Cover Page the Handle

Total Page:16

File Type:pdf, Size:1020Kb

Cover Page the Handle Cover Page The handle http://hdl.handle.net/1887/35731 holds various files of this Leiden University dissertation Author: Mennes, Constantijn Title: Antiquities of the rainforest : evolution of mycoheterotrophic angiosperms growing on Glomeromycota Issue Date: 2015-10-06 Appendix B: Supplementary Figures. 181 Antiquities of the rainforest 182 Sciaphila albescens 1 Sciaphila albescens 4 18S Sciaphila albescens 2 Sciaphila albescens 3 Sciaphila purpurea 1 Sciaphila purpurea 2 Sciaphila nana Andruris sp. Seychellaria madagascariensis Seychellaria africana Triuris hyalina 1 Triuris hyalina 2 Triuris hexophthalma 100 Sciaphila sp. 96 Sciaphila quadribullifera Kupea martinetugei 1 Kihansia sp. Sciaphila ledermannii 2 Sciaphila ledermannii 1 Sciaphila tenella Sciaphila picta Pandanus sp. 2 Pandanus tectorius Pandanus baptistii Pandanus tectorius var. laevis Pandanus pacificus Pandanus labyrinthicus Pandanus veitchii Pandanus furcatus Pandanus stenophyllus Pandanus cf. dubius Pandanus purpurascens Pandanus sp. 1 Pandanus utilis Freycinetia cumingiana 1 100 Freycinetia cumingiana 2 Freycinetia philippinensis 88 Freycinetia sp. 1 94 Freycinetia sp. 3 100 Freycinetia sp. 2 * Pandanus montanus 70 Asplundia cf. venezuelensis Asplundia rigida Dicranopygium atrovirens Carludovica palmata 1 98 Carludovica palmata 2 Ludovia lancifolia 58 Cyclanthus bipartitus Croomia pauciflora 100 Stemona sp. Stemona tuberosa var. ternatensis 66 Pentastemona sumatrana Barbacenia elegans 100 Vellozia elegans 67 Acanthochlamys bracteata Dioscorea rockii Dioscorea communis Trichopus sempervirens Tacca integrifolia Nietneria paniculata Narthecium ossifragum Aletris lutea Orontium aquaticum 0.02 * This clade is not recovered in the ML analysis Fig. S1. Phylogeny of Pandanales based on an ML analysis of the 18S rDNA dataset. Values above branches are Bayesian posterior probabilities (expressed as percentages); those below branches are bootstrap support percentages. The scale bar shows the number of substitutions per site. Clades which are not recovered in the ML analysis, but only in the BI analysis are indicated by a vertical bar. Freycinetia sp. 3 Freycinetia sp. 1 atpA Freycinetia cumingiana 1 Freycinetia sp. 2 Freycinetia cumingiana 2 Freycinetia philippinensis Pandanus montanus Pandanus purpurascens Pandanus utilis Pandanus stenophyllus Pandanus furcatus Pandanus veitchii 67 Pandanus tectorius 68 Pandanus cf. dubius Pandanus labyrinthicus Pandanus sp. 1 Pandanus pacificus Pandanus baptistii Pandanus sp. 2 54 Pandanus tectorius var. laevis Asplundia rigida ** 99 Asplundia cf. venezuelensis 78 Ludovia lancifolia 93 Carludovia palmata 2 60 Dicranopygium atrovirens Carludovica palmata 1 Cyclanthus bipartitus Stemona sp. 100 Croomia pauciflora Stemona tuberosa var. ternatensis 61 Pentastemona sumatrana* Sciaphila albescens 1 Sciaphila albescens 2 Sciaphila albescens 3 Sciaphila purpurea 1 Seychellaria africana Sciaphila nana Sciaphila sp. 99 Sciaphila quadribullifera 71 Triuris hyalina 1 Triuris hyalina 2 Lacandonia schismatica Sciaphila picta 100 Sciaphila ledermannii 2 96 Sciaphila ledermannii 1 Kupea martinetugei 2 Kupea martinetugei 1 Kihansia sp. Vellozia elegans 100 Barbacenia elegans 96 Acanthochlamys bracteata Aletris lutea Nietneria paniculata Narthecium ossifragum Trichopus sempervirens Tacca integrifolia Dioscorea rockii Dioscorea communis Triuris hexophthalma Orontium aquaticum * Pentastemona is embedded in Pandanaceae in the BI analysis 0.01 ** This clade is not recovered in the ML analysis