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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. -
An Antillean Plant of Beauty, a French Botanist, and a German Name: Naming Plants in the Early Modern Atlantic World
Estonian Journal of Ecology, 2012, 61, 1, 37–50 doi: 10.3176/eco.2012.1.05 An Antillean plant of beauty, a French botanist, and a German name: naming plants in the Early Modern Atlantic world Laura Hollsten Faculty of Arts, Åbo Akademi University, 20500 Åbo, Finland; [email protected] Received 10 December 2010, revised 7 March 2011, accepted 27 June 2011 Abstract. This paper investigates the naming of plants in the work of the French botanist Charles Plumier (1646–1704). Plumier made three trips to the French Antilles between 1690 and 1697, was appointed royal botanist in 1693, and published his first work, Description des Plantes de l’Amérique, in the same year. Plumier was the first ‘modern’ botanist to describe the flora of the Caribbean in a time when natural history underwent significant qualitative changes as a result of the European expansion and transatlantic contacts. Plumier’s ambition was to replace the confusing multitude of names given to New World plants with a universal taxonomically based nomenclature. His modernity and scientific ethos manifest themselves in his neutral way of organizing the plants according to a taxonomic system and his use of a Latin nomenclature, often naming plants after well-known botanists. Through Plumier’s naming process, I argue, it is possible to highlight the colonial and Atlantic context of his work, his network as part of the scientific elite of his country, and his professionalism resulting from years of botanical studies. Key words: history of botany, early modern natural history, plant nomenclature. INTRODUCTION According to a story entitled ‘The Tree of Riches’, the French botanist Charles Plumier decided that he would like to travel the world and get rich (Pellowski, 1990). -
Campanulaceae) Based on ITS and Tranl-F Sequence Data: Implications for a Reclassification
CORE Metadata, citation and similar papers at core.ac.uk Provided by University of the Western Cape Research Repository Cupido, C. N. et al. (2013). Phylogeny of Southern African and Australasian Wahlenbergioids (Campanulaceae) based on ITS and tranL-F sequence data: implications for a reclassification. Systematic Botany, 38(2): 523 – 535 http:// doi.org/10.1600/036364413X666714 dx. Phylogeny of Southern African and Australasian Wahlenbergioids (Campanulaceae) based on ITS and trnL-F sequence data: implications for a reclassification Christopher N. Cupido , Jessica M. Prebble , and William M. M. Eddie Abstract The Campanulaceae: Wahlenbergioideae currently comprises 15 genera, one of which, Wahlenbergia, is widespread over the southern continents. Southern Africa is the region with maximum wahlenbergioid diversity with 12 genera and approximately 252 species. A second center is Australasia with 38 Wahlenbergia species. This study used a broad sample of wahlenbergioid diversity from South Africa, Australia, and New Zealand to reconstruct a phylogeny based on chloroplast trnL-F and nuclear ITS sequences. Data were analyzed separately and in combination using parsimony and Bayesian methods. The results suggest that for the wahlenbergioids to be monophyletic Wahlenbergia hederacea has to be excluded and that none of the South African, Australian or New Zealand lineages are strictly monophyletic. There are five species assemblages that are in some disagreement with current classification in the family. Wahlenbergia, Prismatocarpus and Roella are shown to be non-monophyletic and implications for a reclassification are presented. Careful consideration of morphological characters is suggested before the adjustment of generic circumscriptions can be accomplished. Recent family-wide molecular phylogenetic studies have supported the view that the Campanulaceae s.s. -
Notes on Hawaiian Lobelioideae, with Descriptions of New Species and Varieties
