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Ten new species of corticolous pyrenocarpous lichens from NE Brazil

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Ten corticolous pyrenocarpous lichens are newly described from different forest biomes in NE Brazil. All were collected in the past two years in Atlantic rain forest or Caatinga vegetation in Pernambuco or Sergipe. The following species are described: Anisomeridium globosum, Pyrenula abditicarpa, P. albonigra, P. aurantiacorubra, P. celaticarpa, P. cinnabarina, P. inspersicollaris, P. musaespora, P. rubrolateralis, and Thelenella lateralis.
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Phytotaxa 197 (3): 197–206
www.mapress.com/phytotaxa/
Copyright © 2015 Magnolia Press Article PHYTOTAXA
ISSN 1179-3155 (print edition)
ISSN 1179-3163 (online edition)
Accepted by Thorsten Lumbsch: 31 Dec. 2014; published: 16 Feb. 2015
http://dx.doi.org/10.11646/phytotaxa.197.3.3
197
Ten new species of corticolous pyrenocarpous lichens from NE Brazil
ANDRÉ APTROOT1, DANNYELLY SANTOS ANDRADE2, CLÉVERTON MENDONÇA2, EDVANEIDE
LEANDRO DE LIMA4 & MARCELA EUGENIA DA SILVA CÁCERES2, 3
1ABL Herbarium, G.v.d.Veenstraat 107, NL-3762 XK Soest, The Netherlands; email: andreaptroot@gmail.com
2Programa de Pós-Graduação em Ecologia e Conservação, Universidade Federal de Sergipe, CEP: 49100-000, São Cristóvão, Sergipe,
Brazil.
3Departamento de Biociências, Universidade Federal de Sergipe, CEP: 49500-000, Itabaiana, Sergipe, Brazil;
email: mscaceres@hotmail.com
4Departamento de Micologia, Universidade Federal de Pernambuco, CEP: 50670-901, Recife, Pernambuco, Brazil;
email: edvaneidell@hotmail.com
Abstract
Ten corticolous pyrenocarpous lichens are newly described from different forest biomes in NE Brazil. All were collected
in the past two years in Atlantic rain forest or Caatinga vegetation in Pernambuco or Sergipe. The following species are de-
scribed: Anisomeridium globosum, Pyrenula abditicarpa, P. albonigra, P. aurantiacorubra, P. celaticarpa, P. cinnabarina,
P. inspersicollaris, P. musaespora, P. rubrolateralis, and Thelenella lateralis.
Keywords: Atlantic rain forest, Anisomeridium, Caatinga, Pernambuco, Pyrenula, Sergipe, Thelenella
Introduction
In tropical forests, pyrenocarpous lichens are one of the dominant lichen groups, together with Ostropales and
Arthoniales. The forests of equatorial Brazil are exceptionally rich in corticolous pyrenocarpous species. Following
a recent surge in collecting activity, many new species have been published in the last two years (Aptroot et al. 2012;
Aptroot et al. 2013; Cáceres et al. 2013; Lima et al. 2013; Aptroot et al. 2014).
The renewed interest in pyrenocarpous lichens is partly a result of the many ecological studies carried out recently
for various Master’s dissertations in Northeastern Brazil, under the guidance of the last author, where every different li-
chen species on each investigated tree should be collected and ultimately named. It also helps that a world key (Aptroot
2012) was published for the largest genus, Pyrenula Ach. (Acharius 1814: 117). Still, numerous additional new species
were found in the past years, including yet more Pyrenula species and a variety of other pyrenocarpous lichens.
The purpose of this paper is to formally describe these new species, which names can subsequently be used in
ecological studies, but also serves to describe the biodiversity in different forest biomes in Brazil. The present paper
describes species found in Atlantic rain forests or in Caatinga. At the moment, most of the species described here are
only known from one specimen or locality. However, they are generally morphologically well characterized. There is
no doubt that most will be found on other locations, once they are described. Many of the species that were described
by us in the past two years from Brazil have already been found more often; several of them also in other states.
Even some species described from Rondônia, in the Brazilian Amazon, have been found in Sergipe and/or Pernam-
buco, which are areas thousands of kilometers apart and with a different vegetation, within one year after they were
described; some were even already found in other countries. Some of these species turned out to be locally common
and dozens of specimens are now known. The actual description actually facilitates their subsequent recognition in
other studies and is a strong argument in favour of describing characteristic species even though only one specimen
is known. Details about undescribed species are usually only known to one or a few people and accumulation of such
information until more specimens are known from every species is contra-productive.
APTROOT ET AL.
198 Phytotaxa 197 (3) © 2015 Magnolia Press
Material and methods
Identification and descriptive work was carried out in Itabaiana, Universidade Federal de Sergipe, using a Leica EZ4
stereomicroscope and a Leica DM500 compound microscope, and also in Soest using an Olympus SZX7 stereomicroscope
and an Olympus BX50 compound microscope with interference contrast, connected to a Nikon Coolpix digital camera.
Sections were mounted in tap water, in which also all measurements were taken. Most specimens from this study are
mostly preserved in ISE, with duplicates in ABL. The chemistry of the type specimens was investigated by thin layer
chromatography (TLC) using solvent A (Orange et al. 2001).
The species
Anisomeridium globosum Aptroot, D.S. Andrade & M. Cáceres, sp. nov. (Fig. 1A–B)
Mycobank #811016
Corticolous Anisomeridium with thallus corticate, greyish green, ascospores 1-septate, 8–10.5 × 4.5–6 μm, septum distinctly submedian
so that the lumen of the lower cell is only about a quarter of the size from the upper cell.
Holotype:—BRAZIL. Sergipe: Capela, Refúgio de Vida Silvestre Mata do Junco; 10˚32’S, 37˚03’W; alt. 150 m; on
bark of tree; 11 February 2014, D.S. Andrade T2A20 (ISE; isotype: ABL).
Thallus thin, corticate, greyish green, shiny, surrounded by an irregular, c. 1 mm wide white prothallus zone. As-
comata almost globose, superficial in the bark but completely covered by a thin layer of thallus, 0.3–0.45 mm diam.,
single. Wall carbonized all around. Ostiole apical, black, protruding through the thallus. Hamathecium not inspersed
with oil droplets, filaments anastomosing above the asci. Asci cylindrical, 80–95 × 5.5–7.5 μm, with small ocular
chamber. Ascospores 8/ascus, hyaline, uniseriate, 1-septate, 8–10.5 × 4.5–6 μm, lower end pointed, upper end rounded,
septum distinctly submedian so that the lumen of the lower cell is only about a quarter of the size from the upper cell.
