Phylogenetic Structure Analysis Based on Blue Light

Total Page:16

File Type:pdf, Size:1020Kb

Phylogenetic Structure Analysis Based on Blue Light Phylogenetic Structure Analysis Based on Blue Light Receptor Cryptochrome: Insights into How Light Shape the Vertical Structure of Forest Community Qiming Mei1, Ju-Yu Lian1, Yue Wang1, Meng Li1, Xujun Gui1, Zheng-Feng Wang1, Hong-Lin Cao1, and Wan-Hui Ye1 1South China Botanical Garden, Chinese Academy of Sciences October 13, 2020 Abstract Light-regime variability is an important environmental factor which shapes a forest community. So far, none focused on the phylogenetic pattern of plant light receptors, which reflects how genes' evolution influences the coexistence of species in a community. In this study, we analyzed community phylogenetic structure of the south subtropical forest by sequences of plant blue light receptor cryptochrome (CRY) and compared the results of DNA barcodes. Patterns of community assembly was estimated by net relatedness index (NRI) and nearest taxon index (NTI). We found that CRY showed quite different phylogenetic structure as compared to DNA barcoding results, all habitats displayed consistent phylogenetic structure patterns, suggesting a convergent evolution of light sensing system of plant in local adaptation. Also, both NRI and NTI values increased through the time, indicating that the phylogenetic structure of tree community became more overdispersion as succession proceeds; phylogenetic closely-related species tended to co-occur and environmental filtering played a more important role in the community assembly. Furthermore, phylogenetic patterns were more clustering in upper canopy layers, and NTI values of all canopy layers were above zero, suggesting that phylogenetically related species tended to coexist and adapted to similar light conditions. Hosted file Manuscript.pdf available at https://authorea.com/users/366771/articles/486413-phylogenetic- structure-analysis-based-on-blue-light-receptor-cryptochrome-insights-into-how-light- shape-the-vertical-structure-of-forest-community Posted on Authorea 13 Oct 2020 | The copyright holder is the author/funder. All rights reserved. No reuse without permission. | https://doi.org/10.22541/au.160257635.51966646/v1 | This a preprint and has not been peer reviewed. Data may be preliminary. 1 (a) (b) Habitat 500 400 Low valley Low slope 300 High valley Westing (m) Westing 200 Ridge High slope 100 0 0 100 200 300 400 Southing (m) 1.00 Myrtales Myrtales 1.00 Sapindales Sapindales 0.95 Malvales 1.00 1.00 Malvales 0.98 Oxalidales 1.00 Oxalidales 0.80 0.86 Malpighiales Malpighiales 0.98 1.00 Fabales Fagales 1.00 1.00 Fabales 0.64 Fagales 0.86 1.00 Rosales Rosales Saxifragales Saxifragales 1.00 Gentianales 0.65 Gentianales 0.97 Apiales Apiales 0.55 0.99 1.00 Aquifoliales Aquifoliales 1.00 0.90 1.00 Ericales Ericales 1.00 Proteales 0.62 Proteales Proteales Proteales Magnoliales Magnoliales 0.99 1.00 Laurales Laurales 1.00 Monocots Monocots 10 10 (a) (b) Posted on Authorea 13 Oct 2020 | The copyright holder is the author/funder. All rights reserved. No reuse without permission. | https://doi.org/10.22541/au.160257635.51966646/v1 | This a preprint and has not been peer reviewed. Data may be preliminary. 2 5.0 5.0 5.0 a b a,b a b a b b a c 2.5 2.5 2.5 b,c c b c b,c c NRI NRI c NRI c c b,c 0.0 0.0 0.0 −2.5 −2.5 −2.5 HG* HS LS* RT V* HG HS LS* RT V* HG* HS* LS* RT* V* Habitat Habitat Habitat (a) (b) (c) 3 c 3 3 b,c b b a b a b a a a,b a c a a,b a 2 2 a a a b 2 a a a a b 1 1 1 NTI NTI NTI 0 0 0 −1 −1 −1 Method −2 −2 −2 Barcode CRY HG* HS LS* RT V* HG* HS* LS* RT* V* HG* HS* LS* RT V* Habitat Habitat Habitat (d) (e) (f) 2 2 1 1 NTI NRI 0 0 −1 Method −1 Barcode 2005* 2010* 2015* 2005* 2010* 2015* Year Year CRY Posted on Authorea 13 Oct 2020 | The copyright holder is the author/funder. All rights reserved. No reuse without permission. | https://doi.org/10.22541/au.160257635.51966646/v1 | This a preprint and has not been peer reviewed. Data may be preliminary. 