Fossil Early Psilophytian & Lycopodian, Spenopsida Lines of Evolution
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Tansley Review Evolution of Development of Vascular Cambia and Secondary Growth
New Phytologist Review Tansley review Evolution of development of vascular cambia and secondary growth Author for correspondence: Rachel Spicer1 and Andrew Groover2 Andrew Groover 1The Rowland Institute at Harvard, Cambridge, MA, USA; 2Institute of Forest Genetics, Pacific Tel: +1 530 759 1738 Email: [email protected] Southwest Research Station, USDA Forest Service, Davis, CA, USA Received: 29 December 2009 Accepted: 14 February 2010 Contents Summary 577 V. Evolution of development approaches for the study 587 of secondary vascular growth I. Introduction 577 VI. Conclusions 589 II. Generalized function of vascular cambia and their 578 developmental and evolutionary origins Acknowledgements 589 III. Variation in secondary vascular growth in angiosperms 581 References 589 IV. Genes and mechanisms regulating secondary vascular 584 growth and their evolutionary origins Summary New Phytologist (2010) 186: 577–592 Secondary growth from vascular cambia results in radial, woody growth of stems. doi: 10.1111/j.1469-8137.2010.03236.x The innovation of secondary vascular development during plant evolution allowed the production of novel plant forms ranging from massive forest trees to flexible, Key words: forest trees, genomics, Populus, woody lianas. We present examples of the extensive phylogenetic variation in sec- wood anatomy, wood formation. ondary vascular growth and discuss current knowledge of genes that regulate the development of vascular cambia and woody tissues. From these foundations, we propose strategies for genomics-based research in the evolution of development, which is a next logical step in the study of secondary growth. I. Introduction this pattern characterizes most extant forest trees, significant variation exists among taxa, ranging from extinct woody Secondary vascular growth provides a means of radially lycopods and horsetails with unifacial cambia (Cichan & thickening and strengthening plant axes initiated during Taylor, 1990; Willis & McElwain, 2002), to angiosperms primary, or apical growth. -
Fern News 67
I " yaASSOCIATION %M@% Of 52% gas. We: (/5sz 67 ”snag; li'iixé‘r' ~ g lSSN 08ll-531l DATE— DECEMBER 1994 ‘30.»? ***************************************t************************** LEADER: Peter Hind, 41 Miller Street, Mount Druitt, 2770 SECRETARY: Moreen Woollett, 3 Currawang Place, Como West, 2226 TREASURER: Joan Moore, 2 Ganne't Street, Gladesville, 2111 SPORE BANK: Dulcie Buddee, 4 Leigh Street, Merrylands, 2160 ****************************************************************** FERNS IN GARDEN DESIGN Some time ago, Diana Snape Leader of the ASGAP Garden Design Group, asked Study Groups to list plants (in our case ferns) that are valuable for garden design. In endeavouring to help Diana, some infomation was gathered together and is recorded here. In the past our Group has paid little attention to questions of design even though several of our Study Group members are obviously interested in the subject and have joined the Garden Design Study Group. It is an important area that needs to be developed and all members are invited to make a contribution to our store of knowledge by advising their thoughts on the subject of ferns in garden design and / or providing comments regarding the suitability or otherwise of particular fern species. Design in gardens like most things is either good or bad depending on personal preference but obviously a well designed garden will be perceived as such by the majority of viewers. To be considered “well designed” gardens probably need to exhibit the following features: — Be of attractive 0r pleasing appearance - Look natural or complementary to the environment - Suit :1 range of out of doors uses - Be relatively easy to maintain. One of the challenges in gardening is to maintain form and appearance of the garden without it being an all time consuming occupation. -
The Fern Family Blechnaceae: Old and New
