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LA INFLUENCIA De FRANCISCO HERNÁNDEZ En La CONSTITUCIÓN De La BOTÁNICA MATERIA MÉDICA MODERNAS
JOSÉ MARíA LÓPEZ PIÑERO JOSÉ PARDO TOMÁS LA INFLUENCIA de FRANCISCO HERNÁNDEZ (1515-1587) en la CONSTITUCIÓN de la BOTÁNICA y la MATERIA MÉDICA MODERNAS INSTITUTO DE ESTUDIOS DOCUMENTALES E HISTÓRICOS SOBRE LA CIENCIA UNIVERSITAT DE VALENCIA - C. S. 1. C. VALENCIA, 1996 La influencia de Francisco Hernández (1515·1587) en la constitución de la botánica y la materia médica modernas CUADERNOS VALENCIANOS DE HISTORIA DE LA MEDICINA y DE LA CIENCIA LI SERIE A (MONOGRAFÍAS) JOSÉ MARÍA LÓPEZ PIÑERO JOSÉ PARDO TOMÁS La influencia de Francisco Hernández (1515-1587) en la constitución de la botánica y la materia médica modernas INSTITUTO DE ESTUDIOS DOCUMENTALES E HISTÓRICOS SOBRE LA CIENCIA UNIVERSITAT DE VALENCIA - C.S.I.C. VALENCIA, 1996 IMPRESO EN ESPA~A PRINTED IN SPAIN I.S.B.N. 84-370-2690-3 DEPÓSITO LEGAL: v. 3.795 - 1996 ARTES GRÁFICAS SOLER, S. A. - LA OLlVERETA, 28 - 46018 VALENCIA Sumario Los estudios sobre Francisco Hernández y su obra ...................................... 9 El marco histórico de la influencia de Hernández: la constitución de la botánica y de la materia médica modernas ........................................ 21 Francisco Hernández y su Historia de las plantas de Nueva España .......................................................................................... 35 El conocimiento de las plantas americanas en la Europa de la transición de los siglos XVI al XVII ........................................................... 113 La edición de materiales de la Historia de las plantas de Nueva España durante la primera -
Caryophyllales 2018 Instituto De Biología, UNAM September 17-23
Caryophyllales 2018 Instituto de Biología, UNAM September 17-23 LOCAL ORGANIZERS Hilda Flores-Olvera, Salvador Arias and Helga Ochoterena, IBUNAM ORGANIZING COMMITTEE Walter G. Berendsohn and Sabine von Mering, BGBM, Berlin, Germany Patricia Hernández-Ledesma, INECOL-Unidad Pátzcuaro, México Gilberto Ocampo, Universidad Autónoma de Aguascalientes, México Ivonne Sánchez del Pino, CICY, Centro de Investigación Científica de Yucatán, Mérida, Yucatán, México SCIENTIFIC COMMITTEE Thomas Borsch, BGBM, Germany Fernando O. Zuloaga, Instituto de Botánica Darwinion, Argentina Victor Sánchez Cordero, IBUNAM, México Cornelia Klak, Bolus Herbarium, Department of Biological Sciences, University of Cape Town, South Africa Hossein Akhani, Department of Plant Sciences, School of Biology, College of Science, University of Tehran, Iran Alexander P. Sukhorukov, Moscow State University, Russia Michael J. Moore, Oberlin College, USA Compilation: Helga Ochoterena / Graphic Design: Julio C. Montero, Diana Martínez GENERAL PROGRAM . 4 MONDAY Monday’s Program . 7 Monday’s Abstracts . 9 TUESDAY Tuesday ‘s Program . 16 Tuesday’s Abstracts . 19 WEDNESDAY Wednesday’s Program . 32 Wednesday’s Abstracs . 35 POSTERS Posters’ Abstracts . 47 WORKSHOPS Workshop 1 . 61 Workshop 2 . 62 PARTICIPANTS . 63 GENERAL INFORMATION . 66 4 Caryophyllales 2018 Caryophyllales General program Monday 17 Tuesday 18 Wednesday 19 Thursday 20 Friday 21 Saturday 22 Sunday 23 Workshop 1 Workshop 2 9:00-10:00 Key note talks Walter G. Michael J. Moore, Berendsohn, Sabine Ya Yang, Diego F. Registration -
The Vascular Plants of Massachusetts