3 # # # # # # # # # # # 2.5 # 2.5 2.5 NRI NRI NRI 0.0 0.0 0.0 −2.5 −2.5 −2.5 ES* LS ES* LS* ES* LS* Succession Succession Succession (a) (b) (c) # # # # # # 2 2 2 0NTI 0NTI 0NTI −2 −2 −2 Method Barcode CRY ES* LS* ES* LS* ES* LS* Succession Succession Succession (d) (e) (f) Posted on Authorea 13 Oct 2020 | The copyright holder is the author/funder. All rights reserved. No reuse without permission. | https://doi.org/10.22541/au.160257635.51966646/v1 | This a preprint and has not been peer reviewed. Data may be preliminary. 4 a 4 4 b b a,b a,b a a,b b b a a a b b a c 2 2 NRI NRI 0 0 −2 −2 Sh* Un Ca Em* Sh* Un* Ca Em* Layer Layer (a) (b) b c b a 2 2 b b a b c c a b 0 0 NTI NTI −2 −2 −4 −4 Method Barcode Sh* Un* Ca* Em* Sh* Un* Ca* Em* CRY Layer Layer (c) (d) Posted on Authorea 13 Oct 2020 | The copyright holder is the author/funder. All rights reserved. No reuse without permission. | https://doi.org/10.22541/au.160257635.51966646/v1 | This a preprint and has not been peer reviewed. Data may be preliminary. 5.
Recommended publications
  • Clase 9 Magnoliidae-2015.Pdf
    Origen y Clasificación de las Angiospermas Son un grupo natural? Cuáles son las novedades evolutivas de las plantas con flor? Cuándo y dónde se originó el grupo? Cuáles son sus antecesores? Cómo eran las primeras plantas con flor? Cuáles son las relaciones con las restantes plantas vasculares? Dra. Susana E. Freire Prof. Titular - Botánica Sistemática II Fac. de Cs. Naturales y Museo, UNLP Filogenia de las Tracheophyta Progymnospermopsidas “Gimnospermae” † † † † Angiospermas Pteridospermopsidas Pinopsidas Rhyniopsidas Lycopsidas Psilophyton Monilophytas Gnetopsidas Gynkgopsidas Cycadopsidas Aneurophyytales Archaeopteridales Hojas retinervadas Doble fecundación / Endosperma Xilema con vasos Tubos cribos con células anexas semilla Óvulos con 2 tegumentos Carpelos cerrados heterosporía + Gametofitos reducidos xilema 2rio + Microsporofilos con 4 sacos polínicos megáfilos Perianto zoofilo ramificación monopodial traqueidas fuertemente engrosadas traqueidas Modificado de Judd et al 2002. Origen de las Angiospermas 130 millones de años Lugar y tiempo de Origen de las Angiospermas 130 millones de años a bajas latitudes Flora del Cretácico Bosques montañosos tropicales: (a) Araucaria (b) Taxodiáceas (c) Cycadáceas (d) Cycadeoideales (a) (e) Lycópsidas (h) (f) Helechos (g) Angiospermas (sa) (h) Angiospermas (h) (i) Gnetópsidas (h, a) (j) Angiospermas (A) Antecesores de las Angiospermas deAntecesores las Lyginopteridales s s e a a l s s i t a a m e r y t l r d e i h y a s t e a o p h s a p p i r o e o o p s o n l e g d d o s o f o u t i k í a t a
    [Show full text]
  • Heterodichogamy.Pdf
    Research Update TRENDS in Ecology & Evolution Vol.16 No.11 November 2001 595 How common is heterodichogamy? Susanne S. Renner The sexual systems of plants usually Heterodichogamy differs from normal (Zingiberales). These figures probably depend on the exact spatial distribution of dichogamy, the temporal separation of underestimate the frequency of the gamete-producing structures. Less well male and female function in flowers, in heterodichogamy. First, the phenomenon known is how the exact timing of male and that it involves two genetic morphs that is discovered only if flower behavior is female function might influence plant occur at a 1:1 ratio. The phenomenon was studied in several individuals and in mating. New papers by Li et al. on a group discovered in walnuts and hazelnuts5,6 natural populations. Differential of tropical gingers describe differential (the latter ending a series of Letters to movements and maturation of petals, maturing of male and female structures, the Editor about hazel flowering that styles, stigmas and stamens become such that half the individuals of a began in Nature in 1870), but has gone invisible in dried herbarium material, population are in the female stage when almost unnoticed7. Indeed, its recent and planted populations deriving from the other half is in the male stage. This discovery in Alpinia was greeted as a vegetatively propagated material no new case of heterodichogamy is unique new mechanism, differing ‘from other longer reflect natural morph ratios. The in involving reciprocal movement of the passive outbreeding devices, such as discovery of heterodichogamy thus styles in the two temporal morphs. dichogamy…and heterostyly in that it depends on field observations.
