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Aliso: A Journal of Systematic and Evolutionary Botany Volume 32 | Issue 2 Article 3 2015 Index Volume 32 Follow this and additional works at: http://scholarship.claremont.edu/aliso Recommended Citation (2015) "Index Volume 32," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 32: Iss. 2, Article 3. Available at: http://scholarship.claremont.edu/aliso/vol32/iss2/3 Aliso, 32(2), p. 89 ISSN 0065-6275 (print), 2327-2929 (online) INDEX TO VOLUME 32, ALISO Includes authors, titles, taxa, and salient concepts appearing in the scientific papers, as well as additional terms of use in information retrieval. New taxa and combinations appear in boldface. Page numbers reflect the location where an indexing term appears or—if it occurs repeatedly—receives special mention. Acanthaceae 1–5, 7, 12–13, 15, 17, 22, Keys 1, 18–19, 35, 63, 65, 70–71, 78, 83 Photosynthesis genes 51 28, 32, 34–36 Leaves 3–5 Phylogenetics 1–5, 7, 12, 17–18, 22, 27, Alternate start codons 47, 49–53 Lectotype 55–57, 59–60, 70–71, 77 34–36 Anisosepalum (revision) 19–21 Leptosiphon chrysanthus 55, 58–60 Plastid genome 47–53 Arizona 60, 63–65, 67, 78–79, 81, 83, 86 Leptosiphon chrysanthus subsp. decorus Pollen 7–11, 43–44 Asparagales 47–53 55, 59–60 Porter, J. M., Patterson, R. W.—A Baja California 55, 67, 70, 75, 78 Liebre Mountains 67, 70 fistful of Polemoniaceae: new British Columbia, Canada 75, 78 Linanthus bigelovii subsp. johnsonii 55, names and combinations 55– Canada 75, 78 60–61, 63–64 88 Chloroplast genome 47–53 Linanthus californicus subsp. glandulosus Principal components analysis 83–84 Chromosome numbers 17, 45 55, 71 RNA editing 52 Colorado 75, 77–79 Linanthus californicus subsp. tomentosus Rocky Mountains 75, 78 Colorado desert 60, 63–64, 70, 75 55, 71 Saintpauliopsis (revision) 28–31 Daniel, T. F., McDade, L. A.—Nelso- Linanthus dichotomus subsp. pattersonii San Bernardino Mountains 60, 64, nioideae (Lamiales: Acantha- 55, 67–70 San Gabriel Mountains 63–64, 70–71 ceae): revision of genera and Linanthus maculatus subsp. emaculatus San Jacinto Mountains 71, 77 catalog of species 1–45 55, 71–75 Santa Ana Mountains 71 Dayia glutinosa 55–56 Linanthus maricopensis 55, 64–67 Santa Monica Mountains 71 Dayia havardii 55–56 Linanthus pungens subsp. hallii 55, 75–78 Seeds 12–17 Dayia sonorae 55–56 Linanthus pungens subsp. hookeri 55, 75– Sierra Madre Occidental 83 Distribution map 21, 24, 27, 30, 34 78 Sierra Nevada 64 Dunes 71, 75 Linanthus pungens subsp. pulchriflorus Sonoran desert 55, 63–64, 67, 70 Elytraria (revision) 21–25 55, 75–78 Staurogyne (revision) 31–41 Flowers 5–7 Linanthus watsonii subsp. dolomiticus 55, Staurogyne guianensis 37 Fourier analysis 83–84 81, 83 Staurogyne macrobotrya 8 Frame shift 50 Linanthus watsonii subsp. laccolithicus Texas 56, 60, 63 Gene duplication 49–52 55, 79–81, 83 Transverse Ranges 64, 70–71 Gene loss 47, 50–53 Loeselia glandulosa subsp. sonorae 55, Trichomes 60–61, 63–65, 70–71 Gene map 48 83–85 trnL-trnF region 55, 57 Gene reversal 51 Maricopa Mountains 64–65, 67 Turkey 47–49 Genome size 49–50 McDade, L. A. 1–45 Utah 64, 77–79 Giliastrum stewartii 55–57 Mexico 55–57, 67, 70, 75, 83, 86 Vespertine (nocturnal) flowering 61, 65, Great Basin 75, 78 Mojave desert 60, 63–64, 70, 78 68, 75 Habit 1, 3, 5 Monocotyledons 47–50, 53 Washington 75, 77–78 Hygroscopic trichomes 12–17, 44–45 Montana 78–79 Wilson, C. A.—The complete plastid Idaho 78 Nelsonia (revision) 25–28 genome sequence of Iris gate- Indels 50–52 Nelsonioideae (revision) 18–41 sii (section Oncocyclus), Iridaceae 47, 49 Nevada 63–64, 67, 70, 77–78, 81 a bearded species from south- Isolectotype 57, 59, 77 Oregon 75, 77–78 eastern Turkey 47–54 ITS region 55, 57 Patterson, R. W. 55–88 Wyoming 77–79.