ANDRÉ LUÍS DE GASPER THE FERN FAMILY BLECHNACEAE: OLD AND NEW GENERA RE-EVALUATED, USING MOLECULAR DATA Tese apresentada ao Programa de Pós-Graduação em Biologia Vegetal do Departamento de Botânica do Instituto de Ciências Biológicas da Universidade Federal de Minas Gerais, como requisito parcial à obtenção do título de Doutor em Biologia Vegetal. Área de Concentração Taxonomia vegetal BELO HORIZONTE – MG 2016 ANDRÉ LUÍS DE GASPER THE FERN FAMILY BLECHNACEAE: OLD AND NEW GENERA RE-EVALUATED, USING MOLECULAR DATA Tese apresentada ao Programa de Pós-Graduação em Biologia Vegetal do Departamento de Botânica do Instituto de Ciências Biológicas da Universidade Federal de Minas Gerais, como requisito parcial à obtenção do título de Doutor em Biologia Vegetal. Área de Concentração Taxonomia Vegetal Orientador: Prof. Dr. Alexandre Salino Universidade Federal de Minas Gerais Coorientador: Prof. Dr. Vinícius Antonio de Oliveira Dittrich Universidade Federal de Juiz de Fora BELO HORIZONTE – MG 2016 Gasper, André Luís. 043 Thefern family blechnaceae : old and new genera re- evaluated, using molecular data [manuscrito] / André Luís Gasper. – 2016. 160 f. : il. ; 29,5 cm. Orientador: Alexandre Salino. Co-orientador: Vinícius Antonio de Oliveira Dittrich. Tese (doutorado) – Universidade Federal de Minas Gerais, Departamento de Botânica. 1. Filogenia - Teses. 2. Samambaia – Teses. 3. RbcL. 4. Rps4. 5. Trnl. 5. TrnF. 6. Biologia vegetal - Teses. I. Salino, Alexandre. II. Dittrich, Vinícius Antônio de Oliveira. III. Universidade Federal de Minas Gerais. Departamento de Botânica. IV. Título. À Sabrina, meus pais e a vida, que não se contém! À Lucia Sevegnani, que não pode ver esta obra concluída, mas que sempre foi motivo de inspiração. -
JUDD W.S. Et. Al. (2002) Plant Systematics: a Phylogenetic Approach. Chapter 7. an Overview of Green
UNCORRECTED PAGE PROOFS An Overview of Green Plant Phylogeny he word plant is commonly used to refer to any auto- trophic eukaryotic organism capable of converting light energy into chemical energy via the process of photosynthe- sis. More specifically, these organisms produce carbohydrates from carbon dioxide and water in the presence of chlorophyll inside of organelles called chloroplasts. Sometimes the term plant is extended to include autotrophic prokaryotic forms, especially the (eu)bacterial lineage known as the cyanobacteria (or blue- green algae). Many traditional botany textbooks even include the fungi, which differ dramatically in being heterotrophic eukaryotic organisms that enzymatically break down living or dead organic material and then absorb the simpler products. Fungi appear to be more closely related to animals, another lineage of heterotrophs characterized by eating other organisms and digesting them inter- nally. In this chapter we first briefly discuss the origin and evolution of several separately evolved plant lineages, both to acquaint you with these important branches of the tree of life and to help put the green plant lineage in broad phylogenetic perspective. We then focus attention on the evolution of green plants, emphasizing sev- eral critical transitions. Specifically, we concentrate on the origins of land plants (embryophytes), of vascular plants (tracheophytes), of 1 UNCORRECTED PAGE PROOFS 2 CHAPTER SEVEN seed plants (spermatophytes), and of flowering plants dons.” In some cases it is possible to abandon such (angiosperms). names entirely, but in others it is tempting to retain Although knowledge of fossil plants is critical to a them, either as common names for certain forms of orga- deep understanding of each of these shifts and some key nization (e.g., the “bryophytic” life cycle), or to refer to a fossils are mentioned, much of our discussion focuses on clade (e.g., applying “gymnosperms” to a hypothesized extant groups. -
Brisbane Native Plants by Suburb
INDEX - BRISBANE SUBURBS SPECIES LIST Acacia Ridge. ...........15 Chelmer ...................14 Hamilton. .................10 Mayne. .................25 Pullenvale............... 22 Toowong ....................46 Albion .......................25 Chermside West .11 Hawthorne................. 7 McDowall. ..............6 Torwood .....................47 Alderley ....................45 Clayfield ..................14 Heathwood.... 34. Meeandah.............. 2 Queensport ............32 Trinder Park ...............32 Algester.................... 