomycetes (390; 50). A total of 751 out of 995 genera (75%) have molecular data. Fifty-nine genera remain in unresolved positions at the family, order or class level. The phylogenetic position of the 39 orders containing lichenized fungi suggests 20–30 independent lichenization events during the evolution of higher Fungi, 14–23 in the Ascomycota and 6–7 in the Basidiomycota. The following names are validated: Candelariomycetidae Miądl. et al. ex Timdal & M.Westb. subcl. nov., Cystocoleaceae Locq. ex Lücking, B.P.Hodk. & S.D.Leav. fam. nov, Letrouitineae Gaya & Lutzoni subordo nov., Rhizocarpales Miądl. & Lutzoni ordo nov. and Teloschistineae Gaya & Lutzoni subordo nov. Lectotypes are designated for Clathroporinopsis M.Choisy and Protoschistes M.Choisy, making both synonyms of Gyalecta Ach., and Stromatothelium Trevis., making it a synonym of Pyrenula Ach. Members of Cyphobasidiales, which are here interpreted as hyperlichenized fungi, as well as fossil lichen fungi, are added in additional classifications in two appendices.
Article
A revisionary synopsis is presented for the family Trypetheliaceae , based on a separately published phylogenetic analysis of a large number of species, morpho-anatomical and chemical study of extensive material, and revision of numerous type specimens. A total of 418 species is formally accepted in this synopsis, distributed among 15 genera as follows: Aptrootia (3), Architrypethelium (7), Astrothelium (242), Bathelium (16), Bogoriella (29), Constrictolumina (9), Dictyomeridium (7), Distothelia (3), Marcelaria (3), Nigrovothelium (2), Novomicrothelia (1), Polymeridium (50), Pseudopyrenula (20), Trypethelium (16), and Viridothelium (10). All accepted genera, including new genera described separately in this issue, are keyed out and briefly described and discussed, and keys are provided for all accepted species within each genus. Entries with full synonymy and brief descriptions, and in part also discussions, are provided for all accepted species, except those newly described elsewhere in this issue, which are cross-referenced in the corresponding keys. The description of the newly defined genera takes into account phylogeny in combination with morpho-anatomical features with the result that they are mostly recognizable by a combination of thallus, ascoma and ascospore features. Most species previously assigned to the genera Astrothelium , Campylothelium , Cryptothelium , and Trypethelium , based on a schematic concept of ascoma morphology and ascospore septation, are now included in a single genus, Astrothelium , with highly variable ascoma morphology and ascospore septation but invariably with astrothelioid ascospores (at least when young), that is diamond-shaped lumina, and a well-developed, corticate, usually olive-green thallus that often covers the ascomata. While the genera Aptrootia (large, brown, muriform ascospores), Architrypethelium (large, mostly 3-septate ascospores), and Pseudopyrenula (ecorticate, white thalli and astrothelioid ascospores) are maintained, Trypethelium is redefined to include species with raised, pseudostromatic ascomata and multiseptate ascospores with thin septa. The sister group of Trypethelium is the genus Marcelaria , with brightly coloured pseudostromata and muriform ascospores. Bathelium is now limited to species with strongly raised, fully exposed pseudostromata and septate to muriform ascospores with thin septa. Several genera are recognized for more basal lineages with mostly ecorticate, white thalli and solitary, exposed ascomata previously assigned to Arthopyrenia , Mycomicrothelia and Polymeridium , viz . Bogoriella , Constrictolumina , Dictyomeridium , and Novomicrothelia . In addition, separate genera are accepted for the Trypethelium tropicum ( Nigrovothelium ) and T. virens ( Viridothelium ) groups. In addition, a refined species concept resulting from phylogenetic studies is employed which pays particular attention to morphological features of the thallus and ascomata. Of a total of 526 names checked, 107 remain synonyms of accepted names and a further