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THAI FOREST BULL., BOT. 47(2): 241–259. 2019. DOI https://doi.org/10.20531/tfb.2019.47.2.14 A checklist of Acanthaceae subfamily Nelsonioideae in Thailand THIAMHATHAI CHOOPAN1,*, PAUL J. GROTE2, KONGKANDA CHAYAMARIT3 & DAVID A. SIMPSON4 ABSTRACT A checklist of Acanthaceae subfamily Nelsonioideae in Thailand is presented. Two genera (Nelsonia and Staurogyne) and 29 species are considered native to Thailand, including new species Staurogyne kaengkrachanense. Ecological and distributional data, together with a key to the species, are provided. KEYWORDS: Nelsonia, Staurogyne, taxonomy, Thailand. Accepted for publication: 12 November 2019. Published online: 28 November 2019 INTRODUCTION stenophylla Bremek. were listed in the synonymy of Staurogyne setigera (Nees) Kuntze. In the Thai Acanthaceae subfamily Nelsonioideae Plant Names List (Forest Herbarium, 2001), one comprises seven genera and 170 species of herbs species in each of Nelsonia and Staurogyne was and shrubs that occur primarily in tropical regions recorded for Thailand. Based on a revised study of of both the Old and New Worlds. In Thailand, Craib this subfamily (Choopan, 2013), the list of taxa in (1912) recorded three genera (Nelsonia R.Br., Nelsonia (1 species), Ophiorrhiziphyllon (1 species), Ophiorrhiziphyllon Kurz and Staurogyne Wall.), and Staurogyne (26 species) has been revised with one species in each. Ridley (1923) recorded two (Pooma & Suddee, 2014), moreover, S. longeciliata genera (Nelsonia and Staurogyne) and 29 species in has been reinstated according to the traits distinguish the Malay Peninsula. Benoist (1935) studied the from S. lanceolata (Choopan, 2013). However, the taxonomy of Acanthaceae in the Indo-Chinese region, genus Ophiorrhiziphyllon has now been reduced to primarily based on characters of the sepals, corolla a synonym of Staurogyne based on phylogenetic lobes, number of stamens, shape of the corolla tube data (Daniel & McDade, 2014).
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Staurogyne Nitida, a New Combination Among Brazilian Acanthaceae
Phytotaxa 374 (1): 097–098 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2018 Magnolia Press Correspondence ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.374.1.10 Staurogyne nitida, a new combination among Brazilian Acanthaceae DENISE MONTE BRAZ1* & THOMAS F. DANIEL2 1Departamento de Botânica, Instituto de Ciências Biológicas e da Saúde, Universidade Federal Rural do Rio de Janeiro, BR 465, Km 7, Caixa Postal 74541, 23890-000, Seropédica, Rio de Janeiro, Brazil. 2 Department of Botany, California Academy of Sciences, 55 Music Concourse Drive, Golden Gate Park, San Francisco, California 94118. * Author for correspondence; E-mail: [email protected]; [email protected] Staurogyne carvalhoi is a later heterotypic synonym of Ebermaiera nitida. The new combination Staurogyne nitida, based on the older name, is herewith proposed. Staurogyne carvalhoi é um sinônimo heterotípico posterior de Ebermaiera nitida. A nova combinação, Staurogyne nitida, é aqui proposta com base no nome anterior. Keywords: Nelsonioideae, Staurogyne carvalhoi, synonym, nomenclature Introduction Staurogyne Wallich (1831: 80) (Nelsonioideae, Acanthaceae) comprises 145 species distributed in Asia, Africa and the Americas (Champluvier 1991, Daniel & McDade 2014). In the Neotropics the genus is represented by 28 species (Braz & Monteiro 2017), most of which have been described in the genus Ebermaiera Nees von Esenbeck (1832: 75), which was treated as a synonym of Staurogyne by Kuntze (1891). Staurogyne carvalhoi Profice (2000: 203) was described based on specimens collected in the Brazilian states of Bahia and Espírito Santo. While examining historical collections of Acanthaceae from Brazil, we discovered that the type of Ebermaiera nitida Moore (1879: 812) (Fig.
