Indicis Nominum Familiarum Angiospermarum Prodromus A
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Toward a Resolution of Campanulid Phylogeny, with Special Reference to the Placement of Dipsacales
TAXON 57 (1) • February 2008: 53–65 Winkworth & al. • Campanulid phylogeny MOLECULAR PHYLOGENETICS Toward a resolution of Campanulid phylogeny, with special reference to the placement of Dipsacales Richard C. Winkworth1,2, Johannes Lundberg3 & Michael J. Donoghue4 1 Departamento de Botânica, Instituto de Biociências, Universidade de São Paulo, Caixa Postal 11461–CEP 05422-970, São Paulo, SP, Brazil. [email protected] (author for correspondence) 2 Current address: School of Biology, Chemistry, and Environmental Sciences, University of the South Pacific, Private Bag, Laucala Campus, Suva, Fiji 3 Department of Phanerogamic Botany, The Swedish Museum of Natural History, Box 50007, 104 05 Stockholm, Sweden 4 Department of Ecology & Evolutionary Biology and Peabody Museum of Natural History, Yale University, P.O. Box 208106, New Haven, Connecticut 06520-8106, U.S.A. Broad-scale phylogenetic analyses of the angiosperms and of the Asteridae have failed to confidently resolve relationships among the major lineages of the campanulid Asteridae (i.e., the euasterid II of APG II, 2003). To address this problem we assembled presently available sequences for a core set of 50 taxa, representing the diver- sity of the four largest lineages (Apiales, Aquifoliales, Asterales, Dipsacales) as well as the smaller “unplaced” groups (e.g., Bruniaceae, Paracryphiaceae, Columelliaceae). We constructed four data matrices for phylogenetic analysis: a chloroplast coding matrix (atpB, matK, ndhF, rbcL), a chloroplast non-coding matrix (rps16 intron, trnT-F region, trnV-atpE IGS), a combined chloroplast dataset (all seven chloroplast regions), and a combined genome matrix (seven chloroplast regions plus 18S and 26S rDNA). Bayesian analyses of these datasets using mixed substitution models produced often well-resolved and supported trees. -
Early Evolution of the Angiosperm Clade Asteraceae in the Cretaceous of Antarctica
Early evolution of the angiosperm clade Asteraceae in the Cretaceous of Antarctica Viviana D. Barredaa,1,2, Luis Palazzesia,b,1, Maria C. Telleríac, Eduardo B. Oliverod, J. Ian Rainee, and Félix Forestb aDivisión Paleobotánica, Museo Argentino de Ciencias Naturales “Bernardino Rivadavia,” Consejo Nacional de Investigaciones Cientificas y Técnicas, Buenos Aires C1405DJR, Argentina; bJodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, United Kingdom; cLaboratorio de Sistemática y Biología Evolutiva, Museo de La Plata, La Plata B1900FWA, Argentina; dCentro Austral de Investigaciones Científicas, Consejo Nacional de Investigaciones Cientificas y Técnicas, 9410 Ushuaia, Tierra del Fuego, Argentina; and eDepartment of Palaeontology, GNS Science, Lower Hutt 5040, New Zealand Edited by Michael J. Donoghue, Yale University, New Haven, CT, and approved July 15, 2015 (received for review December 10, 2014) The Asteraceae (sunflowers and daisies) are the most diverse Here we report fossil pollen evidence from exposed Campanian/ family of flowering plants. Despite their prominent role in extant Maastrichtian sediments from the Antarctic Peninsula (Fig. 1, Fig. S1, terrestrial ecosystems, the early evolutionary history of this family and SI Materials and Methods, Fossiliferous Localities)(7)thatradi- remains poorly understood. Here we report the discovery of a cally changes our understanding of the early evolution of Asteraceae. number of fossil pollen grains preserved in dinosaur-bearing deposits from the Late Cretaceous of Antarctica that drastically pushes back Results and Discussion the timing of assumed origin of the family. Reliably dated to ∼76–66 The pollen grains reported here and discovered in the Late Cre- Mya, these specimens are about 20 million years older than previ- taceous of Antarctica are tricolporate, microechinate, with long ously known records for the Asteraceae. -