Pycnidia not observed. Chemistry: Thallus UV–; no substances detected with TLC.
Ecology and distribution:—On smooth bark in undisturbed Atlantic rain forest. Only known from Brazil.
Discussion:—In this genus there are only relatively few species known with a corticate thallus (Harris 1995;
Aptroot et al. 1997; Aptroot & Seaward 1999), and all have larger ascospores, and also differ in at least one other key
character.
FIGURE 1. Anisomeridium globosum (isotype ABL); A, habitus showing superficial ascomata; B, ascus. A: bar = 0.5 mm; B: bar = 10 μm.
PYRENOCARPOUS LICHENS Phytotaxa 197 (3) © 2015 Magnolia Press 199
Pyrenula abditicarpa Aptroot & M. Cáceres, sp. nov. (Fig. 2A–B)
Mycobank #811017
Pyrenula with the ascomata 1–2 mm deep immersed in the bark underneath the thallus, ascospores distoseptate muriform, 7–9 × 3–7-
septate, 50–55 × 23–25 μm.
Holotype:—BRAZIL. Sergipe: Areia Branca, Parque Nacional Serra de Itabaiana; 10˚45’37”S, 37˚22’15”W; alt. c.
250 m; on bark of tree; 18 September 2013, M.E.S. Cáceres & A. Aptroot 18593 (ISE; isotype: ABL).
Thallus thin, corticate, olive brown, smooth, closely following the rough bark, without pseudocyphellae, without
prothallus. Ascomata 1–2 mm deep immersed in the bark underneath the thallus, pyriform, 0.6–0.8 mm diam., single.
Wall carbonized all around. Ostiole apical, pale brown, depressed. Hamathecium not inspersed with oil droplets. As-
cospores 8/ascus, irregularly biseriate, brown, distoseptate muriform, 7–9 × 3–7-septate, 50–55 × 23–25 μm, lumina
mostly rounded. Pycnidia not observed. Chemistry: Thallus UV–; no substances detected with TLC.
Ecology and distribution:—On smooth bark in undisturbed Atlantic rain forest. Only known from Brazil.
Discussion:—This species is characterized by the deeply immersed ascomata and the mid-sized muriform as-
cospores. It would key out in couplet 48 in key A in the world key (Aptroot 2012: 16).
FIGURE. 2. Pyrenula abditicarpa (isotype ABL); A, habitus showing depressed ostioles; B, ascospores; C–D, P. albonigra (isotype
ABL); C, habitus showing ascomata covered by thallus except for a wide black spot around the ostiole; D, ascospores. A & C: bar = 0.5
mm; B: bar = 20 μm; D: bar = 5 μm.
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200 Phytotaxa 197 (3) © 2015 Magnolia Press
FIGURE 3 Pyrenula aurantiacorubra; A, field picture of a tree covered with the species in the field; B, ascospores showing the variation in size
even within a single ascus (isotype ABL); C, habitus showing brown, raised ascomata (isotype ABL); D–F, P. cinnabarina (isotype ABL); D, twig
covered with the species; E, habitus showing aggregated ascomata; F, ascospore. C & E: bar = 0.5 mm; D: bar = 1 cm; B & F: bar = 10 μm.
PYRENOCARPOUS LICHENS Phytotaxa 197 (3) © 2015 Magnolia Press 201
Pyrenula albonigra Aptroot, D.S. Andrade & M. Cáceres, sp. nov. (Fig. 2C–D)
Mycobank #811018
Pyrenula with pale grey corticate thallus which also covers the ascomata except for a wide black ostiole, ascospores 3-septate, 17–20 ×
7–9 μm.
Holotype:—BRAZIL. Sergipe: Capela, Refúgio de Vida Silvestre Mata do Junco; 10˚32’S, 37˚03’W; alt. 150 m; on
bark of tree; 11 February 2014, D.S. Andrade T2A27 (ISE; isotype: ABL).
Thallus thin, corticate, mineral grey, somewhat glossy, without pseudocyphellae, surrounded by an up to 1 mm
wide black prothallus line. Ascomata superficial, hemispherical, 0.3–0.4 mm diam., single, covered by the thallus
except for a wide black spot around the ostiole. Wall carbonized all around. Ostiole apical, black. Hamathecium not
inspersed with oil droplets. Ascospores 8/ascus, brown, irregularly biseriate, 3-septate, 17–20 × 7–9 μm, lumina dia-
mond-shaped, separated from the wall by a thick layer of endospore. Pycnidia not observed. Chemistry: Thallus UV–;
no substances detected with TLC.
Ecology and distribution:—On smooth bark in undisturbed Atlantic rain forest. Only known from Brazil.
Discussion:—This species is characterized by the pale grey corticate thallus which also covers the ascomata ex-
cept for a strongly contrasting wide black spot around the ostiole.
Pyrenula aurantiacorubra Aptroot & M. Cáceres, sp. nov. (Fig. 3A–C)
Mycobank #811019
Pyrenula with orange red thallus, ascospores muriform, 3(–5) × 1–2-septate, 9–18 × 5–10 μm.
Holotype:—BRAZIL. Sergipe: Ribeirópolis, Serra do Machado; 10˚33’S, 37˚22’W; alt. c. 250 m; on bark of tree; 9
May 2014, M.E.S. Cáceres & A. Aptroot 21677 (ISE; isotype: ABL).
Thallus thin, somewhat granular, orange red mottled with some grey, without pseudocyphellae, without proth-
allus. Ascomata superficial, globose, 0.2–0.35 mm diam., single, distinctly brown, generally with orange with red
pruina. Wall barely carbonized. Ostiole apical, black. Hamathecium not inspersed. Ascospores 8/ascus, brown, ir-
regularly biseriate, muriform, 3(–5) × 1–2-septate, 9–18 × 5–10 μm, lumina mostly rounded. Pycnidia not observed.
Chemistry: Pigment K+ deep crimson, UV+ orange. TLC revealed several anthraquinones including 7-chloroemodin
as major compound, and one or more derivatives of it as minor compounds; the lower part of the TLC plate is streaked
with purple until as high as Rf 4.
Ecology and distribution:—On smooth bark in disturbed Atlantic rain forest. So far only known from Brazil.
Discussion:—This species is internally very similar to Pyrenula ochraceoflava (Nyl.) R.C. Harris (1989: 96). For
instance, it also shows a large variation in ascospore size, even within one ascus. However, its thallus is spectacularly
red orange, and it was already recognized in the field (fig. 3A) as a species new to science, which is no often possible.