Fig. S2. Phylogeny of Pandanales based on an ML analysis of the mitochondrial atpA dataset. Values above branches are Bayesian posterior probabilities; those below branches are bootstrap support percentages. The scale bar shows the number of substitutions per site. Clades which are not recovered in the ML analysis, but only in the BI analysis are indicated by a vertical bar. 183 Antiquities of the rainforest Pandanus montanus matR Pandanus utilis Pandanus purpurascens Pandanus sp. 2 Pandanus tectorius var. laevis Pandanus baptistii Pandanus tectorius Pandanus veitchii Pandanus pacificus Pandanus stenophyllus Pandanus labyrinthicus Pandanus cf. dubius Pandanus sp. 1 100 Pandanus furcatus Freycinetia cumingiana 2 99 Freycinetia cumingiana 1 Freycinetia philippinensis Freycinetia sp. 2 Freycinetia sp. 3 100 Freycinetia sp. 1 98 Carludovica palmata 2 Carludovica palmata 1 Asplundia rigida Asplundia cf. venezuelensis 100 Dicranopygium atrovirens Ludovia lancifolia 85 Cyclanthus bipartitus Sciaphila albescens 4 Sciaphila albescens 3 Sciaphila albescens 1 Sciaphila albescens 2 Sciaphila purpurea 2 Sciaphila purpurea 1 100 Seychellaria madagascariensis 87 Sciaphila nana Seychellaria africana Andruris sp. Sciaphila ledermannii 1 Sciaphila ledermannii 2 Triuris hexophthalma Triuris hyalina 1 Sciaphila sp. 100 Sciaphila quadribullifera 100 Sciaphila picta 99 Sciaphila tenella 100 Kupea martinetugei 1 100 Kupea martinetugei 2 Kihansia sp. 75 Stemona tuberosa var. ternatensis Stemona sp. 100 Croomia pauciflora 99 Pentastemona sumatrana 100 Barbacenia elegans 100 Vellozia elegans Nietneria paniculata Narthecium ossifragum Aletris lutea Dioscorea rockii Dioscorea communis Trichopus sempervirens Tacca integrifolia Orontium aquaticum Fig. S3. Phylogeny of Pandanales based on0.02 an ML analysis of the mitochondrial matR dataset. Values above branches are Bayesian posterior probabilities; those below branches are bootstrap support percentages. The scale bar shows the number of substitutions per site. Pandanus furcatus nad1b-c Pandanus sp. 1 Pandanus veitchii Pandanus tectorius var. laevis Pandanus labyrinthicus Pandanus stenophyllus Pandanus sp. 2 Pandanus utilis Pandanus tectorius Pandanus cf. dubius Pandanus montanus Pandanus baptistii 82 Pandanus purpurascens 57 Pandanus pacificus Freycinetia sp. 1 Freycinetia sp. 3 Freycinetia cumingiana 2 Freycinetia philippinensis Freycinetia cumingiana 1 Freycinetia sp. 2 Asplundia cf. venezuelensis Asplundia rigida Dicranopygium atrovirens Ludovia lancifolia 98 Carludovica palmata 1 88 Carludovica palmata 2 Cyclanthus bipartitus 92 Sciaphila albescens 3 Sciaphila albescens 1 71 Sciaphila purpurea 1 64 Sciaphila ledermannii 2 Sciaphila ledermannii 1 64 Kihansia sp. Kupea martinetugei 1 Stemona sp. 98 Stemona tuberosa var. ternatensis 61 Pentastemona sumatrana Sciaphila nana Nietneria paniculata Narthecium ossifragum 87 Aletris lutea 53 100 Barbacenia elegans 100 Vellozia elegans Dioscorea rockii Dioscorea communis Tacca integrifolia Trichopus sempervirens Orontium aquaticum 0.06 Fig. S4. Phylogeny of Pandanales based on an ML analysis of the mitochondrial nad1 b-c intron dataset. Values above branches are Bayesian posterior probabilities; those below branches are bootstrap support percentages. The scale bar shows the number of substitutions per site. 184 Pandanus sp. 2 Complete Pandanus tectorius Pandanus baptistii Pandanus tectorius var. laevis dataset Pandanus purpurascens Pandanus utilis Pandanus montanus Pandanus sp. 1 Pandanus furcatus Pandanus veitchii Pandanus stenophyllus Pandanus labyrinthicus 100 Pandanus pacificus Pandanus cf. dubius 