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Acanthaceae Nelsonioideae Acanthoideae (Pseuderanthemum) (SYSTEMATIC STUDY of ACANTHACEAE, SUBFAMILIES NELSONIOIDEAE and A
เทียมหทัย ชูพันธ์ : การศึกษาด้านอนุกรมวิธานของพรรณพืชวงศ์ Acanthaceae วงศ์ยอย่ Nelsonioideae และ Acanthoideae ( Pseuderanthemum ) ในประเทศไทย (SYSTEMATIC STUDY OF ACANTHACEAE, SUBFAMILIES NELSONIOIDEAE AND ACANTHOIDEAE ( PSEUDERANTHEMUM ), IN THAILAND) อาจารย์ทีFปรึกษา : ดร.พอล เจ โกรดิ, 479 หน้า. การศึกษาด้านอนุกรมวิธานของพรรณพืชวงศ์ Acanthaceae วงศ์ยอย่ Nelsonioideae และ Acanthoideae ( Pseuderanthemum ) ในประเทศไทย พบตัวอยางพืชทั่ NงสิNน 4 สกุล 45 แทกซา ในจํานวนนีNเป็นพืชถิFนเดียวของประเทศ 16 แทกซา โดยพบวาเป็นพืชทีFมีการรายงานเป็นครั่ Nงแรก และคาดวาจะเป็นพืชชนิดใหม่ ของโลก่ 3 แทกซา เป็นพืชปลูกเพืFอเป็นไม้ประดับ 4 แทกซา คือ Pseuderanthemum carruthersii P. laxiflorum P. metallicum P. reticulatum เพืFอเป็นสมุนไพร 1 แทกซา คือ P. “palatiferum ” นอกจากนีNได้จัดทํารูปวิธานระดับสกุล ระดับชนิด และแทกซา ให้ คําบรรยายลักษณะทางพฤกษศาสตร์ ภาพถ่ายและภาพวาด ระบุตัวอยางต้นแบบ่ ตัวอยางศึกษาและ่ เอกสารอ้างอิงตามหลักอนุกรมวิธาน พืชมีการกระจายพันธุ์อยูทั่ วประเทศในนิเวศของป่าหลายแบบF บางชนิดมีการกระจายพันธุ์กว้างและบางชนิดพบเฉพาะพืNนทีF ศึกษาลักษณะของปากใบ เซลล์เยืFอบุผิวใบ ซิสโทลิตท์ และรูปแบบการเรียงตัวของเส้นใบ พบวา่ ลักษณะทางกายวิภาคบางประการสามารถนํามาใช้จําแนกพืชในระดับสกุลได้ แตเป็นได้่ เพียงข้อมูลพืNนฐานของพืชแตละชนิด่ ศึกษาลักษณะเรณูของพืชด้วยกล้องจุลทรรศน์แบบใช้แสง และกล้องจุลทรรศน์อิเล็กตรอนแบบส่องกราด พบวา่ ลักษณะสัณฐานวิทยาของเรณูพืชสามารถ นํามาใช้จําแนกพืชในระดับสกุลและระดับทีFตํFากวาสกุลได้่ การวิเคราะห์สายสัมพันธ์ทางวิวัฒนาการของพืช จากลําดับนิวคลีโอไทด์ในไรโบโซมดี เอ็นเอ internal transcribed spacer (ITS) และคลอโรพลาสต์ดีเอ็นเอชนิด trnL-F
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Agneta Julia Borg
Evolutionary relationships in Thunbergioideae and other early branching lineages of Acanthac e a e Agneta Julia Borg Evolutionary relationships in Thunbergioideae and other early branching lineages of Acanthaceae Agneta Julia Borg ©Agneta Julia Borg, Stockholm 2012 Cover illustration: From top left, Mendoncia retusa, Thunbergia convolvulifolia , Pseudocalyx saccatus, Crossandra strobilifera, Avicennia bicolor, Elytraria marginata. Photos: Agneta Julia Borg and Jürg Schönenberger. ISBN 978-91-7447-445-9 Printed in Sweden by Universitetsservice US-AB, Stockholm 2012 Distributor: Department of Botany, Stockholm University Academic dissertation for the degree of Doctor of Philosophy in Plant Sys- tematics presented at Stockholm University 2012 Abstract Borg, A.J. 2012. Evolutionary relationships in Thunbergioideae and other early branching lineages of Acanthaceae. Acanthaceae as circumscribed today consists of