Pyrenula ochraceoflava grows at the same location (collecting numbers 2149 & 21654), and clearly differs by the yel-
low orange thallus. These two species were co-chromatographed and P. ochraceoflava contains only 7-chloroemodin
as major compound, and one or more derivatives of it as minor compounds; no further anthraquinones. The purple
streak is never formed on the TLC plate.
Pyrenula celaticarpa Aptroot & M. Cáceres, sp. nov. (Fig. 4A–C)
Mycobank #811020
Pyrenula with deeply immersed ascomata with red ostioles, ascospores 3-septate, 21–24 × 10–11 μm.
Holotype:—BRAZIL. Sergipe: Areia Branca, Parque Nacional Serra de Itabaiana; 10˚45’37”S, 37˚22’15”W; alt. c.
250 m; on bark of tree; 18 September 2013, M.E.S. Cáceres & A. Aptroot 18593 (ISE; isotype: ABL).
Thallus rather thick (0.1–0.2 mm thick), corticate, olive green, minutely cracked throughout, without pseudo-
cyphellae, without prothallus. Ascomata 1–2 mm deep immersed in the bark underneath the thallus, pyriform, 0.6–0.9
mm diam., single. Wall carbonized all around. Ostiole apical, usually red brown to red, rarely pale brown or almost
black, flush to distinctly convex. Hamathecium inspersed with hyaline oil droplets. Ascospores 8/ascus, irregularly
biseriate, dark brown, 3-septate, 21–24 × 10–11 μm, lumina diamond-shaped, separated from the wall by a thick layer
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of endospore, ends pointed, often slightly constricted at the septa. Pycnidia not observed. Chemistry: Ostiole K+ crim-
son, with unidentified anthraquinone (too little for TLC); thallus UV–, K+ orange brown, possibly due to traces of the
same anthraquinone.
Ecology and distribution:—On smooth bark in undisturbed Atlantic rain forest. Only known from Brazil.
FIGURE. 4. Pyrenula celaticarpa (isotype ABL); A, habitus showing convex, dark red to almost black ostioles; B–C, ascospores; D–E,
P. inspersicollaris (isotype ABL); D, ascospore; E, habitus showing a raised shared ostiole surrounded by immersed ascomata;. A, E: bar
= 0.5 mm; B: bar = 10 μm; C–D: bar = 5 μm.
Discussion:—This species is characterized by deeply immersed ascomata which are only visible by the ostioles,
which are bronw and convex when well developed. The orange brown reaction of the thallus is also unusual, although
positive K-reactions are present in more species, especially anthrquinone-containing species of the group around the
PYRENOCARPOUS LICHENS Phytotaxa 197 (3) © 2015 Magnolia Press 203
type species, Pyrenula nitida (Weigel) Ach. (Acharius 1814: 125). There are so far only two other Pyrenula species
described with ostioles that contain anthraquinones, viz. P. rubrostoma R.C. Harris (Tucker & Harris 1980: 16) and
P. rubrostigma Aptroot & M. Cáceres (Aptroot et al. 2013: 190); both species have superficial, conical ascomata.
Pyrenula celaticarpa is closest to an undescribed species collected in Puerto Rico, which mainly differs by the absence
of inspersion and somewhat larger ascospores.
Pyrenula cinnabarina Aptroot, E.L. Lima & M. Cáceres, sp. nov. (Fig. 3D–F)
Mycobank #811021
Pyrenula with thallus dark carmine red, ascomata 5–30 fused sideways, hamathecium not inspersed, ascospores 3-septate, 12–15 × 6–7 μm.
Holotype:—BRAZIL. Pernambuco: Buíque, Parque Nacional Vale do Catimbau; alt. c. 880 m; on bark of tree;
August 2012, E.L. Lima 01794 (URM 86516; isotype: ABL).
Thallus thin, surface granular, dark carmine red, without pseudocyphellae, without prothallus. Ascomata superfi-
cial, globose, 0.2–0.35 mm diam., in groups of 5–30 fused sideways with clearly fused walls but with separate ostioles,
completely covered by thallus. Wall carbonized all around. Ostiole apical, pale, nearly whitish. Hamathecium not in-
spersed with oil droplets. Ascospores 8/ascus, brown, uniseriate, 3-septate, 12–15 × 6–7 μm, lumina mostly diamond-
shaped, separated from the wall by a thick layer of endospore. Pycnidia not observed. Chemistry: Thallus K+ crimson,
UV+ orange; TLC revealed an anthraquinone with pink colour at Rf 2.
Ecology and distribution:—On smooth bark in undisturbed Caatinga forest. Only known from Brazil.
Discussion:—This bright red species is very conspicuous already in the field. The type collection contins of few
branches that are fully covered by this species. It is close to Pyrenula reginae E.L. Lima, Aptroot & M. Cáceres (Lima
et al. 2013: 199), which grows in the same area, and mainly differs by the inspersed hamathecium.
Pyrenula inspersicollaris Aptroot & M. Cáceres, sp. nov. (Fig. 4D–E)
Mycobank #811022
Pyrenula similar to P. septicollaris, but differing by the inspersed hamathecium, ascospores 3-septate, 17–20 × 5.5–6.5 μm.
Holotype:—BRAZIL. Sergipe: Areia Branca, Parque Nacional Serra de Itabaiana, S slope; 10˚44’35”S, 37˚20’25”W;
alt. c. 400 m; on bark of tree; 10 May 2014, M.E.S. Cáceres & A. Aptroot 21754 (ISE; isotype: ABL).
Thallus thin, corticate, dark brown, somewhat glossy, without pseudocyphellae, without prothallus. Ascomata
emergent from the bark but fully covered by thallus, pyriform, 0.3–0.5 mm diam., usually 2–7 fused, without clearly
fused walls but with fused ostioles. Wall carbonized all around. Ostiole lateral. Hamathecium inspersed with hyaline
oil droplets. Ascospores 8/ascus, brown, irregularly biseriate, 3-septate, 17–20 × 5.5–6.5 μm, lumina mostly rounded,
separated from the wall by a thick layer of endospore. Pycnidia not observed. Chemistry: Thallus UV–; no substances
detected with TLC.
Ecology and distribution:—On smooth bark in undisturbed Atlantic rain forest. Only known from Brazil.
Discussion:—This species is close to the common pantropical species Pyrenula septicollaris (Eschw.) R.C. Har-
ris (1989: 101), which also grows in the same location, in most characters, but differs by the inspersed hamathecium.