v [From BULLETIN OF THE TORREY BOTANICAL CLUB. 44: 229-239.Pls. <rIb. 19 May 191 7.] Notes on Hawaiian Lobelioideae, with descriptions of new species and varieties JOSEPH F. ROCK (WITH PLATES 9-16) The writer has prepared a monograph on the Hawaiian lobelioi deous genera Cyanea, Rollandia, Clermontia, Delissea, Tremato lobelia and Brighamia, and on the endemic species of the genus Lo belia. But owing to the length of time necessary for the publica tion of the rather voluminous manuscript of the whole monograph, he thought itwise to publish the new species first in botanical peri odicals or bulletins. The majority of the new species of Cyanea and Clermontia have appeared in the writer's book on the In digenous Trees of the Hawaiian Islands (1913), in Bo.tanical Bul letin No.2, of the College of Hawaii Publications and in the Bul letin of the Torrey Botanical Club. With two exceptions the species and varieties described in the present paper belong to the genus Cyanea, which has by far the largest number of species of the lobelioideous genera represented in the Islands. Clermontia comes next, with RolZandia and Delissea following. I L I Cyanea noli-me-tangere sp. nov. II Plant subherbaceous, 3-20 dm. high, terrestrial, branching only when broken, spinescent throughout, with the exception of the fruit and corolla; stem green, somewhat fleshy, entirely i~ covered with strong, pale yellow, hollow spines; leaves bright ~ .green, ovate-oblong, somewhat acute at the apex, rounded at the I base, thin in texture, irregularly and sinuately notched, with Ii minute, mucronulate teeth along the margin, covered with yellow spines at more or less regular intervals of 7-10 mm. -
Chromosome Numbers of the East African Giant Senecios and Giant Lobelias and Their Evolutionary Significancei
American Journal of Botany 80(7): 847-853. 1993. CHROMOSOME NUMBERS OF THE EAST AFRICAN GIANT SENECIOS AND GIANT LOBELIAS AND THEIR EVOLUTIONARY SIGNIFICANCEI ERIC B. KNox2 AND ROBERT R, KOWAL Herbarium and Department of Biology, University of Michigan, Ann Arbor, Michigan 48109-1048; and Department of Botany, University of Wisconsin, Madison, Wisconsin 53706-1981 The gametophytic chromosome number for the giant senecios (Asteraceae, Senecioneae, Dendrosenecio) is n = 50, and for the giant lobelias (Lobeliaceae, Lobelia subgenus Tupa section Rhynchopetalumi it is n = 14. Previous sporophytic counts are generally verified, but earlier reports for the giant senecios of2n = 20 and ca. 80, the bases for claims ofintraspecific polyploidy, are unsubstantiated. The 14 new counts for the giant senecios and the ten new counts for the giant lobelias are the first garnetophytic records for these plants and include the first reports for six and four taxa, respectively, for the two groups. Only five of the II species of giant senecio and three of the 21 species of giant lobelia from eastern Africa remain uncounted. Although both groups are polyploid, the former presumably decaploid and the latter more certainly tetraploid, their adaptive radiations involved no further change in chromosome number. The cytological uniformity within each group, while providing circumstantial evidence ofmonophyly and simplifying interpretations ofcladistic analyses, provides neither positive nor negative support for a possible role of polyploidy in evolving the giant-rosette growth-form. Since their discovery last century, the giant senecios MATERIALS AND METHODS (Dendrosenecio; Nordenstam, 1978) and giant lobelias (Lobelia subgenus Tupa section Rhynchopetalum; Mab Excised anthers or very young flower buds of Lobelia berley, 1974b) of eastern Africa have attracted consid and immature heads of Dendrosenecio were fixed in the erable attention from taxonomists and evolutionary bi field in Carnoy's solution (3 chloroform: 2 absolute eth ologists (cf. -
Thorn-Like Prickles and Heterophyllyin Cyanea