    [Show full text]
  • A Case Study Based on the Wondrous Order Plants Table
    Highly competitive – he has to be in first place, it is very important to him, to be number one – with his siblings in particu- A Case Study Based lar, even though he is younger than they are. When his siblings fight he tells them – he is friends with both of them. On the one on the Wondrous hand he competes with them and on the other, it is highly important that everyone likes him. Should one brother tell him, “I Order Plants Table am not your friend”–he wants to die. This really threatens him. It is highly important Michal Yakir, Israel that they will not be angry with him. If I am angry with him – he is worried about it, from a young age”. Case of a Child Suffering cool and gets along with everything. He He is short for his age. has no anxieties during day-to-day life. He MATERIA MEDICA AND CASES from Ear Infections was always a calm child, and this is why I Cravings: Sweets (3) especially lollipops, decided to have yet another baby… but purple, pink and red ones. He likes to eat This is a case study of a four-year-old child, perhaps, something which is suppressed chocolate and cheese. Otherwise he is not arriving with his mother for a first consul- during the day surfaces at night? During much of an eater. tation on 28.4.10. the day he is calm, but a medium we con- sulted suggested his anxieties are related He is not fond of tomatoes (recently) and Observation: a delicate looking child, with with a past life.
    [Show full text]
  • European Academic Research
    EUROPEAN ACADEMIC RESEARCH Vol. IV, Issue 10/ January 2017 Impact Factor: 3.4546 (UIF) ISSN 2286-4822 DRJI Value: 5.9 (B+) www.euacademic.org Evidences from morphological investigations supporting APGIII and APGIV Classification of the family Apocynaceae Juss., nom. cons IKRAM MADANI Department of Botany, Faculty of Science University of Khartoum, Sudan LAYALY IBRAHIM ALI Faculty of Science, University Shandi EL BUSHRA EL SHEIKH EL NUR Department of Botany, Faculty of Science University of Khartoum, Sudan Abstract: Apocynaceae have traditionally been divided into into two subfamilies, the Plumerioideae and the Apocynoideae. Recently, based on molecular data, classification of Apocynaceae has undergone considerable revisions. According to the Angiosperm Phylogeny Group III (APGIII, 2009), and the update of the Angiosperm Phylogeny Group APG (APGIV, 2016) the family Asclepiadaceae is now included in the Apocynaceae. The family, as currently recognized, includes some 1500 species divided in about 424 genera and five subfamilies: Apocynoideae, Rauvolfioideae, Asclepiadoideae, Periplocoideae, and Secamonoideae. In this research selected species from the previous families Asclepiadaceae and Apocynaceae were morphologically investigated in an attempt to distinguish morphological important characters supporting their new molecular classification. 40 morphological characters were treated as variables and analyzed for cluster of average linkage between groups using the statistical package SPSS 16.0. Resulting dendrograms confirm the relationships between species from the previous families on the basis of their flowers, fruits, 8259 Ikram Madani, Layaly Ibrahim Ali, El Bushra El Sheikh El Nur- Evidences from morphological investigations supporting APGIII and APGIV. Classification of the family Apocynaceae Juss., nom. cons and seeds morphology. Close relationships were reported between species from the same subfamilies.