Additional specimen examined:BRAZIL. Sergipe: Parque Nacional Serra de Itabaiana, S slope; 10˚44’35”S,
37˚20’25”W; alt. c. 400 m; on bark of tree; 10 May 2014, M.E.S. Cáceres & A. Aptroot 21788 (ISE; ABL, topotypes).
Pyrenula musaespora Aptroot & M. Cáceres, sp. nov. (Fig. 5A–B)
Mycobank #811023
Pyrenula with thallus pale ochraceous, with lichexanthone, ascospores filiform, 3–5-septate, 30–37 × 3–4 μm.
Holotype:—BRAZIL. Sergipe: Santa Luzia do Itanhy, Mata do Crasto; 11˚22’S, 37˚25’W; alt. c. 10 m; on bark of
tree; 26 March 2014, M.E.S. Cáceres & A. Aptroot 18759 (ISE; isotype: ABL).
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FIGURE 5. Pyrenula musaespora (isotype ABL); A, habitus showing black ascomata emerging from ochraceous thallus; B, ascospore;
C–D, P. rubrolateralis (isotype ABL); C, habitus showing a red ostiole; D, ascospores; E–F, Thelenella lateralis (isotype ABL); E, habitus
showing white ostioles; F, ascospores. A, C & E: bar = 0.5 mm; B & F: bar = 10 μm; D: bar = 5 μm.
PYRENOCARPOUS LICHENS Phytotaxa 197 (3) © 2015 Magnolia Press 205
Thallus thin, corticate, pale ochraceous, without pseudocyphellae, surrounded by a c. 0.5 mm wide black prothal-
lus line. Ascomata superficial on the bark, conical, 0.4–0.65 mm diam., single, mostly covered by thallus that is reveal-
ing the black ascomata in a rather irregular area around the ostiole. Wall carbonized all around. Ostiole apical, black.
Hamathecium inspersed with hyaline oil droplets. Ascospores 8/ascus, brown, in one bundle (all mostly overlapping),
filiform, 3–5-septate, 30–37 × 3–4 μm, lumina long elongated, separated from the wall by a relatively thick layer of
endospore, ends pointed. Pycnidia not observed. Chemistry: Thallus UV+ yellow; TLC: lichexanthone.
Ecology and distribution:—On smooth bark in undisturbed Atlantic rain forest. Only known from Brazil.
Discussion:—Filiform ascospores are rare in the genus Pyrenula, and there is only one species known with fili-
form ascospores that are also 3–5-septate, viz. P. melanophthalma (Mont.) Trevis. (Trevisan 1853: 17). This species
differs because the hamathecium is not inspersed and the thallus contains no anthraquinone. The new species has the
characteristic ochraceous thallus colour of crustose lichens that contain much lichexanthone in the cortex; it could
therefore already be recognized in the field as a probably undescribed species.
Additional specimen examined:—BRAZIL. Sergipe: Santa Luzia do Itanhy, Mata do Crasto; 11˚22’S, 37˚25’W;
alt. c. 10 m; on bark of tree; 26 March 2014, M.E.S. Cáceres & A. Aptroot 18808 (ISE; ABL, topotypes).
Pyrenula rubrolateralis Aptroot & M. Cáceres, sp. nov. (Fig. 5C–D)
Mycobank #811024
Pyrenula with eccentric red ostioles, ascospores 3-septate, 20–24 × 8–10 μm.
Holotype:—BRAZIL. Sergipe: Santa Luzia do Itanhy, Mata do Crasto; 11˚22’S, 37˚25’W; alt. c. 10 m; on bark of
tree; 26 March 2014, M.E.S. Cáceres & A. Aptroot 18783 (ISE; isotype: ABL).
Thallus rather thin (up to 0.1 mm thick), rather irregular in thickness, corticate, olive green, closely following
the cracks and fissures in the bark, without pseudocyphellae, surrounded by a c. 1 mm wide black prothallus line. As-
comata immersed in raised areas of the bark, almost completely covered by the thallus, pyriform, 0.6–0.9 mm diam.,
single. Wall carbonized all around. Ostiole eccentric, red brown to bright red, flush to distinctly convex. Hamathecium
not inspersed with oil droplets. Ascospores 8/ascus, irregularly biseriate, brown, 3-septate, 20–24 × 8–10 μm, lumina
mostly rounded to somewhat diamond-shaped, separated from the wall by a thick layer of endospore, ends pointed.
Pycnidia not observed. Chemistry: Ostiole K–; thallus UV–; no substances detected with TLC.
Ecology and distribution:—On smooth bark in undisturbed Atlantic rain forest. Only known from Brazil.
Discussion:—This species is characterized by the eccentric red ostioles. It would key out in couplet 31 in key B
in the world key (Aptroot 2012: 20). The closest species is the North American Pyrenula wetmorei R.C. Harris (1990:
69), which differs by the inspersed hamathecium and the Pyrgillus-like ascospores with black pigment bands obscur-
ing the septa.
Thelenella lateralis Aptroot & M. Cáceres, sp. nov. (Fig. 5E–F)
Mycobank #811025
Corticolous Thelenella with eccentric ostiole, ascospores irregularly muriform, 7–9 × 0–2 -septate, 27–32 × 9–10.5 μm.
Holotype:—BRAZIL. Sergipe: Aracaju, Parque da Cidade Governador José Rollemberg Leite; 10˚52’57”S,
37˚03’10”W; alt. c. 75 m; on bark of tree; 15 September 2013, M.E.S. Cáceres & A. Aptroot 18215 (ISE; isotype:
ABL).
Thallus thin, corticate, metallic grey, without pseudocyphellae, without prothallus. Ascomata immersed in the
bark, pyriform, 0.4–0.55 mm diam., single. Wall only carbonized above. Ostiole eccentric, dark grey. Hamathecium
not inspersed with oil droplets, filaments anastomosing. Ascus with ocular chamber. Ascospores 8/ascus, long el-
lipsoid-fusiform, hyaline, irregularly biseriate, irregularly muriform, 7–9 × 0–2 -septate, 27–32 × 9–10.5 μm, ends
rounded or lower end pointed. Pycnidia not observed. Chemistry: No substances detected.
Ecology and distribution:—On smooth bark in a remnant of Atlantic rain forest. Only known from Brazil.
Discussion:—This is the first species in the genus described with eccentric ostioles. It seems closest to Thelenella
paraguayensis Malme (1928: 5), which however has also larger ascospores (42–60 × 13–19 μm).
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Additional specimen examined:—BRAZIL. Sergipe: Aracaju, Parque da Cidade Governador José Rollemberg
Leite; 10˚52’57”S, 37˚03’10”W; alt. c. 75 m; on bark of tree; 15 September 2013, M.E.S. Cáceres & A. Aptroot 18217
(ISE; ABL, topotypes).