Proc. Nadl. Acad. Sci. USA Vol. 91, pp. 2810-2814, March 1994 Evolution Thorn-like prickles and heterophylly in Cyanea: Adaptations to extinct avian browsers on Hawaii? (anti-herbivore ddenses/geese/leaf fonn/moa-nalos/paedomorphosis) T. J. GIVNISH*, K. J. SYTSMA, J. F. SMITHt, AND W. J. HAHNf Department of Botany, University of Wisconsin, Madison, WI 53706-1381 Communicated by Peter H. Raven, November 12, 1993 ABSTRACT The evolution of thorn-like structures in plants on oceanic islands that lack mammalian and reptilian herbivores is puzing, as is their tendency toward juvenile- adult leaf dimorphism. We propose that these traits arose in Cyanea (Campanul) on Hawaii as mechanical and visual defenses against herbivory by flightless geese and goose-like ducks that were extirated by Polynesians within the last 1600 years. A chloroplast DNA phylogeny indicates that thorn-like prickles evolved at least four times and leafdimorphism at least three times during the last 3.7 million years. The incidence of both traits increases from Oahu eastward toward younger islands, paralleling the dribution ofavian species apparently adapted for browsing. The effectiveness of visual defenses against avian browsers (once dominant on many oceanic is- lands, based on the vagility of their ancestors) may provide a general explanation for insar heterophylly: the other islands on which this previoul unexplained phenomenon is marked (New Zelnd, New Co a, Madagascar, Mascarene Is- lands) are exactly those on which one or more large ffightless avian browsers evolved. Cyanea (Campanulaceae: Lobelioideae), the largest genus of plants endemic to the Hawaiian archipelago, has undergone FiG. 1. Juvenile shoots of Cyanea solanacea on Molokai (Ka- striking adaptive radiations in growth form, leaf size and makoa Reserve, The Nature Conservancy), showing dense aggrega- shape, and floral morphology (1-5). -
Diversity of Wisconsin Asterids
Diversity of Wisconsin Asterids . bellflowers and asters . **Campanulaceae - bellflower family A family mostly of herbs, but some secondarily woody, widely distributed in the temperate regions and in the montane tropics. Contains 65 genera and over 2200 species, with half belonging to Campanula and Lobelia. • Family has alternate leaves and milky latex. • Flowers are 5 merous and inferior ovaried. **Campanulaceae - bellflower family The family is divided into two distinct subfamilies - Campanuloideae and Lobelioideae - distinguished by floral symmetry, staminal fusion, and carpel number. They were often considered as separate families. Campanulastrum - bellflower Lobelia - lobelia Subfamily Campanuloideae Subfamily Lobelioideae **Campanulaceae - bellflower family Subfamily Campanuloideae __ CA (5) CO (5) A 5 G (3-5) Campanula and relatives have actinomorphic flowers, stamens not fused, and 3-5 fused carpels. Note the 3 styles of Campanula to the left. **Campanulaceae - bellflower family Triodanis perfoliata - Venus looking glass Secondary pollen presentation **Campanulaceae - bellflower family Campanulastrum americana - tall bellflower **Campanulaceae - bellflower family Campanula rotundifolia Campanula rapunculoides Bluebell - circumboreal European bellflower **Campanulaceae - bellflower family Subfamily Lobelioideae Lobelia and relatives have __ zygomorphic flowers, stamens fused CA (5) CO (5) A (5) G (2) into a tube in which the pollen is shed, and 2 fused carpels. Style pushes pollen out through the tube. Style Staminal tube **Campanulaceae -
A Translation of the Linnaean Dissertation the Invisible World
BJHS 49(3): 353–382, September 2016. © British Society for the History of Science 2016 doi:10.1017/S0007087416000637 A translation of the Linnaean dissertation The Invisible World JANIS ANTONOVICS* AND JACOBUS KRITZINGER** Abstract. This study presents the first translation from Latin to English of the Linnaean disser- tation Mundus invisibilis or The Invisible World, submitted by Johannes Roos in 1769. The dissertation highlights Linnaeus’s conviction that infectious diseases could be transmitted by living organisms, too small to be seen. Biographies of Linnaeus often fail to mention that Linnaeus was correct in ascribing the cause of diseases such as measles, smallpox and syphilis to living organisms. The dissertation itself reviews the work of many microscopists, especially on zoophytes and