the three subfamilies Acan- thoideae (Acanthaceae sensu stricto), Thunbergioideae and Nelsonioideae, plus the genus Avicennia. Due to the morphological dissimilarities of Thun- bergioideae and Nelsonioideae, the delimitation of the family has been con- troversial. The mangrove genus Avicennia was only recently associated with Acanthaceae for the first time, based on molecular evidence, but without morphological support. In this thesis, phylogenetic analyses of nuclear and chloroplast DNA sequences were used to test the monophyly and exact posi- tions of Thunbergioideae and Nelsonioideae, and to infer detailed phyloge- netic relationships within these subfamilies and among major lineages of Acanthaceae. Floral structure and development were comparatively studied in Avicennia and other Acanthaceae using scanning electron microscopy and stereo microscopy. Phylogenetic analyses strongly support monophyly of Thunbergioideae and Nelsonioideae, and place the latter clade with strong support as sister to all other plants treated as Acanthaceae.
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Lamiales – Synoptical Classification Vers
Lamiales – Synoptical classification vers. 2.6.2 (in prog.) Updated: 12 April, 2016 A Synoptical Classification of the Lamiales Version 2.6.2 (This is a working document) Compiled by Richard Olmstead With the help of: D. Albach, P. Beardsley, D. Bedigian, B. Bremer, P. Cantino, J. Chau, J. L. Clark, B. Drew, P. Garnock- Jones, S. Grose (Heydler), R. Harley, H.-D. Ihlenfeldt, B. Li, L. Lohmann, S. Mathews, L. McDade, K. Müller, E. Norman, N. O’Leary, B. Oxelman, J. Reveal, R. Scotland, J. Smith, D. Tank, E. Tripp, S. Wagstaff, E. Wallander, A. Weber, A. Wolfe, A. Wortley, N. Young, M. Zjhra, and many others [estimated 25 families, 1041 genera, and ca. 21,878 species in Lamiales] The goal of this project is to produce a working infraordinal classification of the Lamiales to genus with information on distribution and species richness. All recognized taxa will be clades; adherence to Linnaean ranks is optional. Synonymy is very incomplete (comprehensive synonymy is not a goal of the project, but could be incorporated). Although I anticipate producing a publishable version of this classification at a future date, my near- term goal is to produce a web-accessible version, which will be available to the public and which will be updated regularly through input from systematists familiar with taxa within the Lamiales. For further information on the project and to provide information for future versions, please contact R. Olmstead via email at [email protected], or by regular mail at: Department of Biology, Box 355325, University of Washington, Seattle WA 98195, USA.
