A preliminary molecular phylogeny of the genus Riccia L. (Ricciaceae) in Australia

2016 ◽  
Vol 29 (3) ◽  
pp. 197 ◽  
Author(s):  
D. Christine Cargill ◽  
Will C. Neal ◽  
Ish Sharma ◽  
Cécile Gueidan

Several Australian Riccia taxa have been sequenced for the first time, with the majority from the monsoon tropics of the Northern Territory, north of 18° latitude. This allowed testing of several infrageneric groupings within the genus as well as morphological species concepts. Molecular data from one nuclear and four plastid markers support the genus as a monophyletic group. However, the monophyly of the two largest subgenera, subgenus Riccia and subgenus Ricciella, are not supported, with the latter being polyphyletic and well nested within subgenus Riccia. Several currently accepted species such as Riccia inflexa and Riccia lamellosa were also found to be polyphyletic. A second tree reconstruction using only trnL–F sequences allowed comparison to several taxa collected outside of Australia. This showed that some species have a truly cosmopolitan distribution, whereas others have not.

Author(s):  
Ayu Savitri Nurinsiyah ◽  
Marco T. Neiber ◽  
Bernhard Hausdorf

A revision of the land snail genus Landouria Godwin-Austin, 1918 (Camaenidae) from Java reveals that this group represents the most diverse land snail radiation on that island. Only six species of Landouria were recognized from Java in the last revision of the genus based on shell characters. Our investigation, which also considers the genitalia as well as DNA sequences, shows that the diversity in Java is much higher. Based on newly collected specimens as well as museum material, twenty-eight species of Landouria from Java are described and figured. To stabilize the nomenclature, neotypes are designated for L. winteriana (Pfeiffer, 1842) and L. rotatoria (Pfeiffer, 1842). Sixteen species are described as new to science, i.e., L. naggsi sp. nov., L. parahyangensis sp. nov., L. nusakambangensis sp. nov., L. petrukensis sp. nov., L. tholiformis sp. nov., L. madurensis sp. nov., L. abdidalem sp. nov., L. sewuensis sp. nov., L. tonywhitteni sp. nov., L. sukoliloensis sp. nov., L. nodifera sp. nov., L. pacitanensis sp. nov., L. zonifera sp. nov., L. pakidulan sp. nov., L. dharmai sp. nov. and L. menorehensis sp. nov. Landouria conoidea (Leschke, 1914) comb. nov., L. intumescens (Martens, 1867) comb. nov., L. moussoniana (Martens, 1867) comb. nov., L. schepmani (Möllendorff, 1897) comb. nov. and L. leucochila (Gude, 1905) comb. nov. are considered valid species of the genus Landouria for the first time. Plectotropis kraepelini Leschke, 1914 syn. nov. is considered a probable synonym of L. winteriana (Pfeiffer, 1842), P. trichotrochium Möllendorff, 1897 syn. nov. is a synonym of L. epiplatia (Möllendorff, 1897) and the preoccupied name Helix squamulosa Martens, 1867 syn. nov. is a synonym of L. madurensis sp. nov. We estimate that there are actually more than fifty species of Landouria in Java because many shell samples could not be classified and because no material is available from several regions of the island. A molecular phylogeny reveals that the species from Java do not form a monophyletic group, but that at least one species from Timor is nested within Javanese clades. This means that the Oriental Landouria crossed Wallace’s line, the supposed border between the Oriental and Australo-Papuan regions, at least twice and supports the conclusion that Wallace’s line does not represent a more severe barrier for terrestrial organisms than other straits through the archipelago. Within the Javanese clades, species from western and eastern Java are mixed, indicating frequent dispersals also within Java.


2020 ◽  
Vol 62 (3-4) ◽  
pp. 293-307
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
M.-H. Jeong ◽  
S.-O. Oh ◽  
A. S. Kondratiuk ◽  
...  

