Trillium hibbersonii (Melanthiaceae), a phylogenetically distinct species from western North America

Phytotaxa ◽  
2020 ◽  
Vol 436 (2) ◽  
pp. 193-195
Author(s):  
DARLENE M. O’NEILL ◽  
SUSAN B. FARMER ◽  
AARON FLODEN ◽  
JAYNE LAMPLEY ◽  
EDWARD E. SCHILLING

Trillium Linnaeus (1753: 339) species have a reputation for being difficult to distinguish from one another, both on morphological (e.g. Freeman 1985, Schilling et al. 2019) and initial studies with standard plastid markers (Osaloo et al. 1999). Thus, the species that is sister to the rest of the Parideae, Pseudotrillium rivale (Watson 1885: 378) Farmer (2002: 687), was only recognized to be distinctive after DNA sequence data became available (Farmer & Schilling 2002). In the somewhat similar case discussed here, an entity that was considered to be only a form or variety of one species, T. ovatum Pursh (1803: 216), has turned out to be so genetically distinct that it is not even placed in the same clade as T. ovatum (Farmer 2006, Lampley et al. unpubl.).

2011 ◽  
Vol 43 (6) ◽  
pp. 561-567 ◽  
Author(s):  
K. PAPONG ◽  
G. KANTVILAS ◽  
H. T. LUMBSCH

AbstractThe phylogenetic placement of the genus Maronina was studied, based chiefly on phenotypic characters such as thallus colour and anatomy, secondary chemistry, the anatomy of the excipulum and the ascus-type. DNA sequence data of mitochondrial and nuclear ribosomal loci from some of the species support the hypothesis that Maronina is nested within Protoparmelia. Hence, Maronina is reduced to synonymy with Protoparmelia. Comparison of genetic distances suggests that the two varieties within M. orientalis should be regarded as distinct species. Consequently, the new combinations Protoparmelia australiensis (Hafellner & R. W. Rogers) Kantvilas et al., P. corallifera (Kantvilas & Papong) Kantvilas et al., P. hesperia (Kantvilas & Elix) Kantvilas et al., P. multifera (Nyl.) Kantvilas et al., and P. orientalis (Kantvilas & Papong) Kantvilas et al. are proposed.


Phytotaxa ◽  
2015 ◽  
Vol 204 (4) ◽  
pp. 253 ◽  
Author(s):  
YONG-YU SU ◽  
YI-LANG HUANG ◽  
LI-JUN CHEN ◽  
PEI-WEN ZHANG ◽  
Zhong-Jian Liu ◽  
...  

A new orchid species, Liparis wenshanensis, discovered in Yunnan, China is described and illustrated in this study based on morphological and molecular analyses. A detailed comparison between the newly discovered orchid and other members of the genus, Liparis, was conducted. The new plant is characterized by the combination of the following features: a long rachis with 45 to 55 flowers; white sepals, petals and column; a greenish lip with a purplish center; strongly recurved and revolute dorsal sepals and petals; strongly recurved, oblong lateral sepals; a cordate lip that is strongly deflexed below the middle, with a two-lobed apex and a two-lobed callus at the base; an arcuate column with a lamella extending along the center almost to the stigma, and with a pair of broad wings toward the apex. These features distinguish the new orchid from all other known species of Liparis. We proceeded to a phylogenetic analysis to ascertain the systematic position of this enigmatic species. Molecular analyses based on nuclear ribosomal ITS and plastid matK DNA sequence data supports the recognition of L. wenshanensis as a distinct species.


2016 ◽  
Vol 54 (11) ◽  
pp. 2813-2819 ◽  
Author(s):  
Kerry O'Donnell ◽  
Deanna A. Sutton ◽  
Nathan Wiederhold ◽  
Vincent A. R. G. Robert ◽  
Pedro W. Crous ◽  
...  

Multilocus DNA sequence data were used to assess the genetic diversity and evolutionary relationships of 67Fusariumstrains from veterinary sources, most of which were from the United States. Molecular phylogenetic analyses revealed that the strains comprised 23 phylogenetically distinct species, all but two of which were previously known to infect humans, distributed among eight species complexes. The majority of the veterinary isolates (47/67 = 70.1%) were nested within theFusarium solanispecies complex (FSSC), and these included 8 phylospecies and 33 unique 3-locus sequence types (STs). Three of the FSSC species (Fusarium falciforme,Fusarium keratoplasticum, andFusariumsp. FSSC 12) accounted for four-fifths of the veterinary strains (38/47) and STs (27/33) within this clade. Most of theF. falciformestrains (12/15) were recovered from equine keratitis infections; however, strains ofF. keratoplasticumandFusariumsp. FSSC 12 were mostly (25/27) isolated from marine vertebrates and invertebrates. Our sampling suggests that theFusarium incarnatum-equisetispecies complex (FIESC), with eight mycoses-associated species, may represent the second most important clade of veterinary relevance withinFusarium. Six of the multilocus STs within the FSSC (3+4-eee, 1-b, 12-a, 12-b, 12-f, and 12-h) and one each within the FIESC (1-a) and theFusarium oxysporumspecies complex (ST-33) were widespread geographically, including three STs with transoceanic disjunctions. In conclusion, fusaria associated with veterinary mycoses are phylogenetically diverse and typically can only be identified to the species level using DNA sequence data from portions of one or more informative genes.