    [Show full text]
  • Phylogenomic Approach
    Toward the ultimate phylogeny of Magnoliaceae: phylogenomic approach Sangtae Kim*1, Suhyeon Park1, and Jongsun Park2 1 Sungshin University, Korea 2 InfoBoss Co., Korea Mr. Carl Ferris Miller Founder of Chollipo Arboretum in Korea Chollipo Arboretum Famous for its magnolia collection 2020. Annual Meeting of Magnolia Society International Cholliop Arboretum in Korea. April 13th~22th, 2020 http://WWW.Chollipo.org Sungshin University, Seoul, Korea Dr. Hans Nooteboom Dr. Liu Yu-Hu Twenty-one years ago... in 1998 The 1st International Symposium on the Family Magnoliaceae, Gwangzhow Dr. Hiroshi Azuma Mr. Richard Figlar Dr. Hans Nooteboom Dr. Qing-wen Zeng Dr. Weibang Sun Handsome young boy Dr. Yong-kang Sima Dr. Yu-wu Law Presented ITS study on Magnoliaceae - never published Ten years ago... in 2009 Presented nine cp genome region study (9.2 kbp) on Magnoliaceae – published in 2013 2015 1st International Sympodium on Neotropical Magnoliaceae Gadalajara, 2019 3rd International Sympodium and Workshop on Neotropical Magnoliaceae Asterales Dipsacales Apiales Why magnolia study is Aquifoliales Campanulids (Euasterids II) Garryales Gentianales Laminales Solanales Lamiids important in botany? Ericales Asterids (Euasterids I) Cornales Sapindales Malvales Brassicales Malvids Fagales (Eurosids II) • As a member of early-diverging Cucurbitales Rosales Fabales Zygophyllales Celestrales Fabids (Eurosid I) angiosperms, reconstruction of the Oxalidales Malpighiales Vitales Geraniales Myrtales Rosids phylogeny of Magnoliaceae will Saxifragales Caryphyllales
    [Show full text]
  • Full of Beans: a Study on the Alignment of Two Flowering Plants Classification Systems
    Full of beans: a study on the alignment of two flowering plants classification systems Yi-Yun Cheng and Bertram Ludäscher School of Information Sciences, University of Illinois at Urbana-Champaign, USA {yiyunyc2,ludaesch}@illinois.edu Abstract. Advancements in technologies such as DNA analysis have given rise to new ways in organizing organisms in biodiversity classification systems. In this paper, we examine the feasibility of aligning two classification systems for flowering plants using a logic-based, Region Connection Calculus (RCC-5) ap- proach. The older “Cronquist system” (1981) classifies plants using their mor- phological features, while the more recent Angiosperm Phylogeny Group IV (APG IV) (2016) system classifies based on many new methods including ge- nome-level analysis. In our approach, we align pairwise concepts X and Y from two taxonomies using five basic set relations: congruence (X=Y), inclusion (X>Y), inverse inclusion (X<Y), overlap (X><Y), and disjointness (X!Y). With some of the RCC-5 relationships among the Fabaceae family (beans family) and the Sapindaceae family (maple family) uncertain, we anticipate that the merging of the two classification systems will lead to numerous merged solutions, so- called possible worlds. Our research demonstrates how logic-based alignment with ambiguities can lead to multiple merged solutions, which would not have been feasible when aligning taxonomies, classifications, or other knowledge or- ganization systems (KOS) manually. We believe that this work can introduce a novel approach for aligning KOS, where merged possible worlds can serve as a minimum viable product for engaging domain experts in the loop. Keywords: taxonomy alignment, KOS alignment, interoperability 1 Introduction With the advent of large-scale technologies and datasets, it has become increasingly difficult to organize information using a stable unitary classification scheme over time.