Alphabetical Lists of the Vascular Plant Families with Their Phylogenetic
Colligo 2 (1) : 3-10 BOTANIQUE Alphabetical lists of the vascular plant families with their phylogenetic classification numbers Listes alphabétiques des familles de plantes vasculaires avec leurs numéros de classement phylogénétique FRÉDÉRIC DANET* *Mairie de Lyon, Espaces verts, Jardin botanique, Herbier, 69205 Lyon cedex 01, France - [email protected] Citation : Danet F., 2019. Alphabetical lists of the vascular plant families with their phylogenetic classification numbers. Colligo, 2(1) : 3- 10. https://perma.cc/2WFD-A2A7 KEY-WORDS Angiosperms family arrangement Summary: This paper provides, for herbarium cura- Gymnosperms Classification tors, the alphabetical lists of the recognized families Pteridophytes APG system in pteridophytes, gymnosperms and angiosperms Ferns PPG system with their phylogenetic classification numbers. Lycophytes phylogeny Herbarium MOTS-CLÉS Angiospermes rangement des familles Résumé : Cet article produit, pour les conservateurs Gymnospermes Classification d’herbier, les listes alphabétiques des familles recon- Ptéridophytes système APG nues pour les ptéridophytes, les gymnospermes et Fougères système PPG les angiospermes avec leurs numéros de classement Lycophytes phylogénie phylogénétique. Herbier Introduction These alphabetical lists have been established for the systems of A.-L de Jussieu, A.-P. de Can- The organization of herbarium collections con- dolle, Bentham & Hooker, etc. that are still used sists in arranging the specimens logically to in the management of historical herbaria find and reclassify them easily in the appro- whose original classification is voluntarily pre- priate storage units. In the vascular plant col- served. lections, commonly used methods are systema- Recent classification systems based on molecu- tic classification, alphabetical classification, or lar phylogenies have developed, and herbaria combinations of both. -
Amaryllis – Hardy Scientific Name: Hippeastrum Johnsoni Common
Name: Amaryllis – Hardy Scientific name: Hippeastrum johnsoni Common Names: Cluster Amaryllis, Hurricane Lily, Magic Lily, Spider Lily, Stone Garlic. Life Cycle: Hardy bulb. Height: 12 to 36 inches (30 to 90 cm). Native: Asia. Growing Region: Zones 7 to 10. Flowers: Late summer through to autumn. Flower Details: White, red, pink, orange, yellow. Lily- like. Umbel; four to eight flowers. Foliage: Slender. Long. Grow Outside: Usually grown from bulbs or vegetatively propagated plants as seed grown plants can take up to 12 years to bloom. Bulbs: 3 to 8 inches (8 to 20 cm) depending upon species. End of summer Requirements and care: Full sunlight or partial shade. Good drainage. Acidic to neutral soil. Rich soil, moist soil. Regular watering to maintain soil moisture. Requires a feed every two years; do this during the growing season. Propagate: by planting bulblets once blooming has finished. Source: http://www.plant-biology.com/Lycoris-Hardy-Amaryllis.php http://www.brecksbulbs.ca/product/Hardy-Amaryllis-Mixture/Summer_Bulbs Extension programs service people of all ages regardless of socioeconomic level, race, color, sex, religion, disability, or national origin. The Texas A&M University System, U.S. Department of Agriculture, and the County Commissioners Courts of Texas Cooperating A member of The Texas A&M University System and its statewide Agriculture Program. Common Name: Artemesia - Powis Castle Botanical name: Artemesiax Powis Castle Plant Type: Perennial Light Requirement: High Water Requirement: Low Hardiness/Zone: 4 - 8 Heat/Drought Tolerance: High Height: 3 ft Width/Spacing: 3ft Flower Color: Yellow Blooming Period: Rarely flowers Plant Form or Habit: Evergreen woody perennial, or shrub Foliage Color and Texture: Leaves are finely dissected like filigreed silver lacework. -
Complete Chloroplast Genomes Shed Light on Phylogenetic