Plant Disease ◽  
2010 ◽  
Vol 94 (2) ◽  
pp. 279-279 ◽  
Author(s):  
A. M. Minnis ◽  
A. Y. Rossman ◽  
D. L. Clement ◽  
M. K. Malinoski ◽  
K. K. Rane

Callery pear, often referred to as Bradford pear, is a species native to China that is planted throughout North America as an ornamental tree for its white flowers in spring, bright colored foliage in autumn, and resistance to disease. In some regions it is becoming an invasive species that is replacing native trees. In May 2009, leaves of Pyrus calleryana ‘Cleveland Select’ showing distortion and signs of powdery mildew were collected in Columbia (Howard County), Maryland. A survey of the surrounding area found numerous similarly diseased trees of this cultivar. Microscopic observation of the leaves revealed a fungus with an Oidium anamorph having nipple-shaped appressoria; conidiophores erect, foot cells cylindric, straight, of terminal origin, 41 to 55 × 9.5 to 12.5 μm, with the following cells present in variable numbers; conidia catenulate, broadly ellipsoid to rarely slightly ovoid, 22 to 27 × 11 to 17 μm, with fibrosin bodies. Chasmothecia were absent. On the basis of morphology and host, the fungus was identified as Podosphaera leucotricha (Ellis & Everh.) E.S. Salmon (Leotiomycetes, Erysiphales) (1). The specimen on P. calleryana was deposited in the U.S. National Fungus Collections as BPI 879141. Additional confirmation resulted from a comparison of internal transcribed spacer (ITS) region DNA sequence data (GenBank Accession No. GU122230) obtained with the custom designed primer, Podoprimer Forward (5′-3′ ACTCGTTCTGCGCGGCTGAC), and the ITS4 primer. The sequence of the fungus on Callery pear was identical to available GenBank sequences of P. leucotricha. P. leucotricha is the etiological agent of a powdery mildew disease that occurs on rosaceous plants, primarily Malus and Pyrus. This fungus occurs nearly worldwide (1), and the pathology of the disease on Callery pear is similar to that of known hosts (1,4). To our knowledge, this is the first report of P. leucotricha on Pyrus calleryana in North America. P. leucotricha has been reported previously only once on Callery pear, Pyrus calleryana ‘Chanticleer’, in Hungary (4). Additionally, the powdery mildew fungus was heavily parasitized by Ampelomyces quisqualis Ces. sensu lato, a cosmopolitan coelomycetous mycoparasite of the Erysiphales that is well known on this species (2,3). ITS region DNA sequence data from the Ampelomyces (GenBank Accession No. GU122231) obtained with the ITS1 and ITS4 primers was identical to that of other isolates parasitic on P. leucotricha (2). References: (1) U. Braun. The Powdery Mildews (Erysiphales) of Europe. Gustav Fischer Verlag, Jena, Germany, 1995. (2) C. Liang et al. Fungal Divers. 24:225, 2007. (3) B. C. Sutton. The Coelomycetes. Fungi Imperfecti with Pycnidia, Acervuli and Stromata. Commonwealth Mycological Institute, Kew, England, 1980. (4) L. Vajna and L. Kiss. Plant Dis. 92:176, 2008.


2020 ◽  
Vol 86 (2) ◽  
pp. 120-138
Author(s):  
Yuri I Kantor ◽  
Nicolas Puillandre ◽  
Philippe Bouchet