Three genera new for science, i.e. Candelinella S. Y. Kondr. for the Candelariella makarevichiae group, Opeltiella S. Y. Kondr. for the Candelaria fraudans group, as well as Protocandelariella Poelt, D. Liu, J.-S. Hur et S. Y. Kondr. for the Candelariella subdeflexa group are proposed for robust monophyletic branches of the Candelariaceae on the basis of three-gene phylo- geny (i.e. concatenated nrITS, 12S mtSSU and 28S nrLSU sequences). Eight new combinations, i.e. Candelinella makarevichiae (for Candelariella makarevichiae S. Y. Kondr., L. Lokos et J.-S. Hur), Candelinella deppeanae (for Candelariella deppeanae M. Westb.), Opeltiella fraudans (for Candelaria fraudans Poelt et Oberw.), Opeltiella fibrosoides (for Candelaria fibrosoides M. Westb. et Froden), Opeltiella rubrisoli (for Candelariella rubrisoli D. Liu et J.-S. Hur), Opeltiella canadensis (for Candelariella canadensis H. Magn.), Protocandelariella subdeflexa (for Lecanora subdeflexa Nyl.), Protocandelariella blastidiata (for Candelariella blastidiata L. Yakovchenko) are provided.Molecular data provided for Candelinella makarevichiae (including holotype and iso- type), as well as additional specimens of Candelaria asiatica from South Korea for the first time. The latter species (Candelaria asiatica) from China, as well as’Candelaria’ murrayi from Argentina, South America are recorded for the first time. Voucher of Candelariella vitellina from Antarctica is also identified based on molecular phylogeny. It is for the first time shown that ’Candelaria’murrayi is positioned in the outermost position to Candelaria s. str. branch of the phylogenetic tree of the Candelariaceae, and may belong to another genus. Status of the ’Candelariella’medians group, the’Candelariella’ placodizans group, as well as single species ’Candelariella’reflexa and’Candelaria’ pacifica, forming separate branches outside the Candelariella s. str. and Candelaria s. str. clades, will be clarified when additional molecular data will be accumulated. Candelariella subsquamulosa D. Liu et Hur, recently described from South Korea (Liu et al. 2019), proved to be a new synonym of Candelinella makarevichiae.


MycoKeys ◽  
2020 ◽  
Vol 63 ◽  
pp. 163-172
Author(s):  
Xiao-Lan He ◽  
Egon Horak ◽  
Di Wang ◽  
Tai-Hui Li ◽  
Wei-Hong Peng ◽  
...  

Entoloma subgenus Claudopus is widely distributed, yet the taxonomy and systematics of its species are still poorly documented. In the present study, more than forty collections of Claudopus were gathered in China and subsequently analysed, based on morphological and molecular data. The results revealed first a high level of species diversity of Claudopus in China and second, there is a wide ecological range regarding the substrates and the habitats ranging from temperate, tropical to subalpine locations. Based on morphological and molecular evidence, five novel species from China are proposed, viz. E. conchatum, E. flabellatum, E. gregarium, E. pleurotoides and E. reductum. Molecular phylogeny of Entoloma s.l. was also reconstructed, based on 187 representatives of Entoloma s.l. by employing the combined ITS, LSU, mtSSU and RPB2 sequences. Ten monophyletic clades (Claudopus, Leptonia, Nolanea, Cuboid-spored Inocephalus, “Alboleptonia”, Cyanula, Pouzarella, Rhodopolia, Prunuloides and Rusticoides) were recovered, while 13 taxa could not be placed in any defined clades. The results confirmed that Claudopus in a traditional morphological sense is not monophyletic and the Rusticoides-group, previously considered within Claudopus, formed a separate clade; but section Claudopus and relatives of E. undatum belong to a distinctive monophyletic group. Despite some monophyletic groups in Entoloma s.l. being distinctive in both morphology and molecular phylogeny, they were still treated as subgenera of Entoloma s.l. temporarily, because accepting them as genera will make Entoloma s.l. paraphyletic.


MycoKeys ◽  
2019 ◽  
Vol 61 ◽  
pp. 1-26
Author(s):  
Xiao-Lan He ◽  
Egon Horak ◽  
Di Wang ◽  
Tai-Hui Li ◽  
Wei-Hong Peng ◽  
...  

Entoloma subgenus Claudopus is widely distributed, yet the taxonomy and systematics of its species are still poorly documented. In the present study, more than forty collections of Claudopus were gathered in China and subsequently analysed, based on morphological and molecular data. The results revealed first a high level of species diversity of Claudopus in China and second, there is a wide ecological range regarding the substrates and the habitats ranging from temperate, tropical to subalpine locations. Based on morphological and molecular evidence, five novel species from China are proposed, viz. E. conchatum, E. flabellatum, E. gregarium, E. pleurotoides and E. reductum. Molecular phylogeny of Entoloma s.l. was also reconstructed, based on 187 representatives of Entoloma s.l. by employing the combined ITS, LSU, mtSSU and RPB2 sequences. Ten monophyletic clades (Claudopus, Leptonia, Nolanea, Cuboid-spored Inocephalus, “Alboleptonia”, Cyanula, Pouzarella, Rhodopolia, Prunuloides and Rusticoides) were recovered, while 13 taxa could not be placed in any defined clades. The results confirmed that Claudopus in a traditional morphological sense is not monophyletic and the Rusticoides-group, previously considered within Claudopus, formed a separate clade; but section Claudopus and relatives of E. undatum belong to a distinctive monophyletic group. Despite some monophyletic groups in Entoloma s.l. being distinctive in both morphology and molecular phylogeny, they were still treated as subgenera of Entoloma s.l. temporarily, because accepting them as genera will make Entoloma s.l. paraphyletic.