100 Freycinetia cumingiana 2 Freycinetia philippinensis Freycinetia cumingiana 1 Freycinetia sp. 1 100 Freycinetia sp. 3 Freycinetia sp. 2 100 Asplundia cf. venezuelensis Asplundia rigida Dicranopygium atrovirens Carludovica palmata 2 65100 Carludovica palmata 1 51 Ludovia lancifolia 100 Cyclanthus bipartitus Stemona sp. Stemona tuberosa var. ternatensis 100 Croomia pauciflora 100 Pentastemona sumatrana * Sciaphila albescens 2 10086 Sciaphila albescens 1 Sciaphila albescens 4 100 100 Sciaphila albescens 3 100 100 Sciaphila purpurea 2 100 99 Sciaphila purpurea 1 100 100 Sciaphila nana 93 94 76 73 Andruris sp. 10065 96 Seychellaria africana 52 100 Seychellaria madagascariensis 100 100 Sciaphila ledermannii 2 Sciaphila ledermannii 1 86 100 100 Sciaphila sp. 100 Sciaphila quadribullifera 100 92 100 Triuris hyalina 1 100 93 Triuris hyalina 2 100 100 61 100 Triuris hexophthalma 91 Lacandonia73 schismatica 100 97 Sciaphila picta Sciaphila tenella 100 100 100 Kupea martinetugei 1 100 Kupea martinetugei 2 100 Kihansia sp. 100 Barbacenia elegans Vellozia elegans 100 Acanthochlamys bracteata Dioscorea rockii Dioscorea communis Trichopus sempervirens Tacca integrifolia Narthecium ossifragum Nietneria paniculata Aletris lutea Orontium aquaticum 0.02 * This clade is not recovered in the BI analysis Fig. S5. A four-gene ML analysis of Triuridaceae and relatives including several Triuridaceae taxa (in grey) with less than three genes (a portion of this is shown in Fig. 6). Values above branches are Bayesian posterior probabilities; those below branches are Bootstrap support percentages. The scale bar shows the number of substitutions per site. 185 Antiquities of the rainforest Dioscoreales Poales sp. Arecales sp. Zingiberales sp. Commelinales Asparagales 1 100 2 Liliales 100 cf. cf. 100 cf. 100 cf. sp. 1 sp. 2 sp. 1 sp. 2 cf. // Pandanales 100 100 99 sp. 100 sp. sp. Alismatales // Acorales Fig. S6. Phylogeny of Liliales and related monocot orders based on a Bayesian-inference (BI) analysis of a three-locus molecular dataset (nuclear 18S rDNA and mitochondrial atpA and matR), including only Corsia spp. (blue) from Corsiaceae. The grey shaded area shows the Liliales taxa. Values above branches are posterior probabilities (expressed as percentages) resulting from the BI analysis; those below branches are bootstrap support percentages resulting from the maximum-likelihood (ML) analysis. Support values are only given
Recommended publications
  • J.P.M. Van De Meerendonk Leyden) 1
    Triuridaceae J.P.M. van de Meerendonk Leyden) 1 The Triuridaceae 6 and 45 are a small family (c. genera, c. spp.) of very delicate, saprophytic, terrestrial, mostly dark-red coloured herbs growing in the deep shade of everwet tropical forest, entering the subtropics only in Japan and the Bonin Is. They are in Africa confined to restricted in the West and in areas are also continental SoutheastAsia remarkably rare, as yet only known from two localities in Assam and N. Thailand respectively. Fig. 1. The nearest localities to Indo- china and China are in Hainan and Botel Tobago Is. (southeast off Taiwan). In Australia they are only foundin the Bellenden Ker Range in NE. Queensland,showing theiraversion to dry and seasonal climates. their By small stature (10—40 cm), dark colour, and very small flowers they are evasive to collec- the size is which is found in tors; only one reaching some (45—140 cm) Sciaphila purpurea Peru, according to GIESEN mainly in termite nests in hollow trunks. During exploration, trip stops, either for felling or climbing trees, or for culinary or sanitary purposes, offer the