The Vascular Plants of Massachusetts: The Vascular Plants of Massachusetts: A County Checklist • First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Somers Bruce Sorrie and Paul Connolly, Bryan Cullina, Melissa Dow Revision • First A County Checklist Plants of Massachusetts: Vascular The A County Checklist First Revision Melissa Dow Cullina, Bryan Connolly, Bruce Sorrie and Paul Somers Massachusetts Natural Heritage & Endangered Species Program Massachusetts Division of Fisheries and Wildlife Natural Heritage & Endangered Species Program The Natural Heritage & Endangered Species Program (NHESP), part of the Massachusetts Division of Fisheries and Wildlife, is one of the programs forming the Natural Heritage network. NHESP is responsible for the conservation and protection of hundreds of species that are not hunted, fished, trapped, or commercially harvested in the state. The Program's highest priority is protecting the 176 species of vertebrate and invertebrate animals and 259 species of native plants that are officially listed as Endangered, Threatened or of Special Concern in Massachusetts. Endangered species conservation in Massachusetts depends on you! A major source of funding for the protection of rare and endangered species comes from voluntary donations on state income tax forms. Contributions go to the Natural Heritage & Endangered Species Fund, which provides a portion of the operating budget for the Natural Heritage & Endangered Species Program. NHESP protects rare species through biological inventory, -
Calligonum Polygonoides Linnaeus Extract: HPLC-EC and Total Antioxidant Capacity Evaluation Sara M
Full Paper DOI: 10.1002/elan.201400555 Calligonum polygonoides Linnaeus Extract: HPLC-EC and Total Antioxidant Capacity Evaluation Sara M. C. Gomes,[a] Isabel P. G. Fernandes,[a] Narpat Singh Shekhawat,[b] Sunita Kumbhat,[c] and Ana Maria Oliveira-Brett*[a] Abstract: Flavonoids in Calligonum polygonoides Lin- pounds. The total antioxidant capacity was quantified naeus extract were separated, detected, and identified by using the DPPHC method and voltammetry. The RP- reverse-phase high-performance liquid chromatography HPLC-EC led to the detection of nine different flavo- (RP-HPLC) with electrochemical detection (EC) in com- noids: catechin, delphinidin, fisetin, myricetin, epicate- bined isocratic and gradient elution using a glassy carbon chin, kuromanin, rutin, callistephin and procyanidin A2, or a boron doped diamond electrode. Ultrasonication in a single run by direct injection of the sample extract coupled with a microwave-assisted technique was devel- solution. oped to optimize the extraction of the phenolic com- Keywords: Calligonum polygonoides Linnaeus · DPPHC method · Electrochemical detection · Flavonoids · Reverse-phase high- performance liquid chromatography 1 Introduction plant has made it vulnerable and endangered species in its habitat [2]. Phenolic compounds constitute one of the most numerous Calligonum polygonoides Linnaeus is known for its me- groups of plant secondary metabolites. The interest in the dicinal properties apart from being traditionally used as bioactivity of phenolic compounds is due to the potential food during frequent famines, Figure 1 [3–6]. These health benefits of these polyphenolic components and plants produce numerous flower buds during March and their involvement in important biological and industrial April. The local people harvest branches bearing on processes. -
Untangling Phylogenetic Patterns and Taxonomic Confusion in Tribe Caryophylleae (Caryophyllaceae) with Special Focus on Generic
TAXON 67 (1) • February 2018: 83–112 Madhani & al. • Phylogeny and taxonomy of Caryophylleae (Caryophyllaceae) Untangling phylogenetic patterns and taxonomic confusion in tribe Caryophylleae (Caryophyllaceae) with special focus on generic boundaries Hossein Madhani,1 Richard Rabeler,2 Atefeh Pirani,3 Bengt Oxelman,4 Guenther Heubl5 & Shahin Zarre1 1 Department of Plant Science, Center of Excellence in Phylogeny of Living Organisms, School of Biology, College of Science, University of Tehran, P.O. Box 14155-6455, Tehran, Iran 2 University of Michigan Herbarium-EEB, 3600 