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And Phylogenetic Significance Long Been Recognised (Bachmann, 1886
BLUMEA 24 (1978) 101-117 Epidermalhairs of Acanthaceae Khwaja+J. Ahmad Plant Anatomy Laboratory, National Botanic Gardens, Lucknow-226001, India. Summary two belonging to Structure and distribution of the foliar epidermal hairs of 109 species and varieties 39 hairs have Acanthaceae have been studied. Both and non-glandularepidermal genera ofthe family glandular hairs The sub- been recorded in the investigated taxa. The glandular may be subsessile or long-stalked. Glandular head of Glandular head 2-celled, and ii) sessile glandular hairs are two types: i) panduriform, —8- more-celled. Subfamilies Nelsonioideae and Thunbergioideae are character- globular or disc-shaped, 2 or hairs i«*H hv thfi nanduriform hairs, while Mendoncioideae and Acanthoideae have glandular with a globular also only in nine species. Non-glandular hairs are widely head. Long-stalked glandular hairs are present or multicellular are in all but ten They be unicellular, distributed in the family; they present species. may the hairs are of at species uniseriate; rarely they are branched. Though non-glandular diagnosticimportance The like Barleria, and Äphelandra, are quite characteristic. present level only, in some genera Ruttya,, they delimitation of the family Acanthaceae, involving the transfer study does not support Bremekamp's (1965) and the of his subfamilies Thunber- Nelsonioideae to raising of Lindau's (1895) subfamily Scrophulariaceae, rank of families. the retention of Nelsonioideae, gioideae and Mendoncioideae to the independent Instead, Acanthaceae is favoured. Thunbergioideae, Mendoncioideae, and Acanthoideae within the family Introduction The taxonomic and phylogenetic significance of trichomes has long been recognised number ofworkers Solereder, 2 Cowan, by a (Bachmann, 1886; 1908; Cooper, 193 ! 195°! According to Carlquist Metcalfe & Chalk, 1950; Goodspeed, 1954; and Sporne, 1956).
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A Survey of Tricolpate (Eudicot) Phylogenetic Relationships1
American Journal of Botany 91(10): 1627±1644. 2004. A SURVEY OF TRICOLPATE (EUDICOT) PHYLOGENETIC RELATIONSHIPS1 WALTER S. JUDD2,4 AND RICHARD G. OLMSTEAD3 2Department of Botany, University of Florida, Gainesville, Florida 32611 USA; and 3Department of Biology, University of Washington, Seattle, Washington 98195 USA The phylogenetic structure of the tricolpate clade (or eudicots) is presented through a survey of their major subclades, each of which is brie¯y characterized. The tricolpate clade was ®rst recognized in 1989 and has received extensive phylogenetic study. Its major subclades, recognized at ordinal and familial ranks, are now apparent. Ordinal and many other suprafamilial clades are brie¯y diag- nosed, i.e., the putative phenotypic synapomorphies for each major clade of tricolpates are listed, and the support for the monophyly of each clade is assessed, mainly through citation of the pertinent molecular phylogenetic literature. The classi®cation of the Angiosperm Phylogeny Group (APG II) expresses the current state of our knowledge of phylogenetic relationships among tricolpates, and many of the major tricolpate clades can be diagnosed morphologically. Key words: angiosperms; eudicots; tricolpates. Angiosperms traditionally have been divided into two pri- 1992a; Chase et al., 1993; Doyle et al., 1994; Soltis et al., mary groups based on the presence of a single cotyledon 1997, 2000, 2003; KaÈllersjoÈ et al., 1998; Nandi et al., 1998; (monocotyledons, monocots) or two cotyledons (dicotyledons, Hoot et al., 1999; Savolainen et al., 2000a, b; Hilu et al., 2003; dicots). A series of additional diagnostic traits made this di- Zanis et al., 2003; Kim et al., 2004). This clade was ®rst called vision useful and has accounted for the long recognition of the tricolpates (Donoghue and Doyle, 1989), but the name these groups in ¯owering plant classi®cations.