2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Sahar Khodami ◽  
J. Vaun McArthur ◽  
Leocadio Blanco-Bercial ◽  
Pedro Martinez Arbizu

Abstract For the first time, the phylogenetic relationships between representatives of all 10 copepod orders have been investigated using 28S and 18S rRNA, Histone H3 protein and COI mtDNA. The monophyly of Copepoda (including Platycopioida Fosshagen, 1985) is demonstrated for the first time using molecular data. Maxillopoda is rejected, as it is a polyphyletic group. The monophyly of the major subgroups of Copepoda, including Progymnoplea Lang, 1948 (=Platycopioida); Neocopepoda Huys and Boxshall, 1991; Gymnoplea Giesbrecht, 1892 (=Calanoida Sars, 1903); and Podoplea Giesbrecht, 1892, are supported in this study. Seven copepod orders are monophyletic, including Platycopioida, Calanoida, Misophrioida Gurney, 1933; Monstrilloida Sars, 1901; Siphonostomatoida Burmeister, 1834; Gelyelloida Huys, 1988; and Mormonilloida Boxshall, 1979. Misophrioida (=Propodoplea Lang, 1948) is the most basal Podoplean order. The order Cyclopoida Burmeister, 1835, is paraphyletic and now encompasses Poecilostomatoida Thorell, 1859, as a sister to the family Schminkepinellidae Martinez Arbizu, 2006. Within Harpacticoida Sars, 1903, both sections, Polyarthra Lang, 1948, and Oligoarthra Lang, 1948, are monophyletic, but not sister groups. The order Canuelloida is proposed while maintaining the order Harpacticoida s. str. (Oligoarthra). Cyclopoida, Harpacticoida and Cyclopinidae are redefined, while Canuelloida ordo. nov., Smirnovipinidae fam. nov. and Cyclopicinidae fam. nov are proposed as new taxa.


Phytotaxa ◽  
2019 ◽  
Vol 416 (4) ◽  
pp. 243-256 ◽  
Author(s):  
DHANDEVI PEM ◽  
RAJESH JEEWON ◽  
TIMUR BULGAKOV ◽  
YUSUFJON GAFFOROV ◽  
SINANG HONGSANAN ◽  
...  

Thyrostroma ephedricola, isolated from Ephedra equisetina from Uzbekistan is introduced as a new species and a new combination, Thyrostroma jaczewskii (B. Sutton) is proposed. Both species are characterised by sporodochial, punctiform conidiomata, and brown cylindrical to subcylindrical, 1–3-septate conidiophores, cylindrical, clavate, or ellipsoid to pyriform brown conidia. Phylogenetic reconstruction based on analyses of ribosomal DNA (ITS, LSU and SSU regions) of Thyrostroma species, strongly supports the recognized taxa as a monophyletic group. The introduction of the new species is supported by both morphological and molecular data.


2021 ◽  
Vol 63 (3-4) ◽  
pp. 351-390
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
I. Kärnefelt ◽  
A. Thell ◽  
M.-H. Jeong ◽  
...  