15 Coopers Plains........32 Hemmant. .................32 Merthyr .................7 Annerley ...................32 Coorparoo ................3 Hendra. .................10 Middle Park .........19 Rainworth. ..............47 Underwood. ................41 Anstead ....................17 Corinda. ..................14 Herston ....................5 Milton ...................46 Ransome. ................32 Upper Brookfield .......23 Archerfield ...............32 Highgate Hill. ........43 Mitchelton ...........45 Red Hill.................... 43 Upper Mt gravatt. .......15 Ascot. .......................36 Darra .......................33 Hill End ..................45 Moggill. .................20 Richlands ................34 Ashgrove. ................26 Deagon ....................2 Holland Park........... 3 Moorooka. ............32 River Hills................ 19 Virginia ........................31 Aspley ......................31 Doboy ......................2 Morningside. .........3 Robertson ................42 Auchenflower -
Pteridophyte Fungal Associations: Current Knowledge and Future Perspectives
This is a repository copy of Pteridophyte fungal associations: Current knowledge and future perspectives. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/109975/ Version: Accepted Version Article: Pressel, S, Bidartondo, MI, Field, KJ orcid.org/0000-0002-5196-2360 et al. (2 more authors) (2016) Pteridophyte fungal associations: Current knowledge and future perspectives. Journal of Systematics and Evolution, 54 (6). pp. 666-678. ISSN 1674-4918 https://doi.org/10.1111/jse.12227 © 2016 Institute of Botany, Chinese Academy of Sciences. This is the peer reviewed version of the following article: Pressel, S., Bidartondo, M. I., Field, K. J., Rimington, W. R. and Duckett, J. G. (2016), Pteridophyte fungal associations: Current knowledge and future perspectives. Jnl of Sytematics Evolution, 54: 666–678., which has been published in final form at https://doi.org/10.1111/jse.12227. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website. -
Flora of New Zealand Ferns and Lycophytes
FLORA OF NEW ZEALAND FERNS AND LYCOPHYTES LOXSOMATACEAE P.J. BROWNSEY & L.R. PERRIE Fascicle 7 – MARCH 2015 © Landcare Research New Zealand Limited 2015. Unless indicated otherwise for specific items, this copyright work is licensed under the Creative Commons Attribution 3.0 New Zealand license. Attribution if redistributing to the public without adaptation: “Source: Landcare Research" Attribution if making an adaptation or derivative work: “Sourced from Landcare Research" See Image Information for copyright and licence details for images. CATALOGUING IN PUBLICATION Brownsey, P.J. (Patrick John), 1948- Flora of New Zealand [electronic resource] : ferns and lycophytes. Fascicle 7, Loxsomataceae / P.J. Brownsey and L.R. Perrie. -- Lincoln, N.Z. : Manaaki Whenua Press, 2015. 1 online resource ISBN 978-0-478-34776-0 (pdf) ISBN 978-0-478-34761-6 (set) 1.Ferns -- New Zealand - Identification. I. Perrie, L.R. (Leon Richard). II. Title. III. Manaaki Whenua- Landcare Research New Zealand Ltd. UDC 582.394.736(931)DC 587.30993 DOI: 10.7931/B1WC7J This work should be cited as: Brownsey, P.J. & Perrie, L.R. 2015: Loxsomataceae. In: Breitwieser, I.; Heenan, P.B.; Wilton, A.D. Flora of New Zealand — Ferns and Lycophytes. Fascicle 7. Manaaki Whenua Press, Lincoln. http://dx.doi.org/10.7931/B1WC7J Cover image: Loxsoma cunninghamii, broadly ovate mature frond. Contents Introduction..............................................................................................................................................1 Taxa Loxsomataceae C.Presl ................................................................................................................... -
Doodia Australis
Doodia australis COMMON NAME Rasp fern SYNONYMS Doodia media subsp. australis Parris; Doodia kunthiana sensu A.Cunn.; Doodia australis (Parris) Parris, Blechnum parrisiae Christenh. FAMILY Blechnaceae AUTHORITY Doodia australis (Parris) Parris FLORA CATEGORY Vascular – Native ENDEMIC TAXON No ENDEMIC GENUS Kerikeri. Photographer: John Barkla No ENDEMIC FAMILY No STRUCTURAL CLASS Ferns NVS CODE DOOAUS CHROMOSOME NUMBER 2n = 128 CURRENT CONSERVATION STATUS 2012 | Not Threatened PREVIOUS CONSERVATION STATUSES 2009 | Not Threatened 2004 | Not Threatened DISTRIBUTION Indigenous. Kermadec Islands (Raoul and Macauley Islands). New Coromandel. Dec 