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1 Updates Required to Plant Systematics: A
Updates Required to Plant Systematics: A Phylogenetic Approach, Third Edition, as a Result of Recent Publications (Updated June 13, 2014) As necessitated by recent publications, updates to the Third Edition of our textbook will be provided in this document. It is hoped that this list will facilitate the efficient incorporation new systematic information into systematic courses in which our textbook is used. Plant systematics is a dynamic field, and new information on phylogenetic relationships is constantly being published. Thus, it is not surprising that even introductory texts require constant modification in order to stay current. The updates are organized by chapter and page number. Some require only minor changes, as indicated below, while others will require more extensive modifications of the wording in the text or figures, and in such cases we have presented here only a summary of the major points. The eventual fourth edition will, of course, contain many organizational changes not treated below. Page iv: Meriania hernandii Meriania hernandoi Chapter 1. Page 12, in Literature Cited, replace “Stuessy, T. F. 1990” with “Stuessy, T. F. 2009,” which is the second edition of this book. Stuessy, T. F. 2009. Plant taxonomy: The systematic evaluation of comparative data. 2nd ed. Columbia University Press, New York. Chapter 2. Page 37, column 1, line 5: Stuessy 1983, 1990;… Stuessy 1983, 2009; … And in Literature Cited, replace “Stuessy 1990” with: Stuessy, T. F. 2009. Plant taxonomy: The systematic evaluation of comparative data. 2nd ed. Columbia University Press, New York. Chapter 4. Page 58, column 1, line 5: and Dilcher 1974). …, Dilcher 1974, and Ellis et al.
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The Leipzig Catalogue of Plants (LCVP) ‐ an Improved Taxonomic Reference List for All Known Vascular Plants
Freiberg et al: The Leipzig Catalogue of Plants (LCVP) ‐ An improved taxonomic reference list for all known vascular plants Supplementary file 3: Literature used to compile LCVP ordered by plant families 1 Acanthaceae AROLLA, RAJENDER GOUD; CHERUKUPALLI, NEERAJA; KHAREEDU, VENKATESWARA RAO; VUDEM, DASHAVANTHA REDDY (2015): DNA barcoding and haplotyping in different Species of Andrographis. In: Biochemical Systematics and Ecology 62, p. 91–97. DOI: 10.1016/j.bse.2015.08.001. BORG, AGNETA JULIA; MCDADE, LUCINDA A.; SCHÖNENBERGER, JÜRGEN (2008): Molecular Phylogenetics and morphological Evolution of Thunbergioideae (Acanthaceae). In: Taxon 57 (3), p. 811–822. DOI: 10.1002/tax.573012. CARINE, MARK A.; SCOTLAND, ROBERT W. (2002): Classification of Strobilanthinae (Acanthaceae): Trying to Classify the Unclassifiable? In: Taxon 51 (2), p. 259–279. DOI: 10.2307/1554926. CÔRTES, ANA LUIZA A.; DANIEL, THOMAS F.; RAPINI, ALESSANDRO (2016): Taxonomic Revision of the Genus Schaueria (Acanthaceae). In: Plant Systematics and Evolution 302 (7), p. 819–851. DOI: 10.1007/s00606-016-1301-y. CÔRTES, ANA LUIZA A.; RAPINI, ALESSANDRO; DANIEL, THOMAS F. (2015): The Tetramerium Lineage (Acanthaceae: Justicieae) does not support the Pleistocene Arc Hypothesis for South American seasonally dry Forests. In: American Journal of Botany 102 (6), p. 992–1007. DOI: 10.3732/ajb.1400558. DANIEL, THOMAS F.; MCDADE, LUCINDA A. (2014): Nelsonioideae (Lamiales: Acanthaceae): Revision of Genera and Catalog of Species. In: Aliso 32 (1), p. 1–45. DOI: 10.5642/aliso.20143201.02. EZCURRA, CECILIA (2002): El Género Justicia (Acanthaceae) en Sudamérica Austral. In: Annals of the Missouri Botanical Garden 89, p. 225–280. FISHER, AMANDA E.; MCDADE, LUCINDA A.; KIEL, CARRIE A.; KHOSHRAVESH, ROXANNE; JOHNSON, MELISSA A.; STATA, MATT ET AL.