Abstract According to a recent taxonomic revision by Kantor et al. (2001), the neogastropod genus Exilia Conrad, 1860, comprises ten mostly rare species that live at depths between 200 and 2000 m. Adult Exilia measure between 30 and 90 mm in shell length, and the genus is mostly represented in museum collections by empty shells. The abundance of this genus is low in the wild, but recent expeditions organized by the Muséum national d’Histoire naturelle have yielded several dozen specimens. These new collections include samples preserved for molecular studies. Here, we present the results of the first molecular systematic study of Exilia. Our aim was to investigate the species limits proposed by Kantor et al. (2001) on the basis of shell and anatomical characters. Analysis of DNA sequence data for the cytochrome c oxidase I gene suggests that Exilia hilgendorfi, previously considered to be a single, polymorphic and broadly distributed species, is a complex of at least six species (four of which we sequenced). Two of these species, Exilia cognata n. sp. and E. fedosovi n. sp., are described as new to science. Exilia gracilior, E. claydoni and E. prellei are resurrected from the synonymy of Exilia hilgendorfi; of these three, only the last was sequenced. Exilia vagrans is a well-defined taxon, but our molecular systematic data shows that it consists of two distinct species, which occur sympatrically off Taiwan and are strikingly similar in shell and radular morphology; due to the absence of DNA sequence data from the type locality of E. vagrans (Vanuatu), it is unclear to which of these two species the name would apply. Exilia karukera n. sp., which is conchologically very similar to E. vagrans, was discovered off Guadeloupe, represents the first record of the genus from the Atlantic. For E. elegans, which was previously known only from a single shell, we provide new data including new distributional records (South Africa and the Mozambique Channel), details of the radula and DNA sequence data.


1997 ◽  
Vol 29 (5) ◽  
pp. 441-454 ◽  
Author(s):  
Urs Groner ◽  
Scott LaGreca

AbstractRamalina panizzei De Not. is reported from Switzerland and north of the Alps for the first time. Recent collections and thalli found amongst specimens of R. fastigiata (Pers.) Ach. are described; the species is obviously not restricted to the Mediterranean. The confusion in several herbaria around this and related corticolous species, particularly R. subgeniculata Nyl. and R. fastigiata, can be traced back to imprecise original and subsequent diagnoses, all of which lack a clear species delimitation. Similarities and differences of these species are discussed. In addition, sequences from the rDNA ITS regions were determined for two individuals of R. panizzei and two of R. fastigiata, including one of each from a site where both species grow intermixed. Kimura 2-parameter genetic-distance estimates indicate that R. panizzei and R. fastigiata are as different from each other as either is from the reference species R. siliquosa (Hudson) A. L. Sm. s.l. A broad-based taxonomic revision of involved species is not possible due to the limited number of analyses, but the results demonstrate the potential for using DNA sequence data to investigate species-level questions in lichens. Based on morphology, chemistry, and DNA sequence data, R. panizzei is retained as a distinct species.


2017 ◽  
Vol 49 (2) ◽  
pp. 117-126 ◽  
Author(s):  
Lidia S. YAKOVCHENKO ◽  
Jan VONDRÁK ◽  
Yoshihito OHMURA ◽  
Evgeny S. KORCHIKOV ◽  
Olga S. VONDRÁKOVA ◽  
...  

AbstractCandelariella blastidiata Yakovchenko sp. nov. is described. This corticolous species is characterized by biatorine yellow apothecia, a grey squamulose thallus with marginal and lower side blastidia, 8-spored asci, and a northern circumpolar distribution. Candelariella subdeflexa has previously been confused with C. blastidiata, but our analyses of phenotypic and DNA sequence data revealed C. blastidiata should be distinguished from C. subdeflexa. A worldwide key for Candelariella species with grey thalli is provided.


Phytotaxa ◽  
2017 ◽  
Vol 323 (2) ◽  
pp. 182
Author(s):  
SHI-MING FAN ◽  
JIANG-FENG LIU ◽  
JUN-WEN ZHAI ◽  
CHENG-ZI YANG ◽  
ZE-HAO HUANG

A new orchid species, Liparis meihuashanensis, from Fujian, China is described and illustrated based on morphological and molecular analyses. Detailed morphological comparisons indicate that L. meihuashanensis is similar to L. auriculata and L. pauliana, but it can be distinguished from them by the shorter inflorescence, triangular floral bract, and a lip with a truncate-emarginate and mucronate apex and 2 small subconical calli on contracted base. Molecular analyses based on nuclear ITS and plastid matK DNA sequence data support the L. meihuashanensis as a distinct species.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Heleen Plaisier ◽  
Thomas R. Meagher ◽  
Daniel Barker

Abstract Objective Visualisation methods, primarily color-coded representation of sequence data, have been a predominant means of representation of DNA data. Algorithmic conversion of DNA sequence data to sound—sonification—represents an alternative means of representation that uses a different range of human sensory perception. We propose that sonification has value for public engagement with DNA sequence information because it has potential to be entertaining as well as informative. We conduct preliminary work to explore the potential of DNA sequence sonification in public engagement with bioinformatics. We apply a simple sonification technique for DNA, in which each DNA base is represented by a specific note. Additionally, a beat may be added to indicate codon boundaries or for musical effect. We report a brief analysis from public engagement events we conducted that featured this method of sonification. Results We report on use of DNA sequence sonification at two public events. Sonification has potential in public engagement with bioinformatics, both as a means of data representation and as a means to attract audience to a drop-in stand. We also discuss further directions for research on integration of sonification into bioinformatics public engagement and education.


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