Biscogniauxia Granmoi (Xylariaceae) in Europe

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Pru Nus Contains Many Species and Cultivars, Pru Nus Including Both Fruits and Woody Ornamentals

;J. N l\J d.000 A~ :J-6 '. AGRICULTURAL EXTENSION SERVICE UNIVERSITY OF MINNESOTA • The genus Pru nus contains many species and cultivars, Pru nus including both fruits and woody ornamentals. The arboretum's Prunus maacki (Amur Cherry). This small tree has bright, emphasis is on the ornamental plants. brownish-yellow bark that flakes off in papery strips. It is par Prunus americana (American Plum). This small tree furnishes ticularly attractive in winter when the stems contrast with the fruits prized for making preserves and is also an ornamental. snow. The flowers and fruits are produced in drooping racemes In early May, the trees are covered with a "snowball" bloom similar to those of our native chokecherry. This plant is ex of white flowers. If these blooms escape the spring frosts, tremely hardy and well worth growing. there will be a crop of colorful fruits in the fall. The trees Prunus maritima (Beach Plum). This species is native to the sucker freely, and unless controlled, a thicket results. The A coastal plains from Maine to Virginia. It's a sprawling shrub merican Plum is excellent for conservation purposes, and the reaching a height of about 6 feet. It blooms early with small thickets are favorite refuges for birds and wildlife. white flowers. Our plants have shown varying degrees of die Prunus amygdalus (Almond). Several cultivars of almonds back and have been removed for this reason. including 'Halls' and 'Princess'-have been tested. Although Prunus 'Minnesota Purple.' This cultivar was named by the the plants survived and even flowered, each winter's dieback University of Minnesota in 1920.
Phylogenetic Assignment of the Fungicolous Hypoxylon Invadens (Ascomycota, Xylariales) and Investigation of Its Secondary Metabolites

microorganisms Article Phylogenetic Assignment of the Fungicolous Hypoxylon invadens (Ascomycota, Xylariales) and Investigation of its Secondary Metabolites Kevin Becker 1,2 , Christopher Lambert 1,2,3 , Jörg Wieschhaus 1 and Marc Stadler 1,2,* 1 Department of Microbial Drugs, Helmholtz Centre for Infection Research GmbH (HZI), Inhoffenstraße 7, 38124 Braunschweig, Germany; [email protected] (K.B.); [email protected] (C.L.); [email protected] (J.W.) 2 German Centre for Infection Research Association (DZIF), Partner site Hannover-Braunschweig, Inhoffenstraße 7, 38124 Braunschweig, Germany 3 Department for Molecular Cell Biology, Helmholtz Centre for Infection Research GmbH (HZI) Inhoffenstraße 7, 38124 Braunschweig, Germany * Correspondence: [email protected]; Tel.: +49-531-6181-4240; Fax: +49-531-6181-9499 Received: 23 July 2020; Accepted: 8 September 2020; Published: 11 September 2020 Abstract: The ascomycete Hypoxylon invadens was described in 2014 as a fungicolous species growing on a member of its own genus, H. fragiforme, which is considered a rare lifestyle in the Hypoxylaceae. This renders H. invadens an interesting target in our efforts to find new bioactive secondary metabolites from members of the Xylariales. So far, only volatile organic compounds have been reported from H. invadens, but no investigation of non-volatile compounds had been conducted. Furthermore, a phylogenetic assignment following recent trends in fungal taxonomy via a multiple sequence alignment seemed practical. A culture of H. invadens was thus subjected to submerged cultivation to investigate the produced secondary metabolites, followed by isolation via preparative chromatography and subsequent structure elucidation by means of nuclear magnetic resonance (NMR) spectroscopy and high-resolution mass spectrometry (HR-MS).
Chokecherry Prunus Virginiana L