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Phylogeny of Lamiidae Reveals Increased Resolution and Support for Internal Relationships That Have Remained Elusive
American Journal of Botany 101(2): 287–299. 2014. P HYLOGENY OF LAMIIDAE 1 N ANCY F . R EFULIO-RODRIGUEZ 2 AND R ICHARD G. OLMSTEAD 2,3 2 Department of Biology, Box 355325, University of Washington, Seattle, Washington 98195 USA • Premise of the study: The Lamiidae, a clade composed of approximately 15% of all fl owering plants, consists of fi ve orders: Boraginales, Gentianales, Garryales, Lamiales, and Solanales; and four families unplaced in an order: Icacinaceae, Metteniusi- aceae, Oncothecaceae, and Vahliaceae. Our understanding of the phylogenetic relationships of Lamiidae has improved signifi - cantly in recent years, however, relationships among the orders and unplaced families of the clade remain partly unresolved. Here, we present a phylogenetic analysis of the Lamiidae based on an expanded sampling, including all families together, for the fi rst time, in a single phylogenetic analyses. • Methods: Phylogenetic analyses were conducted using maximum parsimony, maximum likelihood, and Bayesian approaches. Analyses included nine plastid regions ( atpB , matK , ndhF , psbBTNH , rbcL , rps4 , rps16 , trnL - F , and trnV - atpE ) and the mitochondrial rps3 region, and 129 samples representing all orders and unplaced families of Lamiidae. • Key results: Maximum Likelihood (ML) and Bayesian trees provide good support for Boraginales sister to Lamiales, with successive outgroups (Solanales + Vahlia) and Gentianales, together comprising the core Lamiidae. Early branching patterns are less well supported, with Garryales only poorly supported as sister to the above ‘core’ and a weakly supported clade composed of Icacinaceae, Metteniusaceae, and Oncothecaceae sister to all other Lamiidae. • Conclusions: Our phylogeny of Lamiidae reveals increased resolution and support for internal relationships that have remained elusive.
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(Lamiales: Acanthaceae): Revision of Genera and Catalog of Species Thomas F
Aliso: A Journal of Systematic and Evolutionary Botany Volume 32 | Issue 1 Article 2 2014 Nelsonioideae (Lamiales: Acanthaceae): Revision of Genera and Catalog of Species Thomas F. Daniel Department of Botany, California Academy of Sciences, San Francisco Lucinda A. McDade Rancho Santa Ana Botanic Garden, Claremont, California Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons, and the Ecology and Evolutionary Biology Commons Recommended Citation Daniel, Thomas F. and McDade, Lucinda A. (2014) "Nelsonioideae (Lamiales: Acanthaceae): Revision of Genera and Catalog of Species," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 32: Iss. 1, Article 2. Available at: http://scholarship.claremont.edu/aliso/vol32/iss1/2 Aliso, 32(1), pp. 1–45 ISSN 0065-6275 (print), 2327-2929 (online) NELSONIOIDEAE (LAMIALES: ACANTHACEAE): REVISION OF GENERA AND CATALOG OF SPECIES THOMAS F. DANIEL1,3 AND LUCINDA A. MCDADE2 1Department of Botany, California Academy of Sciences, 55 Music Concourse Drive, Golden Gate Park, San Francisco, California 94118; 2Rancho Santa Ana Botanic Garden, 1500 N. College Avenue, Claremont, California 91711 3Corresponding author ([email protected]) ABSTRACT A taxonomic account of Acanthaceae subfamily Nelsonioideae based on morphological and phylogenetic data treats five genera with 172 species: Anisosepalum (3), Elytraria (21), Nelsonia (2), Saintpauliopsis (1), and Staurogyne (145). Two other currently recognized genera, Gynocraterium and Ophiorrhiziphyllon, are included within Staurogyne, and the new combinations, Staurogyne guianensis and S. macrobotrya, are proposed. Probable apomorphic and other diagnostic macro- and micromorphological characters are discussed relative to the subfamily and genera. Characters of the inflorescence, androecium (especially pollen), and seed show important phylogenetic and diagnostic signal.
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Taxonomic Revision of Staurogyne (Nelsonioideae, Acanthaceae) in the Neotropics
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