Acknowledgements
MESC thanks CNPq—Conselho Nacional de Desenvolvimento Científico e Tecnológico, for a research grant (Processo
311706/2012-6) and for financial support to the collecting trips (INCT-Herbário Virtual Processo 573.883/2008-4
and Sisbiota Processo 563342/2010-2). CAPES—Coordenação de Aperfeiçoamento de Pessoal de Nível Superior is
thanked for Masters scholarship to DSA and for a PhD grant to ELL. The Hugo de Vries-fonds is thanked for travel
support to AA. Leo Spier is thanked for performing thin-layer chromatography.
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http://dx.doi.org/10.2307/3242389
... For literature records, we compiled data from numerous published studies, mostly taxonomic inventories corresponding to the target area (Alves et al., 2014a(Alves et al., , 2014bAndrade, 2015;, 2014c, 2016a, 2016bAptroot, Ertz, et al., 2013, Aptroot, Oliveira, et al., 2013, Aptroot, Sipman, et al., 2013Aptroot, Mendonça, et al., 2014Aptroot, Andrade, et al., 2015, Aptroot, Ertz, et al., 2015, Aptroot, Sobreira, et al., 2015, 2017Cáceres, 2007, 2016Cáceres & Lücking, 2000Cáceres et al., 2008b;Cáceres, Rivas Plata, et al., 2012, Cáceres, Viera, et al., 2012Cáceres, Andrade, et al., 2013, Cáceres, Aptroot, Nelsen, et al., 2013Cáceres, Aptroot, & Ertz, 2014Cáceres, Nascimento, et al., 2014;, Cáceres, Aptroot, Mendonça, et al., 2017, Cáceres, Júnior, et al., 2017Cavalcante, 2012;Dantas, 2016;Dantas et al., 2017;Feuerstein et al., 2014;Frisch & Kalb, 2009;Gueidan et al., 2016;Kalb & Aptroot, 2018;Kalb, 1982aKalb, , 1982bKalb, , 1982cKalb, , 1983aKalb, , 1983bKalb, , 1984Kalb, , 1986Kalb, , 1987Kalb, , 1988Kalb, , 1991Kalb, , 2001Kalb, , 2004Kalb, , 2009Kalb et al., 2009;Lima, 2013Lima, , 2018, Lima, Mendonça, Maia, et al., 2013Lima et al., 2016Lima et al., , 2019Lücking & Cáceres, 1999, 2004Lumbsch et al., 2011;McCarthy, 1995;Mendonça, 2014;Mendonça et al., 2016;Menezes, 2013;Menezes et al., 2011;, Menezes, Xavier-Leite, Costa, et al., 2013, Menezes, Xavier-Leite, Jesus, et al., 2013Oliveira, 2008;Parnmen et al., 2013;Rodrigues, 2012;Santos et al., 2016Santos et al., , 2020Sobreira, 2015;Sobreira et al., 2015Sobreira et al., , 2016Staiger et al., 2006;Sulzbacher et al., 2016;Xavier-Leite, 2013;Xavier-Leite, Menezes, Andrade, et al., 2014Xavier-Leite et al., 2015). For digital records, we mined the online repositories of the Global Biodiversity Information Facility (GBIF; http://www.gbif.org) ...
... For literature records, we compiled data from numerous published studies, mostly taxonomic inventories corresponding to the target area (Alves et al., 2014a(Alves et al., , 2014bAndrade, 2015;, 2014c, 2016a, 2016bAptroot, Ertz, et al., 2013, Aptroot, Oliveira, et al., 2013, Aptroot, Sipman, et al., 2013Aptroot, Mendonça, et al., 2014Aptroot, Andrade, et al., 2015, Aptroot, Ertz, et al., 2015, Aptroot, Sobreira, et al., 2015, 2017Cáceres, 2007, 2016Cáceres & Lücking, 2000Cáceres et al., 2008b;Cáceres, Rivas Plata, et al., 2012, Cáceres, Viera, et al., 2012Cáceres, Andrade, et al., 2013, Cáceres, Aptroot, Nelsen, et al., 2013Cáceres, Aptroot, & Ertz, 2014Cáceres, Nascimento, et al., 2014;, Cáceres, Aptroot, Mendonça, et al., 2017, Cáceres, Júnior, et al., 2017Cavalcante, 2012;Dantas, 2016;Dantas et al., 2017;Feuerstein et al., 2014;Frisch & Kalb, 2009;Gueidan et al., 2016;Kalb & Aptroot, 2018;Kalb, 1982aKalb, , 1982bKalb, , 1982cKalb, , 1983aKalb, , 1983bKalb, , 1984Kalb, , 1986Kalb, , 1987Kalb, , 1988Kalb, , 1991Kalb, , 2001Kalb, , 2004Kalb, , 2009Kalb et al., 2009;Lima, 2013Lima, , 2018, Lima, Mendonça, Maia, et al., 2013Lima et al., 2016Lima et al., , 2019Lücking & Cáceres, 1999, 2004Lumbsch et al., 2011;McCarthy, 1995;Mendonça, 2014;Mendonça et al., 2016;Menezes, 2013;Menezes et al., 2011;, Menezes, Xavier-Leite, Costa, et al., 2013, Menezes, Xavier-Leite, Jesus, et al., 2013Oliveira, 2008;Parnmen et al., 2013;Rodrigues, 2012;Santos et al., 2016Santos et al., , 2020Sobreira, 2015;Sobreira et al., 2015Sobreira et al., , 2016Staiger et al., 2006;Sulzbacher et al., 2016;Xavier-Leite, 2013;Xavier-Leite, Menezes, Andrade, et al., 2014Xavier-Leite et al., 2015). For digital records, we mined the online repositories of the Global Biodiversity Information Facility (GBIF; http://www.gbif.org) ...