best opportunity to observe them. Flowering specimens can probably be found throughout the year, as it appeared that of com- have been in months the mon species such as Sciaphila arfakiana, specimens collected all of year. with Formerly Triuridaceae were usually placed in the affinity Liliaceae by BENTHAM& HOOKER and by ENGLER& PRANTL. HUTCHINSON (1934) raised the family to the order Triuridales, along- side which he also reckoned the which Alismatalesto saprophytic genus Petrosavia, usually was but He accommodated in Liliaceae, deviates fromLiliaceae in having an apocarpous gynoecium.
    [Show full text]
  • A Case Study with Mycoheterotroph Plastomes
    Aberystwyth University Phylogenomic inference in extremis Lam, Vivienne K. Y.; Darby, Hayley; Merckx, Vincent S. F. T.; Lim, Gwynne; Yukawa, Tomohisa; Neubig, Kurt M.; Abbott, J. Richard; Beatty, Gemma E.; Provan, Jim; Gomez, Marybel Soto; Graham, Sean W. Published in: American Journal of Botany DOI: 10.1002/ajb2.1070 Publication date: 2018 Citation for published version (APA): Lam, V. K. Y., Darby, H., Merckx, V. S. F. T., Lim, G., Yukawa, T., Neubig, K. M., Abbott, J. R., Beatty, G. E., Provan, J., Gomez, M. S., & Graham, S. W. (2018). Phylogenomic inference in extremis: A case study with mycoheterotroph plastomes. American Journal of Botany, 105(3), 480-494. https://doi.org/10.1002/ajb2.1070 Document License CC BY-NC-ND General rights Copyright and moral rights for the publications made accessible in the Aberystwyth Research Portal (the Institutional Repository) are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the Aberystwyth Research Portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the Aberystwyth Research Portal Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. tel: +44 1970 62 2400 email: [email protected] Download date: 03.
    [Show full text]
  • PUBLICATIONS for Calendar Year 2004 and RESEARCH PROJECTS LISTS for FY2005
    ILLINOIS NATURAL HISTORY SURVEY PUBLICATIONS for Calendar Year 2004 AND RESEARCH PROJECTS LISTS for FY2005 1 CONTENTS Center for Aquatic Ecology and Conservation ..............................................................3 Scientifi c Publications ..............................................................................................3 Technical Reports .....................................................................................................4 Miscellaneous ..........................................................................................................6 CAEC Research Projects .........................................................................................7 Center for Biodiversity ................................................................................................10 Scientifi c Publications ............................................................................................10 Technical Reports ...................................................................................................12 Miscellaneous ........................................................................................................13 CBD Research Projects ..........................................................................................15 Center for Ecological Entomology ..............................................................................19 Scientifi c Publications ............................................................................................19 Technical Reports ...................................................................................................21
    [Show full text]