chokecherry Prunus virginiana L. Synonyms: Prunus virginiana ssp. demissa (Nutt.) Roy L. Taylor & MacBryde, P. demissa (Nutt.) Walp. Other common names: black chokecherry, bitter-berry, cabinet cherry, California chokecherry, caupulin, chuckleyplum, common chokecherry, eastern chokecherry, jamcherry, red chokecherry, rum chokecherry, sloe tree, Virginia chokecherry, western chokecherry, whiskey chokecherry, wild blackcherry, wild cherry Family: Rosaceae Invasiveness Rank: 74 The invasiveness rank is calculated based on a species’ ecological impacts, biological attributes, distribution, and response to control measures. The ranks are scaled from 0 to 100, with 0 representing a plant that poses no threat to native ecosystems and 100 representing a plant that poses a major threat to native ecosystems. Description Similar species: Several non-native Prunus species can Chokecherry is a deciduous, thicket-forming, erect shrub be confused with chokecherry in Alaska. Unlike or small tree that grows 1 to 6 m tall from an extensive chokecherry, which has glabrous inner surfaces of the network of lateral roots. Roots can extend more than 10 basal sections of the flowers, European bird cherry m horizontally and 2 m vertically. Young twigs are often (Prunus padus) has hairy inner surfaces of the basal hairy. Stems are numerous, slender, and branched. Bark sections of the flowers. Chokecherry can also be is smooth to fine-scaly and red-brown to grey-brown. differentiated from European bird cherry by its foliage, Leaves are alternate, elliptic to ovate, and 3 to 10 cm which turns red in late summer and fall; the leaves of long with pointed tips and toothed margins. Upper European bird cherry remain green throughout the surfaces are green and glabrous, and lower surfaces are summer.
Resurrection and Emendation of the Hypoxylaceae, Recognised from a Multigene Phylogeny of the Xylariales

Mycol Progress DOI 10.1007/s11557-017-1311-3 ORIGINAL ARTICLE Resurrection and emendation of the Hypoxylaceae, recognised from a multigene phylogeny of the Xylariales Lucile Wendt1,2 & Esteban Benjamin Sir3 & Eric Kuhnert1,2 & Simone Heitkämper1,2 & Christopher Lambert1,2 & Adriana I. Hladki3 & Andrea I. Romero4,5 & J. Jennifer Luangsa-ard6 & Prasert Srikitikulchai6 & Derek Peršoh7 & Marc Stadler1,2 Received: 21 February 2017 /Revised: 12 April 2017 /Accepted: 19 April 2017 # The Author(s) 2017. This article is an open access publication Abstract A multigene phylogeny was constructed, including polymerase II (RPB2), and beta-tubulin (TUB2). Specimens a significant number of representative species of the main were selected based on more than a decade of intensive mor- lineages in the Xylariaceae and four DNA loci the internal phological and chemotaxonomic work, and cautious taxon transcribed spacer region (ITS), the large subunit (LSU) of sampling was performed to cover the major lineages of the the nuclear rDNA, the second largest subunit of the RNA Xylariaceae; however, with emphasis on hypoxyloid species. The comprehensive phylogenetic analysis revealed a clear-cut This article is part of the “Special Issue on ascomycete systematics in segregation of the Xylariaceae into several major clades, honor of Richard P. Korf who died in August 2016”. which was well in accordance with previously established morphological and chemotaxonomic concepts. One of these The present paper is dedicated to Prof. Jack D. Rogers, on the occasion of his fortcoming 80th birthday. clades contained Annulohypoxylon, Hypoxylon, Daldinia,and other related genera that have stromatal pigments and a Section Editor: Teresa Iturriaga and Marc Stadler nodulisporium-like anamorph.
Bceccarelli Tesid.Pdf

A tutti quelli che aspettano l’ora della loro vita... "Dilige, et quod vis fac: sive taceas, dilectione taceas; sive clames, dilectione clames; sive emendes, dilectione emendes; sive parcas, dilectione parcas: radix sit intus dilectionis, non potest de ista radice nisi bonum existere". Sant'Agostino (In Io. Ep. tr. 7, 8) Abstract This thesis has investigated diversity and distribution of "pathogenic" and "non-pathogenic" fungal endophyte communities in twigs, leaves and buds of Fagus sylvatica in beech Italian forest into Monte Cimino area. In last decade European beech has been subject to a number of biotic and abiotic stresses included the increasing impact of drought and, as a consequence, the impact of native parasites that attack weakened hosts. Among these, Biscogniauxia nummularia (Bull.) Kuntze, associated with severe beech- declines, has been studied for its importance as latent pathogen of healthy beech tissues. Understanding how fungal endophyte communities differ in abundance, diversity and taxonomic composition is key to understanding the ecology and evolutionary context of endophyte-plant associations. Fungal ITS sequences were used for validation of morphological identification and phylogenetic analysis. According to the ITS phylogeny, endophytes studied belong to the main non-parasitic and non-lichenised orders of Pezizomycotina. The effects of native tissue, site exposure, and season on endophyte assemblages were investigated. Native tissue was the major factor shaping endophyte assemblages. Exposure and seasonal differences played a significant but lesser role. Several recently developed molecular methods offer new tools for determining the presence and diversity of fungi in complex microbial communities. Terminal restriction fragment (TRF) pattern analysis was tested as a method for assessing the molecular diversity of endophyte fungal community within asymptomatic beech tissues.
Table of Contents