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Amazon, Atlantic forest, Brejos de Altitude, Caatinga, Carrasco, Cerradão and Restinga are major vegetation units in North and Northeast Brazil. Little is known about lichen metacommunity structure in these habitats. While species richness and composition generally depend on climatic factors, in azonal vegetation edaphic factors may have a filtering effect on tree bark structure and hence the composition of epiphytic lichen communities. We hypothesized that climatic stress and a tree bark filtering effect would result in reduced richness and phylogenetic clustering in Caatinga, Carrasco, Cerradão and Restinga, whereas high richness and phylogenetic overdispersion were predicted for Amazon and Atlantic Forest. To test this, we analyzed 2,090 lichenized species in the study area, with a supertree to assess phylogenetic metacommunity structure. Amazon and Atlantic forest exhibited high richness and phylogenetic diversity, with phylogenetic overdispersion only in the Amazon. The zonal Caatinga with drought stress and the extrazonal Brejos both exhibited phylogenetic clustering. Among the azonal, edaphic vegetation units, Cerradão exhibited phylogenetic overdispersion, whereas Restinga showed phylogenetic clustering. Nearest taxon phylogenetic distance indicated a close relationship between Amazon and Atlantic forest, Atlantic forest and Brejos and Atlantic forest and Caatinga. Carrasco was mostly closely related to Cerradão, and Restinga was distantly related to any other unit. These findings indicate more complex patterns in the phylogenetic structure of lichen metacommunities, partly reflecting those of plant metacommunities, as a result of concurrent macroecological evolutionary histories. Our data supported floristic evidence that Carrasco is part of the Cerrado complex and not related to Caatinga.
... The lichen genus Pyrenula typically found on smooth and shaded bark mostly in evergreen forest is represented by ca. 226 species in the world (Aptroot 2012;Aptroot et al. 2013Aptroot et al. , 2015Mendonça et al. 2016;Aptroot and Common 2017), of which 92 are known from India (Upreti 1998, Singh and Sinha 2010, Jagadeesh Ram and Sinha 2010. Following the recent world key of the species of Anthracothecium and Pyrenula by Aptroot (2012), at present only 67 species are known from India. ...
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Pyrenula andina, P. atropurpurea, P. bahiana , P. caracasana, P. macrospora, P. massariospora, P. pseudobufonia , P. subducta, P. subgregantula and P. tristissima are described as new records for Indian lichen flora. An updated key to all Pyrenula species so far known from India is also presented.
... In a recent key to the species of the genus Pyrenula, Aptroot (2012) accepted 169 species out of the c. 745 named taxa in the genus. Today the genus has c. 225 accepted species, including the 169 accepted in Aptroot (2012) plus the many additional species that have been described since (Aptroot et al. , 2015Wijeyaratne et al. 2012;Cáceres et al. 2013;Lima et al. 2013;Gueidan et al. 2016;Mendonça et al. 2016). From the genus Pyrgillus, only seven species are currently known (Aptroot 1991;Kashiwadani et al. 2012;Singh & Singh 2012a, b, 2017, and in Sulcopyrenula only four species (Harada 1999;Aptroot 2002Aptroot , 2012. ...
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Eight new species of Pyrenulaceae are described as new to science from Brazil, Guyana and Puerto Rico. Pyrenula sanguineomeandrata Aptroot & Mercado Diaz (with a thallus with red, KOH+ purple pigmentation of lines or a reticulum, simple ascomata with vertical ostioles, a deep red inspersed, KOH+ orange hamathecium, and dark brown 3-septate ascospores 25–29×10–12 μm) and P. sanguineostiolata Aptroot & Mercado Diaz (with a thallus with deeply immersed simple ascomata with vertical ostioles, which are superficial and bright red, and 3-septate ascospores 25–28×9–12 μm) are described from submontane evergreen forests in Puerto Rico. Pyrenula biseptata Aptroot & M. Cáceres (with simple ascomata with vertical ostioles, an inspersed hamathecium and 2-septate ascospores 11–12×4·5–5·0 μm) and P. xanthinspersa Aptroot & M. Cáceres (with an ecorticate thallus containing lichexanthone, simple ascomata with vertical ostioles, not inspersed hamathecium and 3-septate ascospores 14–17×6·0–7·5 μm) are described from rainforest in Amazonian Brazil. Pyrenula subvariabilis Aptroot & Sipman (with fused ascomata with lateral ostioles and submuriform ascospores 17–20(–25)×6–9 μm) and Sulcopyrenula biseriata Aptroot & Sipman (with a thallus containing lichexanthone, simple ascomata with lateral ostioles and lozenge-shaped ascospores with 8 locules, (13–)15–17(–20)×8–10 (width)×6–7 (thickness) μm) are described from savannahs in Guyana. Special attention is paid to the genus Pyrgillus : two new species from the 3-septate core group of this small genus are described from Brazil, viz. P. aurantiacus Aptroot & M. Cáceres (with a corticate thallus containing lichexanthone, mazaedium with orange, KOH+ violet, UV+ red pruina and ascospores of 13–16×6·0–7·5 μm) and P. rufus Aptroot & M. Cáceres (with a corticate thallus containing lichexanthone, mazaedium with dark red, KOH+ orange, UV+ red pruina and ascospores of 15·0–17·5×5·0–6·5 μm). An updated key to the 3-septate species of Pyrgillus is provided.
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The saxicolous and terricolous lichen biota of the Vale do Catimbau in Pernambuco state (Brazil) was studied and with 74 species found to be relatively rich. Most species are new to the state and five are new to Brazil, viz. Andreiomyces ob­ tusatica (Tønsberg) B.P. Hodk. & Lendemer, Caloplaca brittonii (Zahlbr.) Aptroot, Candelariella rosulans (Müll. Arg.) Zahlbr., Clavascidium antillarum (Breuss) Breuss, and Stromatella bermudana (Riddle) Henssen. In addition, some new state records were found of corticolous and lignicolous lichens. A comparison is made with all other places in northeastern Brazil where saxicolous lichens have been studied. For this, the Serra de Itabaiana in Sergipe state was revisited too, and many additional species were recorded there. All places differ markedly in species composition. This seems to be correlated to altitude, biome, and rock type (sandstone versus granite), with the biome mostly influencing the species composition and the altitude the species richness. Some of the species newly reported from Brazil are so far known from the Antilles and there seems to be some resemblance between these lichen biotas.
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In this study we present an analysis of the Pyrenula ochraceoflava group (Pyrenulaceae), focusing on the Neotropics and based on morphological, chemical, and molecular data of the mtSSU, nuLSU and ITS markers. We described three new species from tropical dry forests of Mexico, confirm the monophyly of the P. ochraceoflava group and provide evidence for the inclusion of species currently placed in the genus Mazaediothecium within Pyrenula. Pyrenula aurantiacoretis sp. nov. is characterized by an orange pigment covering the thallus in net-like fashion, muriform ascospores with 4 rows of 1–4 cells each, 12–15.5 x 8–10.5 µm, and 7-chloroemodin and emodin as major compounds. Pyrenula connexa sp. nov. is closely related to Mazaediothecium album, being characterized by mazaedioid pyrenocarps, basal and lateral excipular carbonization, highly variable mature ascospores, 1-septate to submuriform, thallus with abundant white verrucae, and lichexanthone as major compound. Pyrenula moldenkeorum sp. nov. is characterized by an orange thallus, submuriform ascospores that frequently show pigmented septa forming a cross septation pattern, 7.5–11 x 5.5–8.5 µm in size, and 7-chloroemodin and emodin as major compounds. The taxonomy of the most common and widespread species of the group, P. ochraceoflava and P. ochraceoflavens, is briefly discussed, presenting evidence to support the consideration of P. ochraceoflava as a species complex. The two species Mazaedothecium album and M. mohamedii are transferred to Pyrenula as P. aptrootiana nom. nov. [non Pyrenula alba (Schrad.) A.Massal.] and P. mohamedii comb. nov.