1982. Photographer: Jeremy Zealand: Three Kings, North and South Islands from Te Paki south to Rolfe Wellington, the Marlborough Sounds, north-west Nelson and Banks Peninsula. Abundant north of the Waikato, otherwise scarce. Present in Australia, Norfolk and Lord Howe Islands. HABITAT Coastal to lowland in open or forested sites, within light scrub, in rough pasture, and even known as a weedy fern of urban gardens and environments. FEATURES Vegetative reproduction by stolons or shortly branching rhizome. Rhizome rarely prostrate and creeping; clad in dense black scales. Fertile and sterile fronds mostly similar sometimes moderately dimorphic. Fronds more or less erect or sterile fronds sometimes inclined to prostrate; harsh; lamina 110-600 mm long. Stipes and raches bearing brown scales, these more persistent at the stipe base though mostly shed at frond maturation; pubescent. Lower pinnae attached by costae, sometimes with auricles developed, or very rarely adnate to the rachis, lowest pair rarely longer than the pairs immediately above them; middle pinnae usually completely, but often partly, adnate, occasionally decurrent, rarely auriculate; upper pinnae adnate to decurrent. -
Fern Classification
16 Fern classification ALAN R. SMITH, KATHLEEN M. PRYER, ERIC SCHUETTPELZ, PETRA KORALL, HARALD SCHNEIDER, AND PAUL G. WOLF 16.1 Introduction and historical summary / Over the past 70 years, many fern classifications, nearly all based on morphology, most explicitly or implicitly phylogenetic, have been proposed. The most complete and commonly used classifications, some intended primar• ily as herbarium (filing) schemes, are summarized in Table 16.1, and include: Christensen (1938), Copeland (1947), Holttum (1947, 1949), Nayar (1970), Bierhorst (1971), Crabbe et al. (1975), Pichi Sermolli (1977), Ching (1978), Tryon and Tryon (1982), Kramer (in Kubitzki, 1990), Hennipman (1996), and Stevenson and Loconte (1996). Other classifications or trees implying relationships, some with a regional focus, include Bower (1926), Ching (1940), Dickason (1946), Wagner (1969), Tagawa and Iwatsuki (1972), Holttum (1973), and Mickel (1974). Tryon (1952) and Pichi Sermolli (1973) reviewed and reproduced many of these and still earlier classifica• tions, and Pichi Sermolli (1970, 1981, 1982, 1986) also summarized information on family names of ferns. Smith (1996) provided a summary and discussion of recent classifications. With the advent of cladistic methods and molecular sequencing techniques, there has been an increased interest in classifications reflecting evolutionary relationships. Phylogenetic studies robustly support a basal dichotomy within vascular plants, separating the lycophytes (less than 1 % of extant vascular plants) from the euphyllophytes (Figure 16.l; Raubeson and Jansen, 1992, Kenrick and Crane, 1997; Pryer et al., 2001a, 2004a, 2004b; Qiu et al., 2006). Living euphyl• lophytes, in turn, comprise two major clades: spermatophytes (seed plants), which are in excess of 260 000 species (Thorne, 2002; Scotland and Wortley, Biology and Evolution of Ferns and Lycopliytes, ed. -
Doodia Hindii ( Blechnaceae) a New Species from North Eastern New South Wales, Australia
Telopea 12(2) 257–261 Doodia hindii ( Blechnaceae) a new species from north eastern New South Wales, Australia T. Carrick Chambers National Herbarium of NSW, Mrs Macquaries Road, Sydney, NSW 2000, Australia Email: [email protected] Abstract Doodia hindii Tindale ex T.C.Chambers is described for the first time. This is a rarely collected species from rainforest in mountain regions of north eastern New South Wales, bringing to nine the number of species of Doodia in Australia . Introduction The genus Doodia (Blechnaceae) is estimated to contain more than 30 species distributed through Australasia, Papuasia, Malesia, Sri Lanka and the Pacific region extending north east to Hawaii and as far east as Easter Island (Parris 1972, 1998). Hybrids have been reported among some of the species especially in the D. caudata complex (Andrews 1990). Eight species have been defined by Parris (1998) in the Flora of Australia treatment. By modifying the key provided there, this additional (ninth) Australian taxon can be accommodated as follows (modifications are in italics): 4: Numerous strongly reduced basal pinnae/segments present; abaxial surface of pinnae/segments mid vein either with or without tubercles .............................................................................. 5 5 Rhizome erect, forming caudex up to 30 cm ................................................ 1. D. maxima 5: Rhizome short to long creeping; tubercles present on stipe .......................... 5. D. australis 5a Rhizome short (but may develop an erect -