    [Show full text]
  • Computer Vision Cracks the Leaf Code
    Computer vision cracks the leaf code Peter Wilfa,1, Shengping Zhangb,c,1, Sharat Chikkerurd, Stefan A. Littlea,e, Scott L. Wingf, and Thomas Serreb,1 aDepartment of Geosciences, Pennsylvania State University, University Park, PA 16802; bDepartment of Cognitive, Linguistic and Psychological Sciences, Brown Institute for Brain Science, Brown University, Providence, RI 02912; cSchool of Computer Science and Technology, Harbin Institute of Technology, Weihai 264209, Shandong, People’s Republic of China; dAzure Machine Learning, Microsoft, Cambridge, MA 02142; eLaboratoire Ecologie, Systématique et Evolution, Université Paris-Sud, 91405 Orsay Cedex, France; and fDepartment of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013 Edited by Andrew H. Knoll, Harvard University, Cambridge, MA, and approved February 1, 2016 (received for review December 14, 2015) Understanding the extremely variable, complex shape and venation species (15–19), and there is community interest in approaching this characters of angiosperm leaves is one of the most challenging problem through crowd-sourcing of images and machine-identifi- problems in botany. Machine learning offers opportunities to analyze cation contests (see www.imageclef.org). Nevertheless, very few large numbers of specimens, to discover novel leaf features of studies have made use of leaf venation (20, 21), and none has angiosperm clades that may have phylogenetic significance, and to attempted automated learning and classification above the species use those characters to classify unknowns. Previous computer vision level that may reveal characters with evolutionary significance. approaches have primarily focused on leaf identification at the species There is a developing literature on extraction and quantitative level. It remains an open question whether learning and classification analyses of whole-leaf venation networks (22–25).
    [Show full text]
  • Phylogeny of Rosids! ! Rosids! !
    Phylogeny of Rosids! Rosids! ! ! ! ! Eurosids I Eurosids II Vitaceae Saxifragales Eurosids I:! Eurosids II:! Zygophyllales! Brassicales! Celastrales! Malvales! Malpighiales! Sapindales! Oxalidales! Myrtales! Fabales! Geraniales! Rosales! Cucurbitales! Fagales! After Jansen et al., 2007, Proc. Natl. Acad. Sci. USA 104: 19369-19374! Phylogeny of Rosids! Rosids! ! ! ! ! Eurosids I Eurosids II Vitaceae Saxifragales Eurosids I:! Eurosids II:! Zygophyllales! Brassicales! Celastrales! Malvales! Malpighiales! Sapindales! Oxalidales! Myrtales! Fabales! Geraniales! Rosales! Cucurbitales! Fagales! After Jansen et al., 2007, Proc. Natl. Acad. Sci. USA 104: 19369-19374! Alnus - alders A. rubra A. rhombifolia A. incana ssp. tenuifolia Alnus - alders Nitrogen fixation - symbiotic with the nitrogen fixing bacteria Frankia Alnus rubra - red alder Alnus rhombifolia - white alder Alnus incana ssp. tenuifolia - thinleaf alder Corylus cornuta - beaked hazel Carpinus caroliniana - American hornbeam Ostrya virginiana - eastern hophornbeam Phylogeny of Rosids! Rosids! ! ! ! ! Eurosids I Eurosids II Vitaceae Saxifragales Eurosids I:! Eurosids II:! Zygophyllales! Brassicales! Celastrales! Malvales! Malpighiales! Sapindales! Oxalidales! Myrtales! Fabales! Geraniales! Rosales! Cucurbitales! Fagales! After Jansen et al., 2007, Proc. Natl. Acad. Sci. USA 104: 19369-19374! Fagaceae (Beech or Oak family) ! Fagaceae - 9 genera/900 species.! Trees or shrubs, mostly northern hemisphere, temperate region ! Leaves simple, alternate; often lobed, entire or serrate, deciduous
    [Show full text]
  • ABSTRACTS 117 Systematics Section, BSA / ASPT / IOPB