  • First Record of the Mycoheterotrophic Plant Sciaphila Corniculata
    ISSN 1346-7565 Acta Phytotax. Geobot. 69 (1): 69–74 (2018) doi: 10.18942/apg.201717 SHORT COMMUNICATION First Record of the Mycoheterotrophic Plant Sciaphila corniculata (Triuridaceae) from Ishigaki Island, Ryukyu Islands, Japan, with Updated Description of its Morphology, in particular on Stylar Characteristics 1,* 2 KENJI SUETSUGU AND TAKAOMI SUGIMOTO 1Department of Biology, Graduate School of Science, Kobe University, 1-1 Rokkodai, Nada-ku, Kobe, 657-8501, Japan. *[email protected] (author for correspondence); 2Entomological Laboratory, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Hakozaki 6-10-1, Higashi-ku, Fukuoka 812-8581, Japan We report three new localities of the mycoheterotrophic plant Sciaphila corniculata (Triuridaceae) from Ishigaki Island, Ryukyu Islands, Japan. Previously, S. corniculata was reported only from Kolombang- ara Island (Solomon Islands), Waigeo Island (New Guinea) and Obi and Aru islands (the Moluccas). We also update a description of its morphology, in particular on stylar characteristics based on new materi- als. A key to the Japanese species of Sciaphila based on total flower and stylar characteristics is also pro- vided for easy identification of these rare mycoheterotrophic plants. Key words: Distribution, mycoheterotrophy, Sciaphila, taxonomy, Triuridaceae The Triuridaceae comprise fully mycohetero- small, up to 40 cm tall, recognizable only during trophic plants that mainly grow in deep shade un- the reproductive season and usually occur in derstory in ever-wet forests in the tropics and small populations. Consequently, they have subtropics worldwide, reaching their northern- scarcely been collected and their morphological most limits in temperate regions of Japan (van de traits rarely described in detail. In addition, key Meerendonk 1984).
    [Show full text]
  • 90004637.Pdf
    Kobe University Repository : Kernel First Record of the Mycoheterotrophic Plant Sciaphila corniculata from タイトル Ishigaki Island, Ryukyu Islands, Japan, with Updated Description of its Title Morphology, in particular on Stylar Characteristics 著者 Suetsugu, Kenji / Sugimoto, Takaomi Author(s) 掲載誌・巻号・ページ Acta Phytotaxonomica et Geobotanica,69(1):63-67 Citation 刊行日 2018-03-02 Issue date 資源タイプ Journal Article / 学術雑誌論文 Resource Type 版区分 author Resource Version 権利 Copyright ©2018 Japanese Society for Plant Systematics. All Rights Rights Reserved. DOI 10.18942/apg.201716 JaLCDOI URL http://www.lib.kobe-u.ac.jp/handle_kernel/90004637 PDF issue: 2021-10-05 1 Corresponding author: 2 Kenji Suetsugu 3 Mailing address: Department of Biology, Graduate School of Science, Kobe University, 4 1-1 Rokkodai, Nada-ku, Kobe, 657-8501, Japan. 5 Phone number: +81-75-753-6853 6 Fax number: +81-75-753-6722 7 Email: [email protected] 8 Title: First record of the mycoheterotrophic plant Sciaphila corniculata (Triuridaceae) 9 from Ishigaki Island, Ryukyu Islands, Japan, with updated description of its morphology, 10 in particular on stylar characteristics 11 12 Number of table 0 and figure 2 13 Running title: Suetsugu & Sugimoto | Sciaphila corniculata, new to Japan. 14 15 16 17 18 19 20 21 22 23 24 25 1 1 2 Short Communication 3 4 First Record of the Mycoheterotrophic Plant Sciaphila corniculata (Triuridaceae) 5 from Ishigaki Island, Ryukyu Islands, Japan, with updated description of its 6 morphology, in particular on stylar characteristics 7 8 KENJI SUETSUGU1,* and TAKAOMI SUGIMOTO2 9 10 1Department of Biology, Graduate School of Science, Kobe University, 1-1 Rokkodai, 11 Nada-ku, Kobe, 657-8501, Japan.