www.nature.com/scientificreports OPEN Complete chloroplast genomes shed light on phylogenetic relationships, divergence time, and biogeography of Allioideae (Amaryllidaceae) Ju Namgung1,4, Hoang Dang Khoa Do1,2,4, Changkyun Kim1, Hyeok Jae Choi3 & Joo‑Hwan Kim1* Allioideae includes economically important bulb crops such as garlic, onion, leeks, and some ornamental plants in Amaryllidaceae. Here, we reported the complete chloroplast genome (cpDNA) sequences of 17 species of Allioideae, fve of Amaryllidoideae, and one of Agapanthoideae. These cpDNA sequences represent 80 protein‑coding, 30 tRNA, and four rRNA genes, and range from 151,808 to 159,998 bp in length. Loss and pseudogenization of multiple genes (i.e., rps2, infA, and rpl22) appear to have occurred multiple times during the evolution of Alloideae. Additionally, eight mutation hotspots, including rps15-ycf1, rps16-trnQ-UUG, petG-trnW-CCA , psbA upstream, rpl32- trnL-UAG , ycf1, rpl22, matK, and ndhF, were identifed in the studied Allium species. Additionally, we present the frst phylogenomic analysis among the four tribes of Allioideae based on 74 cpDNA coding regions of 21 species of Allioideae, fve species of Amaryllidoideae, one species of Agapanthoideae, and fve species representing selected members of Asparagales. Our molecular phylogenomic results strongly support the monophyly of Allioideae, which is sister to Amaryllioideae. Within Allioideae, Tulbaghieae was sister to Gilliesieae‑Leucocoryneae whereas Allieae was sister to the clade of Tulbaghieae‑ Gilliesieae‑Leucocoryneae. Molecular dating analyses revealed the crown age of Allioideae in the Eocene (40.1 mya) followed by diferentiation of Allieae in the early Miocene (21.3 mya). The split of Gilliesieae from Leucocoryneae was estimated at 16.5 mya. -
Narcissus Pests
Bulletin 51 HMSO 13s Od [65p] net Narcissus Pests Ministry of Agriculture, Fisheries and Food MINISTRY OF AGRICULTURE, FISHERIES AND FOOD Narcissus Pests Bulletin 51 LONDON HER MAJESTY'S STATIONERY OFFICE 197o First published June 1932 Sixth edition 197o The Ministry does not accept responsibility for any of the private or trade advertisements included in this publication. SBN 11 240351 4 Foreword THE growers of Narcissus have been very fortunate in that the pests of this valuable crop have received specialist attention for nearly forty years. Names like W. E. H. Hodson and L. N. Staniland, both past authors of this Bulletin, rank high in the list of pioneer researchers on bulb pests in this country. They have been followed with no less enthusiasm by the con- tributors to this sixth edition which brings up-to-date our knowledge of the important pests of the crop and tested and practical methods of control. Although the present Bulletin mainly follows the pattern laid down by Mr. Hodson in 1932 many sections have been extensively rewritten. Mr. H. C. Woodville has dealt with narcissus flies as he did in 1958, and Mr. H. G. Morgan with detection of pests in the field, stem and other eelworms and their control. Mr. A. L. Winfield covered bulb scale mite and the general problem of hot-water treatment of bulbs, and chemical dips to control stem eelworm, and also contributed the notes on miscellaneous pests. Mr. P. Aitkenhead dealt with bulb mites. Mr. J. F. Southey provided the section dealing with eelworms as vectors of virus diseases of the crop. -
Poranthera Microphylla
Plants of South Eastern New South Wales Flowering stems. Australian Plant Image Index, photographer Murray Fagg, near Cabrumurra Flowering plant. Photographer Don Wood, Namadgi National Park, ACT Flowering stems. Photographer Don Wood, Namadgi Line drawings. b. seed case; flowering branch; male National Park, ACT flower. E Mayfield, National Herbarium of Victoria, © 2021 Royal Botanic Gardens Board Common name Small poranthera Family Phyllanthaceae Where found Forest, woodland, heath, grassy areas, and roadsides. Widespread. Notes Annual herb to 0.2 m tall or sprawling, hairless, sometimes somewhat glaucous. Leaves opposite each other to alternating up the stems, 0.2-1.6 cm