eight are newly excluded from the family. Based on these redispositions, the following 146 new combinations are proposed, including reinstatement of numerous names previously subsumed into synonymy: Architrypethelium columbianum (Nyl.) Aptroot & Lücking comb. nov., A. grande (Kremp.) Aptroot & Lücking comb. nov., Astrothelium aeneum (Eschw.) Aptroot & Lücking comb. nov., A. alboverrucum (Makhija & Patw.) Aptroot & Lücking comb. nov., A. amazonum (R. C. Harris) Aptroot & Lücking comb. nov., A. ambiguum (Malme) Aptroot & Lücking comb. nov., A. andamanicum (Makhija & Patw.) Aptroot comb. nov., A. annulare (Spreng.) Aptroot & Lücking comb. nov., A. aurantiacum (Makhija & Patw) Aptroot & Lücking comb. nov., A. auratum (R. C. Harris) Aptroot & Lücking comb. nov., A. aureomaculatum (Vain.) Aptroot & Lücking comb. nov., A. basilicum (Kremp.) Aptroot & Lücking comb. nov., A. bicolor (Taylor) Aptroot & Lücking comb. nov., A. buckii (R. C. Harris) Aptroot & Lücking comb. nov., A. calosporum (Müll. Arg.) Aptroot & Lücking comb. nov., A. cartilagineum (Fée) Aptroot & Lücking comb. nov., A. cecidiogenum (Aptroot & Lücking) Aptroot & Lücking comb. nov., A. ceratinum (Fée) Aptroot & Lücking comb. nov., A. chapadense (Malme) Aptroot & Lücking comb. nov., A. chrysoglyphum (Vain.) Aptroot & Lücking comb. nov., A. chrysostomum (Vain.) Aptroot & Lücking comb. nov., A. cinereorosellum (Kremp.) Aptroot & Lücking comb. nov., A. cinereum (Müll. Arg.) Aptroot & Lücking comb. et stat. nov., A. confluens (Müll. Arg.) Aptroot & Lücking comb. nov., A. consimile (Müll. Arg.) Aptroot & Lücking comb. nov., A. deforme (Fée) Aptroot & Lücking comb. nov., A. defossum (Müll. Arg.) Aptroot & Lücking comb. nov., A. degenerans (Vain.) Aptroot & Lücking comb. nov., A. dissimilum (Makhija & Patw.) Aptroot & Lücking comb. nov., A. effusum (Aptroot & Sipman) Aptroot & Lücking comb. nov., A. endochryseum (Vain.) Aptroot & Lücking comb. nov., A. exostemmatis (Müll. Arg.) Aptroot & Lücking comb. nov., A. feei (C. F. W. Meissn.) Aptroot & Lücking comb. nov., A. ferrugineum (Müll. Arg.) Aptroot & Lücking comb. nov., A. galligenum (Aptroot) Aptroot & Lücking comb. nov., A. gigantosporum (Müll. Arg.) Aptroot & Lücking comb. nov., A. indicum (Upreti & Ajay Singh) Aptroot & Lücking comb. nov., A. infossum (Nyl.) Aptroot & Lücking comb. nov., A. infuscatulum (Müll. Arg.) Aptroot & Lücking comb. nov., A. irregulare (Müll. Arg.) Aptroot & Lücking comb. nov., A. keralense (Upreti & Ajay Singh) Aptroot & Lücking comb. nov., A. kunzei (Fée) Aptroot & Lücking comb. nov., A. leioplacum (Müll. Arg.) Aptroot & Lücking comb. nov., A. lugescens (Nyl.) Aptroot & Lücking comb. nov., A. luridum (Zahlbr.) Aptroot & Lücking comb. nov., A. macrocarpum (Fée) Aptroot & Lücking comb. nov., A. macrosporum (Makhija & Patw.) Aptroot & Lücking comb. nov., A. marcidum (Fée) Aptroot & Lücking comb. nov., A. megaleium (Kremp.) Aptroot & Lücking comb. nov., A. megalophthalmum (Müll. Arg.) Aptroot & Lücking comb. nov., A. megalostomum (Vain.) Aptroot & Lücking comb. nov., A. megaspermum (Mont.) Aptroot & Lücking comb. nov., A. meiophorum (Nyl.) Aptroot & Lücking comb. nov., A. meristosporoides (P. M. McCarthy & Vongshew.) Aptroot & Lücking comb. nov., A. meristosporum (Mont. & Bosch) Aptroot & Lücking comb. nov., A. neogalbineum (R. C. Harris) Aptroot & Lücking comb. nov., A. nigratum (Müll. Arg.) Aptroot & Lücking comb. et stat. nov., A. nigrorufum (Makhija & Patw.) Aptroot & Lücking comb. nov., A. nitidiusculum (Nyl.) Aptroot & Lücking comb. nov., A. octosporum (Vain.) Aptroot & Lücking comb. nov., A. oligocarpum (Müll. Arg.) Aptroot & Lücking comb. nov., A. olivaceofuscum (Zenker) Aptroot & Lücking comb. nov., A. papillosum (P. M. McCarthy) Aptroot & Lücking comb. nov., A. papulosum (Nyl.) Aptroot & Lücking comb. nov., A. peranceps (Kremp.) Aptroot & Lücking comb. nov., A. phaeothelium (Nyl.) Aptroot & Lücking comb. nov., A. phlyctaenua (Fée) Aptroot & Lücking comb. nov., A. porosum (Ach.) Aptroot & Lücking comb. nov., A. praetervisum (Müll. Arg.) Aptroot & Lücking comb. nov., A. pseudoplatystomum (Makhija & Patw.) Aptroot & Lücking comb. nov., A. pseudovariatum (Upreti & Ajay Singh) Aptroot & Lücking comb. nov., A. puiggarii (Müll. Arg.) Aptroot & Lücking comb. nov., A. pulcherrimum (Fée) Aptroot & Lücking comb. nov., A. pupula (Ach.) Aptroot & Lücking comb. nov., A. purpurascens (Müll. Arg.) Aptroot & Lücking comb. nov., A. pustulatum (Vain.) Aptroot & Lücking comb. nov., A. rufescens (Müll. Arg.) Aptroot & Lücking comb. et stat. nov., A. sanguinarium (Malme) Aptroot & Lücking comb. nov., A. santessonii (Letr.