    [Show full text]
  • The Highly Reduced Plastome of Mycoheterotrophic Sciaphila (Triuridaceae) Is Colinear with Its Green Relatives and Is Under Strong Purifying Selection
    GBE The Highly Reduced Plastome of Mycoheterotrophic Sciaphila (Triuridaceae) Is Colinear with Its Green Relatives and Is under Strong Purifying Selection Vivienne K.Y. Lam1,2,y, Marybel Soto Gomez1,2,y, and Sean W. Graham1,2,* 1Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada 2UBC Botanical Garden & Centre for Plant Research, University of British Columbia, Vancouver, British Columbia, Canada *Corresponding author: E-mail: [email protected]. yThese authors contributed equally to this work. Accepted: July 8, 2015 Data deposition: The genomes and gene sequences have been deposited at GenBank under the accession numbers KP462882, KR902497, and KT204539-KT205273. Abstract The enigmatic monocot family Triuridaceae provides a potentially useful model system for studying the effects of an ancient loss of photosynthesis on the plant plastid genome, as all of its members are mycoheterotrophic and achlorophyllous. However, few studies have placed the family in a comparative context, and its phylogenetic placement is only partly resolved. It was also unclear whether any taxa in this family have retained a plastid genome. Here, we used genome survey sequencing to retrieve plastid genome data for Sciaphila densiflora (Triuridaceae) and ten autotrophic relatives in the orders Dioscoreales and Pandanales. We recovered a highly reduced plastome for Sciaphila that is nearly colinear with Carludovica palmata, a photosynthetic relative that belongs to its sister group in Pandanales, Cyclanthaceae–Pandanaceae. This phylogenetic placement is well supported and robust to a broad range of analytical assumptions in maximum-likelihood inference, and is congruent with recent findings based on nuclear and mitochondrial evidence. The 28 genes retained in the S.
    [Show full text]
  • Sciaphila Lambirensis (Triuridaceae), a New Mycoheterotrophic Plant from Sarawak, Orneo, Malaysia
    ISSN 1346-7565 Acta Phytotax. Geobot. 69 (3): 175–180 (2018) doi: 10.18942/apg.201805 Sciaphila lambirensis (Triuridaceae), a New Mycoheterotrophic Plant from Sarawak, orneo, Malaysia KenJi suetsugu epatment o ioloy Gaduate School o Science obe niesity - oodai ada-u obe yoo - apan. eni.suetsuumail.com Borneo is known to harbor the greatest species diversity of the mycoheterotrophic genus Sciaphila (Tri- uridaceae) and is home to 11 species, including fve endemics. Here, another undescribed Sciaphila spe- cies, S. lambiensis, which was discovered during a botanical survey in Lambir Hills National Park (Sar- awak, Borneo, Malaysia) is reported along with a detailed morphological account. Sciaphila lambiensis is similar to S. beistyla in having six equal perianth segments with a swollen apex bearing long hairs in both staminate and carpellate fowers. However, it is easily distinguishable by the secund arrangement of the fowers and the pedicel slightly recurved at its apex. A key to the species of Sciaphila in Borneo is provided. Key words: Lambir Hills National Park, mycoheterotrophy, new species, taxonomy The Triuridaceae Gardner are a group of fully Furthermore, key characters of the staminate mycoheterotrophic plants of deep shade in the fowers, which are crucial for precise identifca- understory of ever-wet forests in the tropics and tion, have not been documented for some species, subtropics worldwide, reaching their northern- especially if individual specimens were too most limits in Japan (van de Meerendonk 1984). young at the time of collection (Tsukaya & Okada The genus Sciaphila Blume, which contains ca. 2013, Tsukaya & Suetsugu 2014). Given such dif- 40 species, is the largest group within the family fculty of precise species identifcation, the tax- (van de Meerendonk 1984).