Article
The following seven new species of pyrenocarpous lichens are described from Monte Pascoal in Bahia (Brazil): Astrothelium citrisporum Aptroot, Oliveira-Junior & M.Cceres, with thallus ochraceous, UV-negative, ascomata fused in hemispherical, concolorous pseudostromata, hamathecium not inspersed, and ascospores submuriform, 5 12-septate, 3540 1820 m, citriform, both ends pointed; A. eustominspersum Aptroot & Oliveira-Junior, with thallus pale greyish olivaceous, UV-negative, ascomata fused, ostiole UV+ yellow, hamathecium inspersed, and ascospores 3-septate, 2527 77.5 m; A. flavogigasporum Aptroot, with thallus olivaceous, UV-negative, ascomata single, ostioles apical, hamathecium yellowish (K-negative) inspersed, and ascospores 4/ascus, hyaline, densely muriform, 240260 3338 m, long-ellipsoid, without thickened central septum; A. medioincrassatum Aptroot & M.Cceres, with thallus olivaceous, UV-negative, ascomata fused in inconspicuous groups, ostioles lateral, hamathecium not inspersed, and ascospores 911-septate, 98115 2327 m, long-ellipsoid, with thickened central septum; Pseudopyrenula gelatinosa Aptroot, with thallus UV-negative, ascomata solitary, ostioles apical, hamathecium not inspersed, and ascospores 3-septate, 3437 910.5 m, wall 1 m thick, surrounded by a 910.5 m thick gelatinous sheath; Pyrenula salmonea Aptroot, with thallus salmon pink, ascomata solitary, ostioles apical, hamathecium densely hyaline inspersed, and ascospores 3-septate, uniseriate, 2427 1316 m, ellipsoid, lumina oval to somewhat angular, broader than long, without endospore between the outer lumina and the ascospore wall; and P. sanguineoastroidea Aptroot with thallus olivaceous, UV-negative, ascomata fused, deeply immersed in the bark, ostioles lateral, hamathecium not inspersed, and ascospores 3-septate, 2427 1012 m, long-ellipsoid, lumina rhomboid, with thick endospore layer between the outer lumina and the ascospore wall. A further 353 species are reported, of which 12 are first records for Brazil and 192 are first records for the state of Bahia, despite it being one of the states of Brazil that is best investigated lichenologically. A graph is presented with the cumulative number of species collected after a certain time of fieldwork. It does not significantly level off, suggesting that many more species occur in the area. A key to the Pyrenula species known from Brazil is presented.
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Together with Graphidaceae and Trypetheliaceae, Pyrenulaceae forms part of the "big three", the three most speciose, chiefly tropical microlichen families. Microlichens are the most diverse component of tropical lichen communities, with numerous species still to be discovered. Following previous analyses of Graphidaceae and Trypetheliaceae, here we present a global species richness estimate for Pyrenulaceae, using a recently devised method based on a global grid system. We refined this approach by using an iterative adjustment to estimate mean predicted grid range per species from a grid frequency histogram. We also adjusted a previously implemented randomization approach to estimate error margins. Our results showed a global estimate for Pyrenulaceae of (395–)441(–453) species world-wide, 307 of which are currently known, thus an overall predicted increase of over 40%. This includes 416 known and predicted tropical and 25 known, exclusively temperate species, the latter assumed to remain unchanged. While the robustness of the global prediction depends on accurately setting grid sampling scores, individual predicted grid richness varies according to additional factors such as evolutionary history. In addition to undescribed species contribution to predicted richness, we hypothesize that species delimitation studies in presumably widespread taxa will reveal refined species concepts with narrower ranges, thus further increasing estimated global richness. The comparison of predicted richness values for the three families Graphidaceae, Trypetheliaceae and Pyrenulaceae with regard to their evolutionary ages highlights this rather robust method as a promising tool to circumvent sampling and knowledge bias when assessing speciation and diversification patterns.
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As a result of our study, two species of Lepraria (L. atlantica, L. lobata) and two species of Pyrenula (P. duplicans, P. subelliptica) are reported for the first time from China, and Pyrenula pyrenuloides is reported for the first time from Guizhou province.
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Knowledge of the relationships and thus the classification of fungi, has developed rapidly with increasingly widespread use of molecular techniques, over the past 10–15 years, and continues to accelerate. Several genera have been found to be polyphyletic, and their generic concepts have subsequently been emended. New names have thus been introduced for species which are phylogenetically distinct from the type species of particular genera. The ending of the separate naming of morphs of the same species in 2011, has also caused changes in fungal generic names. In order to facilitate access to all important changes, it was desirable to compile these in a single document. The present article provides a list of generic names of Ascomycota (approximately 6500 accepted names published to the end of 2016), including those which are lichen-forming. Notes and summaries of the changes since the last edition of ‘Ainsworth & Bisby’s Dictionary of the Fungi’ in 2008 are provided. The notes include the number of accepted species, classification, type species (with location of the type material), culture availability, life-styles, distribution, and selected publications that have appeared since 2008. This work is intended to provide the foundation for updating the ascomycete component of the “Without prejudice list of generic names of Fungi” published in 2013, which will be developed into a list of protected generic names. This will be subjected to the XIXth International Botanical Congress in Shenzhen in July 2017 agreeing to a modification in the rules relating to protected lists, and scrutiny by procedures determined by the Nomenclature Committee for Fungi (NCF). The previously invalidly published generic names Barriopsis, Collophora (as Collophorina), Cryomyces, Dematiopleospora, Heterospora (as Heterosporicola), Lithophila, Palmomyces (as Palmaria) and Saxomyces are validated, as are two previously invalid family names, Bartaliniaceae and Wiesneriomycetaceae. Four species of Lalaria, which were invalidly published are transferred to Taphrina and validated as new combinations. Catenomycopsis Tibell & Constant. is reduced under Chaenothecopsis Vain., while Dichomera Cooke is reduced under Botryosphaeria Ces. & De Not. (Art. 59).
