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MycoKeys ◽  
2021 ◽  
Vol 85 ◽  
pp. 31-56
Author(s):  
Ning Jiang ◽  
Hermann Voglmayr ◽  
Chun-Gen Piao ◽  
Yong Li

Diaporthe (Diaporthaceae, Diaporthales) is a common fungal genus inhabiting plant tissues as endophytes, pathogens and saprobes. Some species are reported from tree branches associated with canker diseases. In the present study, Diaporthe samples were collected from Alnus glutinosa, Fraxinus excelsior and Quercus robur in Utrecht, the Netherlands. They were identified to species based on a polyphasic approach including morphology, pure culture characters, and phylogenetic analyses of a combined matrix of partial ITS, cal, his3, tef1 and tub2 gene regions. As a result, four species (viz. Diaporthe pseudoalnea sp. nov. from Alnus glutinosa, Diaporthe silvicola sp. nov. from Fraxinus excelsior, D. foeniculacea and D. rudis from Quercus robur) were revealed from tree branches in the Netherlands. Diaporthe pseudoalnea differs from D. eres (syn. D. alnea) by its longer conidiophores. Diaporthe silvicola is distinguished from D. fraxinicola and D. fraxini-angustifoliae by larger alpha conidia.


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 ◽  
2021 ◽  
Vol 523 (2) ◽  
pp. 141-154
Author(s):  
ATENA SAFI ◽  
MEHDI MEHRABI-KOUSHKI ◽  
REZA FAROKHINEJAD

Rapeseed (Brassica napus subsp. napus) is one of the autumn crops in Iran. A new fungal species isolated from internal tissues associating a typical leaf spot of Rapeseed in Dezful (southwestern Iran) was described and illustrated. The sampling and isolation were performed in the late fall of 2019 (during December), which led to obtain the colonies with the similar morphology. Molecular phylogenetic analyses based on a combined matrix of the internal transcribed spacer regions 1 and 2 including the intervening 5.8S nuclear ribosomal DNA (ITS), and partial regions of the β-tubulin (tub2) and RNA polymerase II second largest subunit (rpb2) indicated that two isolated strains represent a new Plenodomus species in family Leptosphaeriaceae (Pleosporales). These novel strains formed a sister lineage with P. biglobosus in our phylogenetic analyses, while, observed morphology is distinguished the taxa from P. biglobosus by its pycnidia in having hyphal outgrowths and lacking cylindrical neck. Accordingly, P. dezfulensis sp. nov. was introduced and its pathogenicity was investigated. Pathogenicity test with both P. dezfulensis strains on three-week seedlings of Rapeseed reproduced leaf spot symptoms. These results approve P. dezfulensis as the causal agent of leaf spot observed on Rapeseed in Dezful.


2021 ◽  
Vol 40 (1) ◽  
pp. 255-271
Author(s):  
Maria T. Gassó ◽  
Iván Gil ◽  
Isabel Giménez ◽  
Máximo Santana ◽  
Elaine Segura

The study of the diagonal entries of the combined matrix of a nonsingular matrix A has been considered by different authors for the classes of M—matrices, positive definite matrices and totally positive (negative) matrices. This problem appears to be difficult as the results have been done only for matrices of order three. In this work, we continue to give the characterization of the diagonal entries of the combined matrix of the remainder sign regular matrices. Thus, the problem is closed for all possible sign regular matrices of order three.


Mathematics ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 962 ◽  
Author(s):  
Zhien Li ◽  
Chao Wang ◽  
Ravi P. Agarwal

In this paper, the non-eigenvalue forms of Liouville’s formulas for delta, nabla and α -diamond matrix dynamic equations on time scales are given and proved. Meanwhile, a diamond matrix exponential function (or α -matrix exponential function) is introduced and some classes of homogenous linear diamond- α dynamic equations which possess the α -matrix exponential solutions is studied. The difference and relation of non-eigenvalue forms of Liouville’s formulas among these representative types of dynamic equations is investigated. Moreover, we establish some sufficient conditions to guarantee transformational relation of Liouville’s formulas and exponential solutions among these types of matrix dynamic equations. In addition, we provide several examples on various time scales to illustrate the effectiveness of our result.


2019 ◽  
Vol 52 ◽  
pp. 885-894 ◽  
Author(s):  
Ángela Aguilar-de-Leyva ◽  
Maria Dolores Campiñez ◽  
Flavia Jost ◽  
Miguel Gavira ◽  
Isidoro Caraballo

Here MAGDM problems are explored. Attribute weight data given are in the form of problems involving numerical method solutions. The decision information during this study is in the shape of Intuitionistic Fuzzy Numbers (IFNs) derived from Intuitionistic Fuzzy Sets (IFSs). The IFOWA operator and IFHA operator are used for collecting the combined matrix. The modified Euler-Cauchy method and Heun method are used to calculate the unidentified weights. Effectiveness of the projected method is established using Numerical Illustrations.


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