insects, marvelling at the many unexpected discoveries. It then discusses and quotes at length the observations of Münchhausen suggesting that spores from fungi causing plant diseases germinate to produce animalcules, an observation that Linnaeus claimed to have confirmed. The dissertation then draws parallels between these findings and the conta- giousness of many human diseases, and urges further studies of this ‘invisible world’ since, as Roos avers, microscopic organisms may cause more destruction than occurs in all wars. Introduction Here we present the first translation from Latin to English of the Linnaean dissertation published in 1767 by Johannes Roos (1745–1828) entitled Dissertatio academica mundum invisibilem, breviter delineatura and republished by Carl Linnaeus (1707– 1778) several years later in the Amoenitates academicae under the title Mundus invisibi- lis or The Invisible World.1 Roos was a student of Linnaeus, and the dissertation is important in highlighting Linnaeus’s conviction that infectious diseases could be trans- mitted by living organisms. -
Uribe-Convers Et Al. 2017
Molecular Phylogenetics and Evolution 107 (2017) 551–563 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Phylogenetic relationships of Burmeistera (Campanulaceae: Lobelioideae): Combining whole plastome with targeted loci data in a recent radiation ⇑ Simon Uribe-Convers a, , Monica M. Carlsen a,1, Laura P. Lagomarsino a,b, Nathan Muchhala a a University of Missouri-St. Louis, Biology Department, One University Blvd., Research Building, St. Louis, MO 63121, USA b University of Gothenburg, Department of Biological and Environmental Sciences, Carl Skottsbergs gata 22B, P.O. Box 461, SE 405 30 Göteborg, Sweden article info abstract Article history: The field of molecular systematics has benefited greatly with the advent of high-throughput sequencing Received 23 September 2016 (HTS), making large genomic datasets commonplace. However, a large number of targeted Sanger Revised 6 December 2016 sequences produced by many studies over the last two decades are publicly available and should not Accepted 9 December 2016 be overlooked. In this study, we elucidate the phylogenetic relationships of the plant genus Available online 21 December 2016 Burmeistera (Campanulaceae: Lobelioideae), while investigating how to best combine targeted Sanger loci with HTS data. We sequence, annotate, and analyze complete to nearly complete plastomes for a subset Keywords: of the genus. We then combine these data with a much larger taxonomic dataset for which only Sanger Andes sequences are available, making this the most comprehensively sampled study in the genus to date. We Bellflowers Character evolution show that using a phylogeny inferred from the species with plastome data as a topological constraint for Genome skimming the larger dataset increases the resolution of our data and produces a more robust evolutionary hypoth- Plastome esis for the group. -
The Campanulaceae of Ohio1
CORE Metadata, citation and similar papers at core.ac.uk Provided by KnowledgeBank at OSU 142 WIENS ET AL. Vol. 62 THE CAMPANULACEAE OF OHIO1 ROBERT W. CRUDEN2 Department of Botany and Plant Pathology, Ohio State University, Columbus 10 In Ohio the family Campanulaceae is represented by three genera: Campanula, Lobelia, and Specularia; and eleven species, of which five are common throughout the state and two are quite limited in their distribution. Following the key to species each species is briefly described, and distribution, common names, chromosome numbers, if known, and other pertinent data are given. Chromosome numbers are those given in Darlington and Wylie (1956) and in the papers of Bowden (1959a, 1959b). Average time of flowering is indi- ^ontribution Nc. 666 of the Department of Botany and Plant Pathology, The Ohio State University. Research completed while a National Science Foundation Co-operative Fellow. 2Present address: Department of Botany, University of California, Berkeley 4, California. THE OHIO JOURNAL OF SCIENCE 62(3): 142, May, 1962. No. 3 CAMPANULACEAE OF OHIO 143 cated as well as the extreme flowering dates as determined from a study of her- barium material. The genera and species are arranged alphabetically. Distri- bution maps are included. A dot represents a collection of a particular species in a given county. No attempt has been made to indicate the general area of collection within the county, as a majority of herbarium specimens do not have this information. It should also be pointed out that many of the collections examined are forty or more years old and thus the distribution maps do not neces- sarily indicate present distribution. -