-Gal.) Aptroot & Lücking comb. nov., A. saxicola (Malme) Aptroot & Lücking comb. nov., A. scoria (Fée) Aptroot & Lücking comb. nov., A. scorizum (Müll. Arg.) Aptroot & Lücking comb. nov., A. sierraleonense (C. W. Dodge) Aptroot & Lücking comb. nov., A. sikkimense (Makhija & Patw.) Aptroot & Lücking comb. nov., A. spectabile (Aptroot & Ferraro) Aptroot & Lücking comb. nov., A. sphaerioides (Mont.) Aptroot & Lücking comb. nov., A. stramineum (Malme) Aptroot & Lücking comb. nov., A. straminicolor (Nyl.) Aptroot & Lücking comb. nov., A. subcatervarium (Malme) Aptroot & Lücking comb. nov., A. subdiscretum (Nyl.) Aptroot & Lücking comb. nov., A. subdisjunctum (Müll. Arg.) Aptroot & Lücking comb. nov., A. subdissocians (Nyl. ex Vain.) Aptroot & Lücking comb. et stat. nov., A. superbum (Fr.) Aptroot & Lücking comb. nov., A. tenue (Aptroot) Aptroot & Lücking comb. nov., A. thelotremoides (Nyl.) Aptroot & Lücking comb. nov., A. trypethelizans (Nyl.) Aptroot & Lücking comb. nov., A. tuberculosum (Vain.) Aptroot & Lücking comb. nov., A. ubianense (Vain.) Aptroot & Lücking comb. nov., A. variatum (Nyl.) Aptroot & Lücking comb. nov., A. vezdae (Makhija & Patw.) Aptroot & Lücking comb. nov., Bathelium austroafricanum (Zahlbr.) Aptroot & Lücking comb. nov., B. nigroporum (Makhija & Patw.) Aptroot & Lücking comb. nov., Bogoriella alata (Groenh. ex Aptroot) Aptroot & Lücking comb. nov., B. annonacea (Müll. Arg.) Aptroot & Lücking comb. nov., B. apposita (Nyl.) Aptroot & Lücking comb. nov., B. captiosa (Kremp.) Aptroot & Lücking comb. nov., B. collospora (Vain.) Aptroot & Lücking comb. nov., B. confluens (Müll. Arg.) Aptroot & Lücking comb. nov., B. conothelena (Nyl.) Aptroot & Lücking comb. nov., B. decipiens (Müll. Arg.) Aptroot & Lücking comb. nov., B. exigua (Müll. Arg.) Aptroot & Lücking comb. nov., B. fumosula (Zahlbr.) Aptroot & Lücking comb. nov., B. hemisphaerica (Müll. Arg.) Aptroot & Lücking comb. nov., B. lateralis (Sipman) Aptroot & Lücking comb. nov., B. leuckertii (D. Hawksw. & J. C. David) Aptroot & Lücking comb. nov., B. macrocarpa (Komposch, Aptroot & Hafellner) Aptroot & Lücking comb. nov., B. megaspora (Aptroot & M. Cáceres) Aptroot & Lücking comb. nov., B. miculiformis (Nyl. ex Müll. Arg.) Aptroot & Lücking comb. nov., B. minutula (Zahlbr.) Aptroot & Lücking comb. nov., B. modesta (Müll. Arg.) Aptroot & Lücking comb. nov., B. nonensis (Stirt.) Aptroot & Lücking comb. nov., B. obovata (Stirt.) Aptroot & Lücking comb. nov., B. pachytheca (Sacc. & Syd.) Aptroot & Lücking comb. nov., B. punctata (Aptroot) Aptroot & Lücking comb. nov., B. queenslandica (Müll. Arg.) Aptroot & Lücking comb. nov., B. socialis (Zahlbr.) Aptroot & Lücking comb. nov., B. striguloides (Sérus. & Aptroot) Aptroot & Lücking comb. nov., B. subfallens (Müll. Arg.) Aptroot & Lücking comb. nov., B. thelena (Ach.) Aptroot & Lücking comb. nov., B. triangularis (Aptroot) Aptroot & Lücking comb. nov., B. xanthonica (Komposch, Aptroot & Hafellner) Aptroot & Lücking comb. nov., Constrictolumina esenbeckiana (Fée) Lücking, M. P. Nelsen & Aptroot comb. nov., C. leucostoma (Müll. Arg.) Lücking, M. P. Nelsen & Aptroot comb. nov., C. lyrata (R. C. Harris) Lücking, M. P. Nelsen & Aptroot comb. nov., C. majuscula (Nyl.) Lücking, M. P. Nelsen & Aptroot comb. nov., C. malaccitula (Nyl.) Lücking, M. P. Nelsen & Aptroot comb. nov., C. porospora (Vain.) Lücking, M. P. Nelsen & Aptroot comb. nov., Dictyomeridium amylosporum (Vain.) Aptroot, M. P. Nelsen & Lücking comb. nov., D. campylothelioides (Aptroot & Sipman) Aptroot, M. P. Nelsen & Lücking comb. nov., D. immersum (Aptroot, A. A. Menezes & M. Cáceres) Aptroot, M. P. Nelsen & Lücking comb. nov., D. isohypocrellinum (Xavier-Leite, M. Cáceres & Aptroot) Aptroot, M. P. Nelsen & Lücking comb. nov., D. paraproponens (Aptroot, M. Cáceres & E. L. Lima) Aptroot, M. P. Nelsen & Lücking comb. nov., Distothelia rubrostoma (Aptroot) Aptroot & Lücking comb. nov., Phyllobathelium chlorogastricum (Müll. Arg.) Aptroot & Lücking comb. nov., Pseudopyrenula cubana (Müll. Arg.) Aptroot & Lücking comb. nov., Viridothelium cinereoglaucescens (Vain.) Lücking, M. P. Nelsen & Aptroot comb. nov., V. indutum (Stirt.) Aptroot & Lücking comb. nov., and V. megaspermum (Makhija & Patw.) Aptroot & Lücking comb. nov. In addition, six replacement names are proposed: Astrothelium campylocartilagineum Aptroot & Lücking nom. nov., A. grossoides Aptroot & Lücking nom. nov., A. octosporoides Aptroot & Lücking nom. nov., A. scoriothelium Aptroot & Lücking nom. nov., A. pyrenastrosulphureum Aptroot & Lücking nom. nov., and Bathelium pruinolucens Aptroot & Lücking nom. et stat. nov. Along with this, 57 lectotypes are newly designated. Most species (392 out of 418) are illustrated, with a total of 697 images in 59 plates, including 406 type specimens. Where appropriate, taxa are briefly discussed. New country or continental records are listed for many species in their revised circumscription. A checklist of taxa described or placed in genera belonging in Trypetheliaceae but previously excluded from the family, and their current names, is also provided.
Article
Two species of Catinaria with an unusual hepaticolous (i.e. growing on liverworts) lifestyle are described as new to science. Catinaria brodoana is described from species of Cheilolejeunea sect. Leucolejeunea ( Lejeuneaceae ) growing in south-eastern North America . Catinaria radulae is described from Radula flavifolia ( Radulaceae ) growing in the Cape Horn Archipelago of southernmost Chile, South America. The species are compared with the type of Catinaria ( C. atropurpurea ). In addition to occurring on hepatics, C. brodoana is characterized by its cellular exciple, warted ascospores and thallus composed of goniocysts, while C. radulae is characterized by its exciple of radiating hyphae, warted ascospores and absence of a lichenized thallus.
Article
Preliminary, large-scale assessments of global sea-level rise (SLR) have predicted significant impacts to coastal and island biodiversity. Region-specific estimates of SLR impacts that incorporate accurate species distributions and local rates of SLR are now required for effective conservation planning. Here we use a dataset of > 13,000 occurrence records for lichens, obligate symbiotic fungi, in the Mid-Atlantic Coastal Plain of eastern North America to model distributions of 193 species. The resulting models were used to quantify the amount of each species' distribution that is occupied by unsuitable land use types, along with the potential area that will be lost to SLR. We show that species have likely already lost an average of 32% of their distributional area to development and agriculture, and are predicted to lose an average of 12.4 and 33.7% of their distributional area with one foot (~ 0.3 m) and six feet (~ 1.8 m) of SLR, respectively. Functional and taxonomic groups were compared to identify specific effects of SLR. We show that species reproducing with symbiotic propagules have significantly larger distributions than species that reproduce sexually with fungal spores alone, and that the sexually reproducing species are predicted to lose greater distributional area to SLR. Cladonia species occupy significantly less area in the MACP than Parmotrema species and are predicted to lose more of their distributions to SLR. We further examined patterns of total species diversity and found that the area with the highest diversity is the Dare Peninsula in North Carolina, which is also predicted to lose the most land area to SLR. The workflow established here is flexible and applicable to estimating SLR impacts worldwide and can provide essential insights for local conservation planning.