Table of Contents Table of Contents ............................................................................................................ 1 Authors, Reviewers, Draft Log ........................................................................................ 3 Introduction to Reference ................................................................................................ 5 Introduction to Stone Fruit ............................................................................................. 10 Arthropods ................................................................................................................... 16 Primary Pests of Stone Fruit (Full Pest Datasheet) ....................................................... 16 Adoxophyes orana ................................................................................................. 16 Bactrocera zonata .................................................................................................. 27 Enarmonia formosana ............................................................................................ 39 Epiphyas postvittana .............................................................................................. 47 Grapholita funebrana ............................................................................................. 62 Leucoptera malifoliella ........................................................................................... 72 Lobesia botrana ....................................................................................................
The Ornamental Trees of South Dakota N.E

South Dakota State University Open PRAIRIE: Open Public Research Access Institutional Repository and Information Exchange South Dakota State University Agricultural Bulletins Experiment Station 4-1-1931 The Ornamental Trees of South Dakota N.E. Hansen Follow this and additional works at: http://openprairie.sdstate.edu/agexperimentsta_bulletins Recommended Citation Hansen, N.E., "The Ornamental Trees of South Dakota" (1931). Bulletins. Paper 260. http://openprairie.sdstate.edu/agexperimentsta_bulletins/260 This Bulletin is brought to you for free and open access by the South Dakota State University Agricultural Experiment Station at Open PRAIRIE: Open Public Research Access Institutional Repository and Information Exchange. It has been accepted for inclusion in Bulletins by an authorized administrator of Open PRAIRIE: Open Public Research Access Institutional Repository and Information Exchange. For more information, please contact [email protected]. Bulletin 260 April, 1931 The Ornamental Trees of South Dakota Figure I-The May Day Tree. Horticulture Department Agricultural Experiment Station South Dakota State College of Agriculture and Mechanic Arts Brookings, S. Dak. The Ornamental Trees of South Dakota N. E. Hansen This bulletin describes the deciduous trees. By deciduous trees is meant those that shed their leaves in winter. The evergreens of South Dakota are described in bulletin 254, October 1930. A bulletin on "The Ornamental Shrubs of South Dakota" is ready for early publication. The following list should be studied in connection with the trees described in South Dakota bulletin 246, "'The Shade, Windbreak and Timber Trees of South Dakota," 48 pages, March 1930. All the trees in both bulletins have ornamental value in greater or less degree.
Alaska Region Pathways Animal Introductions Alaska Has a Long History of Animal Tricia L

This work was supported in part by the U.S. Department of Agriculture, Forest Service. The findings and conclusions in this publication are those of the authors and should not be 336 construed to represent any official USDA or U.S. Government determination or policy. Appendix: Regional Summaries Alaska Region Pathways Animal Introductions Alaska has a long history of animal Tricia L. Wurtz and Bethany K. Schulz introductions, especially on its islands (Bailey 1993; Paul 2009). The frst deliberate releases of Arctic foxes (Vulpes Introduction lagopus) for fox ranching on several Aleutian Islands Alaska has fewer invasive species and is less impacted by occurred in 1750 (Black 1984); the frst known accidental invasive species than most places on Earth. Until recently, release of Norway rats (Rattus norvegicus) was prior to 1780 Alaska has been protected by its cold climate and by its via a shipwreck (Brechbill 1977). The rats spread so comparative lack of roads and other development. prolifcally that the island where the shipwreck occurred However, these barriers are eroding. Warming climate later came to be known as Rat Island (Ebbert and Byrd 2002). trends and longer shoulder seasons have reduced the cli- It was the site of an intensive, successful rat eradication mate flter that so far may have prevented some invasive effort in 2008 for the purpose of restoring seabird nesting species from establishing in the State (Figs. A1.1 and A1.2; habitat (Croll et al. 2016; Dunham 2012; Fritts 2007; USFWS Carlson et al. 2015; Jarnevich et al. 2014; Sanderson et al. 2007). Cattle (Bos taurus), Sitka black-tailed deer 2012; Wolken et al.
<I>Acrocordiella</I>