Seven genera new to science, i.e.: Helmutiopsis, Huriopsis, Johnsheardia, Klauskalbia, Kudratovia, Kurokawia and Poeltonia of the Physciaceae are proposed for the ‘Rinodina’ atrocinerea, the ‘Rinodina’ xanthophaea, the ‘Rinodina’ cinnamomea, the ‘Heterodermia’ obscurata, the ‘Rinodina’ straussii, the ‘Anaptychia’ isidiata and the ‘Physconia’ grisea groups consequently that all form strongly supported monophyletic branches in a phylogeny analysis based on a combined matrix of nrITS and mtSSU sequences. Phylogenetic positions of species belonging to the genera Kashiwadia s. l., Leucodermia, Mischoblastia,Oxnerella, Phaeorrhiza s. l., Polyblastidium and Rinodinella s. l. are discussed. Oxnerella afghanica which for the first time recorded as parasitic lichen species from both epiphytic and saxicolous crustose lichens is designated as type species for the genus Oxnerella. Sequences of the recently described Physcia orientostellaris as well as Huriopsis xanthophaea and additional sequences of Kashiwadia aff. orientalis and Mischoblastia aff. oxydata are submitted to the GenBank. The positions of Polyblastidium casaterrinum from Costa Rica, ‘Rinodina’ efflorescens from Białowieża, Poland, and ‘Mischoblastia’ confragosula from Cambodia in the Physciaceae are confirmed in a phylogeny analysis based on the nrITS sequences. The presence of ‘extraneous mycobiont DNA’ in lichen associations is exemplified with earlier incorrect identifications of Heterodermia, Kashiwadia, Kurokawia,Oxnerella and Poeltonia specimens. Fifty-six new combinations are presented: Helmutiopsis alba (for Rinodina alba Metzler ex Arn.), Helmutiopsis aspersa (for Lecanora aspersa Borrer), Helmutiopsis atrocinerea (for Parmelia atrocinerea Fr.), Huriopsis chrysidiata (for Rinodina chrysidiata Sheard), Huriopsis chrysomelaena (for Rinodina chrysomelaena Tuck.), Huriopsis lepida (for Lecanora lepida Nyl.), Huriopsis luteonigra (for Rinodina luteonigra Zahlbr.), Huriopsis plana (for Rinodina plana H. Magn.), Huriopsis thiomela (for Lecanora thiomela Nyl.), Huriopsis xanthomelana (for Rinodina xanthomelana Müll. Arg.), Huriopsis xanthophaea (for Lecanora xanthophaea Nyl.), Johnsheardia cinnamomea (for Rinodina mniaroea var. cinnamomea Th. Fr.), Johnsheardia herteliana (for Rinodina herteliana Kaschik), Johnsheardia jamesii (for Rinodina jamesii H. Mayrhofer), Johnsheardia reagens (for Rinodina reagens Matzer et H. Mayrhofer), Johnsheardia zwackhiana (for Lecanora zwackhiana Kremp.), Kashiwadia austrostellaris (for Physcia austrostellaris Elix), Kashiwadia jackii (for Physcia jackii Moberg), Kashiwadia littoralis for Physcia littoralis Elix), Kashiwadia nubila (for Physcia nubila Moberg), and Kashiwadia tropica (for Physcia tropica Elix), Klauskalbia crocea (for Heterodermia crocea R. C. Harris), Klauskalbia flabellata (for Parmelia flabellata Fée), Klauskalbia obscurata (for Physcia speciosa (Wulfen) Nyl. *obscurata Nyl.), Klauskalbia paradoxa (for Heterodermia paradoxa Schumm et Schäfer-Verwimp), Kudratovia bohlinii (for Rinodina bohlinii H. Magn.), Kudratovia candidogrisea (for Rinodina candidogrisea Hafellner, Muggia et Obermayer), Kudratovia luridata (for Buellia luridata Körb.), Kudratovia metaboliza (for Rinodina metaboliza Vain.), Kudratovia pycnocarpa (for Rinodina pycnocarpa H. Magn.), Kudratovia roscida (for Lecanora roscida Sommerf.), Kudratovia straussii (for Rinodina straussii J. Steiner), Kudratovia terrestris (for Rinodina terrestris Tomin), Kurokawia bryorum (for Anaptychia bryorum Poelt), Kurokawia isidiata (for Anaptychia isidiata Tomin), Kurokawia mereschkowskii (for Physcia mereschkowskii Tomin), Kurokawia palmulata (for Psoroma palmulatum Michx.), Kurokawia runcinata (for Lichen runcinatus With.), Kurokawia stippea (for Parmelia aquila var. stippea Ach.), Lecania safavidiorum (for Oxnerella safavidiorum S. Y. Kondr., Zarei-Darki, Lőkös et Hur), Leucodermia erinacea (for Lichen erinaceus Ach.), Mischoblastia confragosula (for Lecanora confragosula Nyl.), Mischoblastia destituta (for Lecidea destituta Nyl.), Mischoblastia moziana (for Lecanora moziana Nyl.), Mischoblastia moziana subsp. parasitica (comb. et stat. nova for Rinodina moziana var. parasitica Kaschik et H. Mayrhofer), Mischoblastia ramboldii (for Rinodina ramboldii Kaschik), Mischoblastia vezdae (for Rinodina vezdae H. Mayrhofer), Oxnerella afghanica (for Rinodina afghanica M. Steiner et Poelt), Oxnerella castanomelodes (for Rinodina castanomelodes H. Mayrhofer et Poelt), Physciella nigricans (for Lecanora nigricans Flörke), Poeltonia elegantula (for Physconia elegantula Essl.), Poeltonia grisea (for Lichen griseus Lam.), Poeltonia isidiomuscigena (for Physconia isidiomuscigena Essl.), Poeltonia perisidiosa (for Physcia perisidiosa Erichsen), Poeltonia venusta (for Parmelia venusta Ach.), and Polyblastidium albicans (for Parmelia albicans Pers.) are proposed.