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An annotated checklist of the lichens of Hong Kong, based on all available literature reports and specimens, including those recently collected by the authors, is presented. In total, 261 species are reported, of which 176 are new records for Hong Kong, 132 of which are new for China, 43 are new for East Asia, and 27 are new for Asia. The lichen vegetation is mainly tropical, as is shown by the distribution patterns of the identified species: 53 species are cosmopolitan, 40 northern temperate, 122 pantropical, 17 paleotropical and 29 endemic to tropical East Asia. With regard to substrata, 129 species are corticolous, 148 saxicolous, 17 foliicolous and 19 terricolous. Four species are newly described: Anisomeridium conorostratum Aptroot, A. hydei Aptroot, Caloplaca pulicarioides Aptroot and Placidiopsis poronioides Aptroot. The flora is rather poor in species; for example, no Caliciales have been found. In the past, the numbers of species of several groups such as the Graphidaceae, Heterodermia and Xanthoparmelia have been overestimated, whereas few pyrenocarps have been reported. The flora of wet granitic outcrops is surprisingly well developed in Hong Kong. Although not a single Peltula species was reported before, six species were identified, including one that was previously only known from Africa. In addition, several other cyanophilic genera are present, such as Euopsis, Psorotichia, Pyrenopsis and, most unexpectedly, Vestergrenopsis, each with one species. A comparison between old and recent records shows that many Lobarion species are now extinct. The drastic decline of species of the Lobarion vegetation indicates that air pollution and other habitat disturbances, mainly deforestation, to which these species are very sensitive, are seriously threatening the lichen biodiversity of Hong Kong.
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Pyrenula sanguinea Aptroot, M. Caceres & Lucking is described from branches of trees in Amazonian rain forest in the state of Rondonia, Brazil. It is characterized by bright red, pseudostromatic ascomata with fused walls, closely resembling those of Trypethelium eluteriae and related species except for the color. The brown ascospores deviate from those of most other Pyrenula species by their reduced endospore formation; they are surrounded by a thick gelatinous sheath with horn-like and curled appendages at the tips. Although morphologically very distinct from all other known species of Pyrenula, molecular data of the mtSSU and nuLSU loci revealed that it is nested within that genus, with a strongly supported sister-group relationship with P. cruenta. Both species share the bright red color of ascomata, but co-chromatography revealed a distinct, complex pattern for P. sanguinea, with six different pigments, only haematommone shared with P. cruenta.
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An identification key is presented for the accepted species of the lichen genera Anthracothecium (comprising 5 species) and Pyrenula (with 169 species, including 7 still undescribed). The key also contains some similar taxa and is complete for Blastodesmia (1 species), Sulcopyrenula (4 species), and Eopyrenula (6 species), but not for others such as Aptrootia, Architrypethelium, and Lithothelium, of which only the corticolous brown-spored taxa are treated. The following new combinations were found to be necessary: Anthracothecium interlatens (Nyl.) Aptroot, Pyrenula breutelii (Müll. Arg.) Aptroot, Pyrenula ceylonensis (Ajay Singh & Upreti) Aptroot, Pyrenula fusispora (Malme) Aptroot, Pyrenula gibberulosa (Vain.) Aptroot, Pyrenula lyoni (Zahlbr.) Aptroot, Pyrenula papillifera (Nyl.) Aptroot, Pyrenula platystoma (Müll. Arg.) Aptroot, Pyrenula schiffneri (Zahlbr.) Aptroot, Pyrenula welwitschii (Upreti & Ajay Singh) Aptroot, and Sulcopyrenula subglobosa (Riddle) Aptroot. Pyrenula sexluminata Aptroot is a new name for Pyrenula quinqueseptata Aptroot, and Pyrenula neosandwicensis Aptroot is a new name for Anthracothecium sandwicense Zahlbr. In addition, all known and many novel synonyms are cited, and the disposition of all other taxa in the two genera Anthracothecium (with 155 names) and Pyrenula (with 745 names) and their generic synonyms. Bogoriella was found to be an older name for Mycomicrothelia.
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The new species Pyrenula reginae and P. rubromamillana are described from NE Brazil. Both have a conspicuous red or orange thallus, an inspersed hamathecium and relatively small ascospores, but they differ clearly in colour and ascoma organization.
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Twenty-three species of Pyrenula from Latin America are treated here. Several species show characters that were not previously reported in the genus and are rare or new to lichenized fungi, viz. yellow, orange or red (KOH+ green) oil inspersion in the hymenium, yellow oil in young ascospores or longitudinal ridges on the ascospore wall. Two taxonomically significant types of over-mature spores are illustrated. The following new species are described: Pyrenula aggregataspistea Aptroot & M. Cáceres, P. aurantioinspersa Aptroot & Sipman, P. cornutispora Aptroot & M. Cáceres, P. flavoinspersa Aptroot & Sipman, P. guyanensis Sipman & Aptroot, P. infraleucotrypa Aptroot & M. Cáceres, P. inframamillana Aptroot & M. Cáceres, P. infrastroidea Aptroot & Sipman, P. maritima Sipman & Aptroot, P. mattickiana Sipman & Aptroot, P. minoides Aptroot & Sipman, P. monospora Aptroot & Sipman, P. paraminarum Aptroot & M. Cáceres, P. perfecta Aptroot & Sipman, P. plicata Sipman & Aptroot, P. rubroinspersa Aptroot & Sipman, P. rubronitidula Aptroot & M. Cáceres, P. rubrostigma Aptroot & M. Cáceres, P. tetraspora Aptroot & Sipman, P. triangularis Aptroot & Sipman, P. viridipyrgilla Aptroot & M. Cáceres. Pyrenula seminuda (Müll. Arg.) Sipman & Aptroot is a new combination.
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A new subgenus (Plagiocarpa subg. Pyrenulopsis R. C. Harris), nine new species and 16 new combinations are established, based on material collected in Louisiana in recent years. Of 31 new reports for Louisiana, eight are new also for the United States. In addition, some new information is provided about 18 other rarely collected species that were found in Louisiana. Clathroporina amygdalina (Müll.Arg.) Fink should be removed from the North American flora and Porina amygdalina Müll.Arg. should be restored.
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Six new species of the genus Pyrenula are described as new to science from various countries in the tropics. Pyrenula borneensis is described from Borneo, P. endocrocea from the Philippines, P. hawaiiensis from Hawaii, P. rinodinospora from Papua New Guinea, P. rubrojavanica from Java, and P. thailandica from Papua New Guinea, India and Thailand.