Wildflower in Focus: Cardinal Flower
throated hummingbirds. Their vivid color is the traditional color of the robes worn by Roman Wildflower in Focus Catholic Cardinals - and thus the name. Their hue is also similar to the color of the native male bird Text by Melanie Choukas-Bradley that shares the name cardinal. Growing in wet Artwork by Tina Thieme Brown meadows, springs, freshwater marshes, and along streams, rivers, and ponds throughout the state, the Cardinal Flower cardinal flower is one of several members of the Lobelia cardinalis L. Lobelia genus native to Maryland and the only one Bellflower or Bluebell Family (Campanulaceae) with red flowers. Other Lobelias growing here [Some taxonomists place this genus in a separate have flowers ranging from blue to whitish-blue, family — the Lobelia Family (Lobeliaceae)] lilac, and rarely white. The cardinal flower blooms during the verdant days of mid to late summer and stays in bloom as autumn stirs. Specific Characteristics of the Cardinal Flower Flowers: Scarlet, irregular, 2-lipped, with a 2-lobed upper lip, a 3-lobed lower one and a tubular base. Sexual parts protrude in a beak-like fashion (see illustration). Flowers 1-2" long and wide in upright racemes. Five sepals are thin (almost hair-like). Leaves: Alternate, simple, lanceolate to oblong or narrowly ovate, tapered to apex and base, pubescent or glabrous. Toothed, often irregularly so (sometimes dentate). Short-petioled to sessile, 2-7" long. Height and Growth Habit: 1-5'; usually unbranched. Range: New Brunswick to Minnesota, south to the Gulf of Mexico. Herbal Lore: American Indians used the roots and leaves of this plant for a number of conditions, including syphilis, typhoid, fevers, headaches and rheumatism. -
Phylogeny and Phylogenetic Nomenclature of the Campanulidae Based on an Expanded Sample of Genes and Taxa
Systematic Botany (2010), 35(2): pp. 425–441 © Copyright 2010 by the American Society of Plant Taxonomists Phylogeny and Phylogenetic Nomenclature of the Campanulidae based on an Expanded Sample of Genes and Taxa David C. Tank 1,2,3 and Michael J. Donoghue 1 1 Peabody Museum of Natural History & Department of Ecology & Evolutionary Biology, Yale University, P. O. Box 208106, New Haven, Connecticut 06520 U. S. A. 2 Department of Forest Resources & Stillinger Herbarium, College of Natural Resources, University of Idaho, P. O. Box 441133, Moscow, Idaho 83844-1133 U. S. A. 3 Author for correspondence ( [email protected] ) Communicating Editor: Javier Francisco-Ortega Abstract— Previous attempts to resolve relationships among the primary lineages of Campanulidae (e.g. Apiales, Asterales, Dipsacales) have mostly been unconvincing, and the placement of a number of smaller groups (e.g. Bruniaceae, Columelliaceae, Escalloniaceae) remains uncertain. Here we build on a recent analysis of an incomplete data set that was assembled from the literature for a set of 50 campanulid taxa. To this data set we first added newly generated DNA sequence data for the same set of genes and taxa. Second, we sequenced three additional cpDNA coding regions (ca. 8,000 bp) for the same set of 50 campanulid taxa. Finally, we assembled the most comprehensive sample of cam- panulid diversity to date, including ca. 17,000 bp of cpDNA for 122 campanulid taxa and five outgroups. Simply filling in missing data in the 50-taxon data set (rendering it 94% complete) resulted in a topology that was similar to earlier studies, but with little additional resolution or confidence.