    Systematics Section, BSA / ASPT / IOPB 466 HARDY, CHRISTOPHER R.1,2*, JERROLD I DAVIS1, breeding system. This effectively reproductively isolates the species. ROBERT B. FADEN3, AND DENNIS W. STEVENSON1,2 Previous studies have provided extensive genetic, phylogenetic and 1Bailey Hortorium, Cornell University, Ithaca, NY 14853; 2New York natural selection data which allow for a rare opportunity to now Botanical Garden, Bronx, NY 10458; 3Dept. of Botany, National study and interpret ontogenetic changes as sources of evolutionary Museum of Natural History, Smithsonian Institution, Washington, novelties in floral form. Three populations of M. cardinalis and four DC 20560 populations of M. lewisii (representing both described races) were studied from initiation of floral apex to anthesis using SEM and light Phylogenetics of Cochliostema, Geogenanthus, and microscopy. Allometric analyses were conducted on data derived an undescribed genus (Commelinaceae) using from floral organs. Sympatric populations of the species from morphology and DNA sequence data from 26S, 5S- Yosemite National Park were compared. Calyces of M. lewisii initi- NTS, rbcL, and trnL-F loci ate later than those of M. cardinalis relative to the inner whorls, and sepals are taller and more acute. Relative times of initiation of phylogenetic study was conducted on a group of three small petals, sepals and pistil are similar in both species. Petal shapes dif- genera of neotropical Commelinaceae that exhibit a variety fer between species throughout development. Corolla aperture of unusual floral morphologies and habits. Morphological A shape becomes dorso-ventrally narrow during development of M. characters and DNA sequence data from plastid (rbcL, trnL-F) and lewisii, and laterally narrow in M.
    [Show full text]
  • Angiosperm Clades in the Potomac Group: What Have We Learned Since 1977?
    UC Davis UC Davis Previously Published Works Title Angiosperm clades in the potomac group: What have we learned since 1977? Permalink https://escholarship.org/uc/item/5z89c18z Journal Bulletin of the Peabody Museum of Natural History, 55(2-3) ISSN 0079-032X Authors Doyle, JA Upchurch, GR Publication Date 2014-10-01 DOI 10.3374/014.055.0203 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Angiosperm Clades in the Potomac Group: What Have We Learned since 1977? James A. Doyle1 and Garland R. Upchurch, Jr.2 1 Corresponding author: Department of Evolution and Ecology, University of California, Davis CA 95616 USA —email: [email protected] 2 Department of Biology, Texas State University, San Marcos TX 78666 USA —email: [email protected] ABSTRACT In their 1977 study on Potomac Group angiosperms, Hickey and Doyle made only broad com- parisons with living taxa. Newer data, especially discoveries of fossil flowers in the Potomac and coeval deposits and increasingly robust molecular phylogenies of living angiosperms, allow more precise phylogenetic placement of fossils. Hickey and Doyle compared most early Potomac leaves (Aptian–early Albian) with “magnoliids,” a paraphyletic group as then defined, but several clades can now be recognized. Leaves and dispersed cuticles share epidermal features with woody mem- bers of the basal ANITA grade, and in some cases crown group Austrobaileyales, whose presence is confirmed by flowers called Anacostia. Aptian–Albian flowers (Monetianthus, Carpestella) and whole plants (Pluricarpellatia) are nested in crown group Nymphaeales; Potomac reniform leaves could belong to this clade. Several Potomac leaves have chloranthoid teeth, venation, and oppo- site phyllotaxis consistent with Chloranthaceae, while Aptian to Cenomanian flowers reveal the presence of both crown group Chloranthaceae (Asteropollis plant, near Hedyosmum) and stem relatives of this family and/or Ceratophyllum (Canrightia, Zlatkocarpus, Pennipollis plant, possi- bly Appomattoxia).