    [Show full text]
  • Sciaphila Secundiflora Thwaites Ex Benth. (Triuridaceae): an Unrecorded Species from Korean Flora
    pISSN 1225-8318 Korean J. Pl. Taxon. eISSN 2466-1546 47(3): 196−198 (2017) Korean Journal of https://doi.org/10.11110/kjpt.2017.47.3.196 Plant Taxonomy Sciaphila secundiflora Thwaites ex Benth. (Triuridaceae): An unrecorded species from Korean flora Eun-Young Yim, Hwa-Ja Hyun, Chang-Uk Kim1 and Chan-Soo Kim* Warm Temperate and Subtropical Forest Research Center, National Institute of Forest Science, Seogwipo 63582, Korea 1Jeju Wild Flower, Private Nonprofit Organization, Seogwipo 63582, Korea (Received 2 September 2017; Revised 11 September 2017; Accepted 20 September 2017) ABSTRACT: Sciaphila secundiflora occurs on Jeju Island as a second species of the genus Sciaphila in Korea. This is an important finding in relation to the flora of Korea, as species of the genus Sciaphila are concentrated mainly in Indonesia and Malaysia. Few species are found on the mainland of Asia, in Japan, Taiwan, China (Hainan), tropical Africa, Australia, and on the Pacific islands. In this paper, the species S. secundiflora is described and illustrated as a new record from Korea. In addition, we suggest that the species of the genus Sciaphila should be protected with regard to its habitat characteristics and for its phytogeographic and climatic significance. Keywords: Sciaphila, first record, saprophytic herb, indicator species The family Triuridaceae Gardner includes nine genera with at Hannam-ri, Namwon-eup, Seogwipo-si, Jeju Special Self- approximately 55 species (Christenhusz and Byng, 2016). All Governing Province, Korea. Its presence was reconfirmed on species of Triuridaceae are the mycoheterotrophic plants with 13 Jul 2017 at same site. Voucher specimens of S. secundiflora tiny flowers and reduced scale-like leaves.
    [Show full text]
  • Genome Size Dynamics and Evolution in Monocots
    Hindawi Publishing Corporation Journal of Botany Volume 2010, Article ID 862516, 18 pages doi:10.1155/2010/862516 Review Article Genome Size Dynamics and Evolution in Monocots Ilia J. Leitch,1 Jeremy M. Beaulieu,2 Mark W. Chase,1 Andrew R. Leitch,3 and Michael F. Fay1 1 Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AD, UK 2 Department of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06511, USA 3 School of Biological and Chemical Sciences, Queen Mary University of London, E1 4NS, UK Correspondence should be addressed to Ilia J. Leitch, [email protected] Received 7 January 2010; Accepted 8 March 2010 Academic Editor: Johann Greilhuber Copyright © 2010 Ilia J. Leitch et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Monocot genomic diversity includes striking variation at many levels. This paper compares various genomic characters (e.g., range of chromosome numbers and ploidy levels, occurrence of endopolyploidy, GC content, chromosome packaging and organization, genome size) between monocots and the remaining angiosperms to discern just how distinctive monocot genomes are. One of the most notable features of monocots is their wide range and diversity of genome sizes, including the species with the largest genome so far reported in plants. This genomic character is analysed in greater detail, within a phylogenetic context. By surveying available genome size and chromosome data it is apparent that different monocot orders follow distinctive modes of genome size and chromosome evolution.
    [Show full text]
  • Global Flora Vol 4
    THE GLOBAL FLORA © 2018 Plant Gateway Ltd. A practical flora to vascular plant species of the world ISSN 2398-6336 eISSN 2398-6344 www.plantgateway.com/globalflora/ eISBN 978-0-9929993-6-0 i Published online 9 February 2018 PLANT GATEWAy’s THE GLOBAL FLORA A practical flora to vascular plant species of the world GLOVAP Nomenclature Part 1 February 2018 The Global Flora A practical flora to vascular plant species of the world Special Edition, GLOVAP Nomenclature Part 1, Vol. 4: 1-155. Published by Plant Gateway Ltd., 5 Baddeley Gardens, Bradford, BD10 8JL, United Kingdom © Plant Gateway 2018 This work is in copyright. Subject to statutory exception and to the provision of relevant col- lective licensing agreements, no reproduction of any part may take place without the written permission of Plant Gateway Ltd. ISSN 2398-6336 eISSN 2398-6344 ISBN 978-0-9929993-5-3 eISBN 978-0-9929993-6-0 Plant Gateway has no responsibility for the persistence or accuracy of URLS for external or third-party internet websites referred to in this work, and does not guarantee that any con- tent on such websites is, or will remain, accurate or appropriate. British Library Cataloguing in Publication data A Catalogue record of this book is available from the British Library For information or to purchase other Plant Gateway titles please visit www.plantgateway.com Cover image: Hakea plurijuga (F.Muell.) Christenh. & Byng © Maarten Christenhusz Editors Maarten J.M. Christenhusz Plant Gateway, Bradford & Kingston, United Kingdom and Den Haag, the Netherlands Royal Botanic Gardens, Kew, United Kingdom. [email protected] Michael F.