Persoonia 37, 2016: 82–105 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158516X690475 Resolution of morphology-based taxonomic delusions: Acrocordiella, Basiseptospora, Blogiascospora, Clypeosphaeria, Hymenopleella, Lepteutypa, Pseudapiospora, Requienella, Seiridium and Strickeria W.M. Jaklitsch1,2, A. Gardiennet3, H. Voglmayr2 Key words Abstract Fresh material, type studies and molecular phylogeny were used to clarify phylogenetic relationships of the nine genera Acrocordiella, Blogiascospora, Clypeosphaeria, Hymenopleella, Lepteutypa, Pseudapiospora, Ascomycota Requienella, Seiridium and Strickeria. At first sight, some of these genera do not seem to have much in com- Dothideomycetes mon, but all were found to belong to the Xylariales, based on their generic types. Thus, the most peculiar finding new genus is the phylogenetic affinity of the genera Acrocordiella, Requienella and Strickeria, which had been classified in phylogenetic analysis the Dothideomycetes or Eurotiomycetes, to the Xylariales. Acrocordiella and Requienella are closely related but pyrenomycetes distinct genera of the Requienellaceae. Although their ascospores are similar to those of Lepteutypa, phylogenetic Pyrenulales analyses do not reveal a particularly close relationship. The generic type of Lepteutypa, L. fuckelii, belongs to the Sordariomycetes Amphisphaeriaceae. Lepteutypa sambuci is newly described. Hymenopleella is recognised as phylogenetically Xylariales distinct from Lepteutypa, and Hymenopleella hippophaëicola is proposed as new name for its generic type, Spha eria (= Lepteutypa) hippophaës. Clypeosphaeria uniseptata is combined in Lepteutypa. No asexual morphs have been detected in species of Lepteutypa. Pseudomassaria fallax, unrelated to the generic type, P. chondrospora, is transferred to the new genus Basiseptospora, the genus Pseudapiospora is revived for P. corni, and Pseudomas saria carolinensis is combined in Beltraniella (Beltraniaceae).
Secondary Metabolites from the Genus Xylaria and Their Bioactivities

CHEMISTRY & BIODIVERSITY – Vol. 11 (2014) 673 REVIEW Secondary Metabolites from the Genus Xylaria and Their Bioactivities by Fei Song, Shao-Hua Wu*, Ying-Zhe Zhai, Qi-Cun Xuan, and Tang Wang Key Laboratory for Microbial Resources of the Ministry of Education, Yunnan Institute of Microbiology, Yunnan University, Kunming 650091, P. R. China (phone: þ86-871-65032423; e-mail: [email protected]) Contents 1. Introduction 2. Secondary Metabolites 2.1. Sesquiterpenoids 2.1.1. Eremophilanes 2.1.2. Eudesmanolides 2.1.3. Presilphiperfolanes 2.1.4. Guaianes 2.1.5. Brasilanes 2.1.6. Thujopsanes 2.1.7. Bisabolanes 2.1.8. Other Sesquiterpenes 2.2. Diterpenoids and Diterpene Glycosides 2.3. Triterpene Glycosides 2.4. Steroids 2.5. N-Containing Compounds 2.5.1. Cytochalasins 2.5.2. Cyclopeptides 2.5.3. Miscellaneous Compounds 2.6. Aromatic Compounds 2.6.1. Xanthones 2.6.2. Benzofuran Derivatives 2.6.3. Benzoquinones 2.6.4. Coumarins and Isocoumarins 2.6.5. Chroman Derivatives 2.6.6. Naphthalene Derivatives 2.6.7. Anthracenone Derivatives 2.6.8. Miscellaneous Phenolic Derivatives 2.7. Pyranone Derivatives 2.8. Polyketides 3. Biological Activities 3.1. Antimicrobial Activity 3.2. Antimalarial Activity 2014 Verlag Helvetica Chimica Acta AG, Zrich 674 CHEMISTRY & BIODIVERSITY – Vol. 11 (2014) 3.3. Cytotoxic Activity 3.4. Other Activities 4. Conclusions 1. Introduction. – Xylaria Hill ex Schrank is the largest genus of the family Xylariaceae Tul.&C.Tul. (Xylariales, Sordariomycetes) and presently includes ca. 300 accepted species of stromatic pyrenomycetes [1]. Xylaria species are widespread from the temperate to the tropical zones of the earth [2].
Dimensions of Biodiversity