    [Show full text]
  • BOT 5725-Taxonomy of Vascular Plants
    BOT 5725 Taxonomy of Vascular Plants Spring 2018 Instructors: Doug Soltis (301 Dickinson; phone: 273-1963; e-mail: [email protected]) Pam Soltis (301 Dickinson; phone: 273-1964; e-mail: [email protected]) Nico Cellinese (379 Dickinson; phone: 273-1979; e-mail: [email protected]) Emily Sessa (521 Bartram; phone: 392-1098; e-mail: [email protected]) Ryan Folk (359 Dickinson; phone: 330-801-3078; email: [email protected]) Office Hours: By appointment Credits: 4 Herbarium: 379 Dickinson Hall: phone: 273-1990. Library is open between 9:00 am and 5:00 pm, but plant collection usage restricted to faculty (or graduate students with approved systematic research projects). Lecture: Tuesday & Thursday, periods 6-9 (12:50-4:55pm); Rolfs Hall room 105. Textbook (required): Christenhusz et al. (2017) Plants of the World. Plus additional readings to be provided as PDFs on Canvas. Laboratory tools: 2 dissecting needles, package of razor blades (or scalpel), tweezers, 10X hand-lens. Grading: One mid-term exam (45% of final grade), one final exam (45% of final exam), class participation (10% of final grade). Grade based on total number of points, with 90% or above an “A”, 89-80% “B”, 79-70% “C”, 69-60% “D”, and below failing; plus and minus grades will be used. Exams will be based on lecture and laboratory material. Outline of lectures and labs Spring 2017 Week 1: 9 Jan PS Introduction: What is taxonomy? Basic principles, digital resources 11 Jan NC 12:50-1:40pm (Rolfs): Field and herbarium methods; identification and introduction to nomenclature 2pm (Dickinson): Herbarium Tour Week 2: 16 Jan NC Species concepts, speciation 18 Jan PS Phylogenetics Week 3: 23 Jan PS Phylogenetics, cont.
    [Show full text]
  • Pan-Plant Ribopool Universal, Efficient Ribosomal RNA Depletion for Flowering Plants (Angiosperms)
    Pan-Plant riboPOOL Universal, Efficient Ribosomal RNA Depletion For Flowering Plants (Angiosperms) Efficient rRNA depletion tool Targets 28S, 18S, 5.8S & 5S rRNA Broad coverage of flowering plants Targets mitochondrial rRNA For leaf, seed & root tissue Targets plastid rRNA The high abundance of ribosomal RNA (rRNA) limits detection efficiency of relevant RNAs of the transcriptome by RNA-Seq. The Pan-Plant riboPOOL offers a universal solution to selectively deplete cytoplasmic (28S, 18S, 5.8S & 5S), plastid and mitochondrial rRNA of flowering plants in leaf, seed and root tissue. Wide Species Coverage of Pan-Plant riboPOOL The Pan-Plant riboPOOL consists of a highly complex mixture of biotinylated oligos, designed to optimally cover major phyla of flowering plants. Liliales The Pan-Plant riboPOOL depletes rRNA Apsparagales Laurales for more than 30 orders: Zingiberales Nymphaeales Poales · Rice · Jatropha · Soy Bean Vitales Magnoliids · Potato · Cotton · Coffee Ranunculales Cucurbitales Monocots Proteales · Carrot · Artichoke · Olive Rosales · Arabidopsis · Corn · Aster Fabales Caryophyllales Eudicots · Wheat · Apple · Orange Rosids Solanales Malpighiales · Buckwheat · and more Asterids Gentianales Lamiales Malvales Asterales Brassicales Myrtales *If your species is not within these phyla, Apiales Sapindales please enquire about our custom riboPOOLs. Data with Pan-Plant riboPOOL – Efficient Across Phyla The Pan-Plant riboPOOL efficiently depleted rRNA (> 91%) when tested on six species of Angiosperms from genera Fabacea, Loasacea, Brassicae and Rosaceae. Remarkably, a species from the primitive Green Algae phyla when tested showed > 80% rRNA depletion efficiency, suggesting that the Pan-Plant riboPOOL may be successfully applied to other phyla aside from Angiosperms. remaining rRNA non-rRNA M. domestica (Rosacea) 3,6% 96,4% T.
    [Show full text]