    [Show full text]
  • Resurrection and Emended Description of Sciaphila Major (Triuridaceae)
    Phytotaxa 459 (1): 025–038 ISSN 1179-3155 (print edition) https://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2020 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.459.1.3 Resurrection and emended description of Sciaphila major (Triuridaceae) KENJI SUETSUGU1,7*, MARTIN DANČÁK2,8*, MICHAL HRONEŠ3,9, AKIYO NAIKI4,10, SHUICHIRO TAGANE5,11 & TETSUKAZU YAHARA6,12 1Department of Biology, Graduate School of Science, Kobe University, 1-1 Rokkodai, Nada-ku, Kobe, 657-8501, Japan 2 Department of Ecology and environmental sciences, Faculty of Science, Palacký University Olomouc, Šlechtitelů 27, 78371 Olomouc, Czech Republic 3Department of Botany, Faculty of Science, Palacký University Olomouc, Šlechtitelů 27, 78371 Olomouc, Czech Republic 4Tropical Biosphere Research Center, University of the Ryukyus, 870 Uehara, Taketomi-cho, Yaeyama-gun, Okinawa 907-1541, Japan 5The Kagoshima University Museum, Kagoshima University, 1-21-30 Korimoto, Kagoshima, 890-0065, Japan 6Department of Biology, Kyushu University, 744 Motooka, Fukuoka, 819-0395, Japan 7 [email protected]; https://orcid.org/0000-0002-7943-4164 8 [email protected]; https://orcid.org/0000-0002-3851-4969 9 [email protected]; https://orcid.org/0000-0002-0380-929X 10 [email protected]; https://orcid.org/0000-0002-3235-2823 11 [email protected]; https://orcid.org/0000-0002-1974-7329 12 [email protected]; https://orcid.org/0000-0001-5105-7152 *Corresponding author: [email protected] (KS), [email protected] (MD) Abstract This paper presents a re-evaluation of the taxonomic identity of Sciaphila major described from Sarawak, Borneo, Malaysia which has been considered conspecific with S.
    [Show full text]
  • Sciaphila Sugimotoi (Triuridaceae), a New Mycoheterotrophic Plant from Ishigaki Island, Japan
    Phytotaxa 314 (2): 279–284 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2017 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.314.2.10 Sciaphila sugimotoi (Triuridaceae), a new mycoheterotrophic plant from Ishigaki Island, Japan KENJI SUETSUGU1* & TATSUKI NISHIOKA2 1Department of Biology, Graduate school of Science, Kobe University, 1-1 Rokkodai, Nada-ku, Kobe, 657-8501, Japan 2Faculty of Agriculture, Kyoto University, Kitashirakawa-Oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan *author for correspondence, [email protected] Abstract A new species of Sciaphila (Triuridaceae), S. sugimotoi Suetsugu & T. Nishioka, is described and illustrated from Ishigaki Island, Okinawa Prefecture, Japan. The new species is similar to S. arfakiana in having a stipitate globose to ellipsoid knob without hairs in apices of all male perianth segments. However, it is clearly distinguishable by its shorter pedicel, filament- connective not extended and thick stem. A key to the Japanese Sciaphila based on the whole flower characteristics and stylar characteristics, are provided for easy identification of these rare mycoheterotrophic plants. Keywords: Distribution, mycoheterotrophic plants, new species, Sciaphila, taxonomy, Triuridaceae, Ryukyu Introduction The Triuridaceae is a family of fully mycoheterotrophic plants that grow in the deep shade of pantropical ever-wet forests throughout the subtropical and temperate regions of Argentina, Paraguay, and Japan (Maas-van de Kamer & Weustenfeld 1998, van de Meerendonk 1984). Recent molecular phylogenetic studies have shown that the Triuridaceae, which comprises approximately 50 species within 11 genera, constitute a single clade within the Pandanales (Davis et al. 2004, Mennes et al.
    [Show full text]