Article
Bacidia schweinitzii is a common crustose lichen that is widespread in eastern North America. It is comprised of three distinct morphotypes differing in apothecial pigmentation. Here we show that molecular data from the mtSSU region affirms the distinctiveness of these morphotypes, prompting the recognition of three species: B. schweinitzii s.str., B. ekmaniana sp. nov. and B. purpurans sp. nov. We also show that a common sorediate crustose lichen, sympatric with B. schweinitzii, represents a monophyletic lineage whose relationship with B. schweinitzii s.str. could not be resolved with certainty using analyses of ITS and mtSSU sequence data. We recognize this sorediate lineage as a distinct species, B. sorediata sp. nov. All four taxa are described, illustrated and mapped.
Article
Species delimitation in foliose macrolichens has long been dominated by chemotaxonomy, resulting in many examples of seemingly morphologically identical species that differ only in the secondary metabolites they produce. This study examines two such species that are widespread in southeastern North America: Parmotrema madagascariaceum (Hue) Hale and Parmotrema xanthinum (Müll. Arg.) Hale. Drawing on data from biogeography, chemistry, morphology, and molecular phylogenetic analyses of nuclear ribosomal internal transcribed spacer sequence data, the two species are treated as conspecific. A taxonomic treatment is presented along with a discussion of previous studies that have examined the delimitation of species that differ only in the presence or absence of compounds that are accessories in addition to a primary set of substances present in both species.
Article
An intensive lichen biodiversity inventory of the imperiled Mid-Atlantic Coastal Plain of eastern North America resulted in the discovery of a new species of the ecologically sensitive macrolichen genus Sticta. The species is formally described as S. deyana based on a combination of molecular and morphological data. It is most similar to the southern Appalachian endemic S. fragilinata, differing in its diminutive thallus, narrower lobes, and allopatric distribution. All but one population of S. deyana occurs within the Dare Regional Biodiversity Hotspot of coastal North Carolina and within the most conservative estimated sea-level rise by 2100.
Article
The genera Parmeliopsis and Imshaugia are reviewed for eastern North America, and descriptions, keys, distribution maps, and illustrations are provided for the 6 species recognized: P. ambigua, capitata, hyperopta, subambigua, I. aleurites, and I. placorodia. The recently minimally validated species, P. capitata R. C. Harris, is provided with a complete description and is found to differ from P. ambigua in its much higher frequency of capitate soralia, as well as 10 other characters, including its generally lighter colored lower surface, narrower, more ascending and more divergent lobes, smaller size of thalli which possess soralia, and less northerly geographical distribution. P. hyperopta, in addition to its well known color difference from P. ambigua and capitata, appears also to differ from them in its broader geographical distribution, soralia commonly both laminai and terminal, and its generally longer spores. P. subambigua differs from the other three species in Parmeliopsis in its non-overlapping geographical distribution and its diffuse, pustulate soralia. The geographical distribution of the two very distinctive species of Imshaugia are both found to be broader than previously reported.
Article
The synonymy and distribution of Pertusaria velata (Turner) Nyl. is reported and discussed.
Article
Discovery of a new species of Trapelia and one of Ainoa prompted a taxonomic revision of saxicolous, esorediate members of the genera Ainoa and Trapelia that occur in North America north of Mexico. In addition to the description of A. bella and T. stipitata, both from eastern North America, revised descriptions and distributions are presented for T. coarctata and T. glebulosa. All of the species are illustrated, and A. mooreana (syn. T. mooreana) is excluded from the North American checklist. © 2015 by The American Bryological and Lichenological Society, Inc.
Article
Fourteen Native American shell-middens were discovered on the Delmarva Peninsula in Kent, Queen Anne’s and Dorchester Counties, Maryland. Occupying these shell-middens is a unique and globally rare plant community that supports 202 native species and varieties of vascular plants, including 87 that are rare or uncommon on the Peninsula and 21 that are new additions to the flora of the Delmarva.