long, 1-5 mm wide, flattish in cross section, hairless, sometimes somewhat glaucous, margins slightly curved down or sometimes flat, tips blunt, usually with a short point. Male and female flowers on the same plant. Flowers with 5 white, green, or pink sepals each 0.4-1.5 mm long, and 5 white, pink, or pale mauve petals 0.2-0.6 mm long. Petals sometimes 0 in female flowers. Flowers in clusters 3-8 mm in diameter. Flowers most of the year. Family was Euphorbiaceae. All native plants on unleased land in the ACT are protected. The description above is partly taken from Halford, D.A. & Henderson, R.J.F. (2005) Studies in Euphorbiaceae, s. lat. 6. A revision of the genus Poranthera Rudge (Antidesmeae, Porantherinae) in Australia. Austrobaileya 7 (1): pages 16-19. PlantNET description: http://plantnet.rbgsyd.nsw.gov.au/cgi-bin/NSWfl.pl? page=nswfl&lvl=sp&name=Poranthera~microphylla (accessed 2 February, 2021) Author: Betty Wood. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
Generic Classification of Amaryllidaceae Tribe Hippeastreae Nicolás García,1 Alan W
TAXON 2019 García & al. • Genera of Hippeastreae SYSTEMATICS AND PHYLOGENY Generic classification of Amaryllidaceae tribe Hippeastreae Nicolás García,1 Alan W. Meerow,2 Silvia Arroyo-Leuenberger,3 Renata S. Oliveira,4 Julie H. Dutilh,4 Pamela S. Soltis5 & Walter S. Judd5 1 Herbario EIF & Laboratorio de Sistemática y Evolución de Plantas, Facultad de Ciencias Forestales y de la Conservación de la Naturaleza, Universidad de Chile, Av. Santa Rosa 11315, La Pintana, Santiago, Chile 2 USDA-ARS-SHRS, National Germplasm Repository, 13601 Old Cutler Rd., Miami, Florida 33158, U.S.A. 3 Instituto de Botánica Darwinion, Labardén 200, CC 22, B1642HYD, San Isidro, Buenos Aires, Argentina 4 Departamento de Biologia Vegetal, Instituto de Biologia, Universidade Estadual de Campinas, Postal Code 6109, 13083-970 Campinas, SP, Brazil 5 Florida Museum of Natural History, University of Florida, Gainesville, Florida 32611, U.S.A. Address for correspondence: Nicolás García, [email protected] DOI https://doi.org/10.1002/tax.12062 Abstract A robust generic classification for Amaryllidaceae has remained elusive mainly due to the lack of unequivocal diagnostic characters, a consequence of highly canalized variation and a deeply reticulated evolutionary history. A consensus classification is pro- posed here, based on recent molecular phylogenetic studies, morphological and cytogenetic variation, and accounting for secondary criteria of classification, such as nomenclatural stability. Using the latest sutribal classification of Hippeastreae (Hippeastrinae and Traubiinae) as a foundation, we propose the recognition of six genera, namely Eremolirion gen. nov., Hippeastrum, Phycella s.l., Rhodolirium s.str., Traubia, and Zephyranthes s.l. A subgeneric classification is suggested for Hippeastrum and Zephyranthes to denote putative subclades. -
TELOPEA Publication Date: 13 October 1983 Til
Volume 2(4): 425–452 TELOPEA Publication Date: 13 October 1983 Til. Ro)'al BOTANIC GARDENS dx.doi.org/10.7751/telopea19834408 Journal of Plant Systematics 6 DOPII(liPi Tmst plantnet.rbgsyd.nsw.gov.au/Telopea • escholarship.usyd.edu.au/journals/index.php/TEL· ISSN 0312-9764 (Print) • ISSN 2200-4025 (Online) Telopea 2(4): 425-452, Fig. 1 (1983) 425 CURRENT ANATOMICAL RESEARCH IN LILIACEAE, AMARYLLIDACEAE AND IRIDACEAE* D.F. CUTLER AND MARY GREGORY (Accepted for publication 20.9.1982) ABSTRACT Cutler, D.F. and Gregory, Mary (Jodrell(Jodrel/ Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, England) 1983. Current anatomical research in Liliaceae, Amaryllidaceae and Iridaceae. Telopea 2(4): 425-452, Fig.1-An annotated bibliography is presented covering literature over the period 1968 to date. Recent research is described and areas of future work are discussed. INTRODUCTION In this article, the literature for the past twelve or so years is recorded on the anatomy of Liliaceae, AmarylIidaceae and Iridaceae and the smaller, related