Dimensions of Biodiversity NATIONAL SCIENCE FOUNDATION CO-FUNDED BY 2010–2015 PROJECTS Introduction 4 Project Abstracts 2015 8 Project Updates 2014 30 Project Updates 2013 42 Project Updates 2012 56 Project Updates 2011 72 Project Updates 2010 88 FRONT COVER IMAGES A B f g h i k j C l m o n q p r D E IMAGE CREDIT THIS PAGE FRONT COVER a MBARI & d Steven Haddock f Steven Haddock k Steven Haddock o Carolyn Wessinger Peter Girguis e Carolyn g Erin Tripp l Lauren Schiebelhut p Steven Litaker b James Lendemer Wessinger h Marty Condon m Lawrence Smart q Sahand Pirbadian & c Matthew L. Lewis i Marty Condon n Verity Salmon Moh El-Naggar j Niklaus Grünwald r Marty Condon FIELD SITES Argentina France Singapore Australia French Guiana South Africa Bahamas French Polynesia Suriname Belize Germany Spain Bermuda Iceland Sweden Bolivia Japan Switzerland Brazil Madagascar Tahiti Canada Malaysia Taiwan China Mexico Thailand Colombia Norway Trinidad Costa Rica Palau United States Czech Republic Panama United Kingdom Dominican Peru Venezuela Republic Philippines Labrador Sea Ecuador Poland North Atlantic Finland Puerto Rico Ocean Russia North Pacific Ocean Saudi Arabia COLLABORATORS Argentina Finland Palau Australia France Panama Brazil Germany Peru Canada Guam Russia INTERNATIONAL PARTNERS Chile India South Africa China Brazil China Indonesia Sri Lanka (NSFC) (FAPESP) Colombia Japan Sweden Costa Rica Kenya United Denmark Malaysia Kingdom Ecuador Mexico ACKNOWLEDGMENTS Many NSF staff members, too numerous to We thank Mina Ta and Matthew Pepper for mention individually, assisted in the development their graphic design contribution to the abstract and implementation of the Dimensions of booklet.
Taxonomic Re-Examination of Nine Rosellinia Types (Ascomycota, Xylariales) Stored in the Saccardo Mycological Collection

microorganisms Article Taxonomic Re-Examination of Nine Rosellinia Types (Ascomycota, Xylariales) Stored in the Saccardo Mycological Collection Niccolò Forin 1,* , Alfredo Vizzini 2, Federico Fainelli 1, Enrico Ercole 3 and Barbara Baldan 1,4,* 1 Botanical Garden, University of Padova, Via Orto Botanico, 15, 35123 Padova, Italy; [email protected] 2 Institute for Sustainable Plant Protection (IPSP-SS Torino), C.N.R., Viale P.A. Mattioli, 25, 10125 Torino, Italy; [email protected] 3 Department of Life Sciences and Systems Biology, University of Torino, Viale P.A. Mattioli, 25, 10125 Torino, Italy; [email protected] 4 Department of Biology, University of Padova, Via Ugo Bassi, 58b, 35131 Padova, Italy * Correspondence: [email protected] (N.F.); [email protected] (B.B.) Abstract: In a recent monograph on the genus Rosellinia, type specimens worldwide were revised and re-classiﬁed using a morphological approach. Among them, some came from Pier Andrea Saccardo’s fungarium stored in the Herbarium of the Padova Botanical Garden. In this work, we taxonomically re-examine via a morphological and molecular approach nine different Rosellinia sensu Saccardo types. ITS1 and/or ITS2 sequences were successfully obtained applying Illumina MiSeq technology and phylogenetic analyses were carried out in order to elucidate their current taxonomic position. Only the Citation: Forin, N.; Vizzini, A.; ITS1 sequence was recovered for Rosellinia areolata, while for R. geophila, only the ITS2 sequence was Fainelli, F.; Ercole, E.; Baldan, B. recovered. We proposed here new combinations for Rosellinia chordicola, R. geophila and R. horridula, Taxonomic Re-Examination of Nine R. ambigua R.