A Revised Family-Level Classification for Eupolypod II Ferns (Polypodiidae: Polypodiales)
TAXON 61 (3) • June 2012: 515–533 Rothfels & al. • Eupolypod II classification A revised family-level classification for eupolypod II ferns (Polypodiidae: Polypodiales) Carl J. Rothfels,1 Michael A. Sundue,2 Li-Yaung Kuo,3 Anders Larsson,4 Masahiro Kato,5 Eric Schuettpelz6 & Kathleen M. Pryer1 1 Department of Biology, Duke University, Box 90338, Durham, North Carolina 27708, U.S.A. 2 The Pringle Herbarium, Department of Plant Biology, University of Vermont, 27 Colchester Ave., Burlington, Vermont 05405, U.S.A. 3 Institute of Ecology and Evolutionary Biology, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei, 10617, Taiwan 4 Systematic Biology, Evolutionary Biology Centre, Uppsala University, Norbyv. 18D, 752 36, Uppsala, Sweden 5 Department of Botany, National Museum of Nature and Science, Tsukuba 305-0005, Japan 6 Department of Biology and Marine Biology, University of North Carolina Wilmington, 601 South College Road, Wilmington, North Carolina 28403, U.S.A. Carl J. Rothfels and Michael A. Sundue contributed equally to this work. Author for correspondence: Carl J. Rothfels, [email protected] Abstract We present a family-level classification for the eupolypod II clade of leptosporangiate ferns, one of the two major lineages within the Eupolypods, and one of the few parts of the fern tree of life where family-level relationships were not well understood at the time of publication of the 2006 fern classification by Smith & al. Comprising over 2500 species, the composition and particularly the relationships among the major clades of this group have historically been contentious and defied phylogenetic resolution until very recently. Our classification reflects the most current available data, largely derived from published molecular phylogenetic studies. -
Heterospory and Seed Habit Heterospory Is a Phenomenon in Which Two Kinds of Spores Are Borne by the Same Plant
Biology and Diversity of Algae, Bryophyta and Pteridophytes Paper Code: BOT-502 BLOCK – IV: PTERIDOPHYTA Unit –19: Hetrospory and Seed Habit Unit–20: Fossil Pteridophytes By Dr. Prabha Dhondiyal Department of Botany Uttarakhand Open University Haldwani E-mail: [email protected] Contents ❑ Introduction to Heterospory ❑ Origin of Heterospory ❑ Significance of Heterospory ❑ General accounts of Fossil pteridophytes ❑ Fossil Lycopsids ❑ Fossil Sphenophytes ❑ Fossil Pteridopsis ❑Glossary ❑Assessment Questions ❑Suggested Readings Heterospory and Seed habit Heterospory is a phenomenon in which two kinds of spores are borne by the same plant. The spores differ in size, structure and function. The smaller one is known as microspore and larger one is known as megaspore. Such Pteridophytes are known as heterosporous and the phenomenon is known as heterospory. Most of the Pteridophytes produce one kind of similar spores, Such Peridophytes are known as homosporous and this phenomenon is known as homospory. The sporangia show greater specialization. They are differentiated into micro and megasporangia. The microsporangia contaion microspores whereas megasporangia contain megaspores. The production of two types of sproes with different sexuality was first evolved in pteridophytes. Even though, the condition of heterospory is now represented only by eight living species of pteridophytes, they are Selaginella, Isoetes, Marsilea, Salvinia, Azolla, Regnellidium, Pilularia and Stylites. Origin of heterospory The fossil and developmental studies explain about the origin of heterospory. A number of fossil records proved that heterospory existed in many genera of Lycopsida, Sphenopsida and Pteropsida. They are very common in late Devonian and early Carboniferous periods. During this period the important heterosporous Licopsids genera were Lepidocarpon, Lepidodemdron, Lipidostrobus, Pleoromea, Sigilariosrobus etc.