families, Alliaceae, Haemodoraceae, Hypoxidaceae, Ruscaceae, Smilacaceae and Trilliaceae. Subjects covered range from embryology, vegetative and floral anatomy to seed anatomy. A format is used in which references are arranged alphabetically, numbered and annotated, so that the reader can rapidly obtain an idea of the range and contents of papers on subjects of particular interest to him. The main research trends have been identified, classified, and check lists compiled for the major headings. Current systematic anatomy on the 'Anatomy of the Monocotyledons' series is reported. Comment is made on areas of research which might prove to be of future significance. -
Indigenous Plant Naming and Experimentation Reveal a Plant–Insect Relationship in New Zealand Forests
Received: 23 February 2020 Revised: 10 August 2020 Accepted: 25 August 2020 DOI: 10.1111/csp2.282 CONTRIBUTED PAPER Indigenous plant naming and experimentation reveal a plant–insect relationship in New Zealand forests Priscilla M. Wehi1,2 | Gretchen Brownstein2 | Mary Morgan-Richards1 1School of Agriculture and Environment, Massey University, Palmerston North, Abstract New Zealand Drawing from both Indigenous and “Western” scientific knowledge offers the 2Manaaki Whenua Landcare Research, opportunity to better incorporate ecological systems knowledge into conserva- Dunedin, New Zealand tion science. Here, we demonstrate a “two-eyed” approach that weaves Indige- Correspondence nous ecological knowledge (IK) with experimental data to provide detailed and Priscilla M. Wehi, Manaaki Whenua comprehensive information about regional plant–insect interactions in Landcare Research, 764 Cumberland New Zealand forests. We first examined Maori names for a common forest Street, Dunedin 9053, New Zealand. Email: [email protected], tree, Carpodetus serratus, that suggest a close species interaction between an [email protected] herbivorous, hole-dwelling insect, and host trees. We detected consistent – Funding information regional variation in both Maori names for C. serratus and the plant insect Foundation for Research, Science and relationship that reflect Hemideina spp. abundances, mediated by the presence Technology; Royal Society of New Zealand of a wood-boring moth species. We found that in regions with moths C. serratus trees are home to more weta than adjacent forest species and that these weta readily ate C. serratus leaves, fruits and seeds. These findings con- firm that a joint IK—experimental approach can stimulate new hypotheses and reveal spatially important ecological patterns. -
Pollen Ultrastructure of the Biovulate Euphorbiaceae Author(S): Michael G
Pollen Ultrastructure of the Biovulate Euphorbiaceae Author(s): Michael G. Simpson and Geoffrey A. Levin Reviewed work(s): Source: International Journal of Plant Sciences, Vol. 155, No. 3 (May, 1994), pp. 313-341 Published by: The University of Chicago Press Stable URL: http://www.jstor.org/stable/2475184 . Accessed: 26/07/2012 14:35 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. The University of Chicago Press is collaborating with JSTOR to digitize, preserve and extend access to International Journal of Plant Sciences. http://www.jstor.org Int.J. Plant Sci. 155(3):313-341.1994. ? 1994by The Universityof Chicago. All rightsreserved. 1058-5893/94/5503-0008$02.00 POLLENULTRASTRUCTURE OF THE BIOVULATE EUPHORBIACEAE MICHAEL G. SIMPSON AND GEOFFREY A. LEVIN' Departmentof Biology,San Diego StateUniversity, San Diego,California 92182-0057; and BotanyDepartment, San Diego NaturalHistory Museum, P.O. Box 1390,San Diego,California 92112 Pollenultrastructure of the biovulate Euphorbiaceae, including the subfamilies Phyllanthoideae and Oldfieldioideae,was investigatedwith light, scanning electron, and transmissionelectron microscopy. Pollenof Phyllanthoideae, represented by 12 speciesin ninegenera, was prolateto oblate,almost always 3-colporate,rarely 3-porate or pantoporate,and mostlywith reticulate, rarely baculate, echinate, or scabrate,sculpturing.