Phytotaxa ◽  
2015 ◽  
Vol 239 (1) ◽  
pp. 17
Author(s):  
Larissa Bernardino Moro ◽  
Gregorio Delgado ◽  
Iracema Helena SCHOENLEIN-CRUSIUS

Clathrosporium retortum sp. nov., collected on submerged mixed leaf litter samples at Ilha do Cardoso State Park, São Paulo state, Brazil, is described based on morphological and molecular data. The fungus is characterized by forming whitish, dense, subglobose to irregular propagules, hyaline to subhyaline when young, subhyaline to dark brown at maturity, that are formed by densely interwoven conidial filaments with each conidial cell repeatedly branching bilaterally or occasionally unilaterally. Phylogenetic analyses using partial LSU nrDNA sequence data suggest that C. retortum belongs in the Sordariomycetes (Ascomycota) where it forms a well-supported clade with Clohesia corticola in the Sordariomycetidae, but its ordinal or familial placement remains unresolved. Its phylogenetic placement confirms the polyphyletic nature of aeroaquatic fungi like Clathrosporium, as it was distantly related to one available sequence in GenBank named as C. intricatum, the type species, which is phylogenetically related to the Helotiales (Leotiomycetes). However, due to lack of authenticity of the identity of this sequence with the type specimen of C. intricatum, a broad concept of Clathrosporium is tentatively adopted here to accommodate the present fungus instead of introducing a new genus. Beverwykella clathrata, Helicoön septatissimum and Peyronelina glomerulata are recorded for the first time from Brazil. Cancellidium applanatum and Candelabrum brocchiatum are new records for the state of São Paulo.


IAWA Journal ◽  
2012 ◽  
Vol 33 (4) ◽  
pp. 337-353 ◽  
Author(s):  
Marc S. Appelhans ◽  
Bertie Joan van Heuven ◽  
Frederic Lens ◽  
Pieter Baas

Subfamily Spathelioideae of Rutaceae constitutes a well-supported early branching clade of eight small woody genera that were formerly assigned to five different Sapindalean/Rutalean families. This study brings together detailed wood anatomical information on all eight genera (for four the wood anatomy is described for the first time in detail). Wood anatomy strongly supports the inclusion of all Spathelioid genera in Rutaceae and underpins the molecular phylogeny with a set of interesting apomorphies at different nodes of the cladogram. The wood anatomy of Cneorum tricoccon with its semi-ring porosity, dendritic vessel pattern, vascular tracheids and helical vessel wall thickenings stands out in Spathelioideae. This wood anatomical syndrome is hypothesized to be due to adaptive evolution for hydraulic safety and efficiency of this species in a typical Mediterranean climate, where similar syndromes have evolved in many unrelated clades of woody dicots. In at least six unrelated genera of Rutaceae outside Spathelioideae from Mediterranean or cool temperate and montane climates, the syndrome has also evolved in presumably parallel, adaptive evolution.


2008 ◽  
Vol 98 (5) ◽  
pp. 499-507 ◽  
Author(s):  
H.C. Zhang ◽  
G.X. Qiao

AbstractThree traditional tribes of Fordini, Pemphigini and Eriosomatini comprise Pemphiginae, and there are two subtribes in Fordini and Pemphigini, respectively. Most of the species in this subfamily live heteroecious holocyclic lives with distinct primary host specificity. The three tribes of Pemphigini (except Prociphilina), Eriosomatini and Fordini use three families of plants, Salicaceae (Populus), Ulmaceae (Ulums) and Anacardiaceae (Pistacia and Rhus), as primary hosts, respectively, and form galls on them. Therefore, the Pemphigids are well known as gall makers, and their galls can be divided into true galls and pseudo-galls in type. We performed the first molecular phylogenetic study of Pemphiginae based on molecular data (EF-1α sequences). Results show that Pemphiginae is probably not a monophylum, but the monophyly of Fordini is supported robustly. The monophyly of Pemphigini is not supported, and two subtribes in it, Pemphigina and Prociphilina, are suggested to be raised to tribal level, equal with Fordini and Eriosomatini. The molecular phylogenetic analysis does not show definite relationships among the four tribes of Pemphiginae, as in the previous phylogenetic study based on morphology. It seems that the four tribes radiated at nearly the same time and then evolved independently. Based on this, we can speculate that galls originated independently four times in the four tribes, and there is no evidence to support that true galls are preceded by pseudo-galls, as in the case of thrips and willow sawflies.


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