Varsity Drive, Ann Arbor, Michigan 48108-2228, U.S.A. 3 Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, P.O. Box 91775-1436, Mashhad, Iran 4 Department of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530 Göteborg, Sweden 5 Biodiversity Research – Systematic Botany, Department of Biology I, Ludwig-Maximilians-Universität München, Menzinger Str. 67, 80638 München, Germany; and GeoBio Center LMU Author for correspondence: Shahin Zarre, [email protected] DOI https://doi.org/10.12705/671.6 Abstract Assigning correct names to taxa is a challenging goal in the taxonomy of many groups within the Caryophyllaceae. This challenge is most serious in tribe Caryophylleae since the supposed genera seem to be highly artificial, and the available morphological evidence cannot effectively be used for delimitation and exact determination of taxa. The main goal of the present study was to re-assess the monophyly of the genera currently recognized in this tribe using molecular phylogenetic data. We used the sequences of nuclear ribosomal internal transcribed spacer (ITS) and the chloroplast gene rps16 for 135 and 94 accessions, respectively, representing all 16 genera currently recognized in the tribe Caryophylleae, with a rich sampling of Gypsophila as one of the most heterogeneous groups in the tribe. -
Acanthocereus Tetragonus SCORE: 16.0 RATING: High Risk (L.) Hummelinck
TAXON: Acanthocereus tetragonus SCORE: 16.0 RATING: High Risk (L.) Hummelinck Taxon: Acanthocereus tetragonus (L.) Hummelinck Family: Cactaceae Common Name(s): barbed-wire cactus Synonym(s): Acanthocereus occidentalis Britton & Rose chaco Acanthocereus pentagonus (L.) Britton & Rose sword-pear Acanthocereus pitajaya sensu Croizat triangle cactus Cactus pentagonus L. Cactus tetragonus L. Assessor: Chuck Chimera Status: Assessor Approved End Date: 1 Nov 2018 WRA Score: 16.0 Designation: H(HPWRA) Rating: High Risk Keywords: Spiny, Agricultural Weed, Environmental Weed, Dense Thickets, Bird-Dispersed Qsn # Question Answer Option Answer 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? 103 Does the species have weedy races? Species suited to tropical or subtropical climate(s) - If 201 island is primarily wet habitat, then substitute "wet (0-low; 1-intermediate; 2-high) (See Appendix 2) High tropical" for "tropical or subtropical" 202 Quality of climate match data (0-low; 1-intermediate; 2-high) (See Appendix 2) High 203 Broad climate suitability (environmental versatility) y=1, n=0 y Native or naturalized in regions with tropical or 204 y=1, n=0 y subtropical climates Does the species have a history of repeated introductions 205 y=-2, ?=-1, n=0 y outside its natural range? 301 Naturalized beyond native range y = 1*multiplier (see Appendix 2), n= question 205 y 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see Appendix 2) n 303 Agricultural/forestry/horticultural weed n=0, y -
Phylogeny and Biogeography of the Pleistocene Holarctic Steppe and Semi-Desert Goosefoot Plant Krascheninnikovia Ceratoides
Flora 262 (2020) 151504 Contents lists available at ScienceDirect Flora journal homepage: www.elsevier.com/locate/flora Phylogeny and biogeography of the Pleistocene Holarctic steppe and semi- desert goosefoot plant Krascheninnikovia ceratoides T Anna Seidla,*, Ernesto Pérez-Collazosb, Karin Tremetsbergera, Mark Carinec, Pilar Catalánb, Karl-Georg Bernhardta a Institute of Botany, University of Natural Resources and Life Sciences, Gregor-Mendel-Straße 33, 1180 Vienna, Austria b Escuela Politécnica Superior de Huesca, Universidad de Zaragoza, Ctra. Cuarte Km 1, 22071 Huesca, Spain c Natural History Museum, Cromwell Rd, Kensington, London SW7 5BD, UK ARTICLE INFO ABSTRACT Edited by: Chennai Guest Editor Krascheninnikovia ceratoides (Chenopodiaceae) is a steppe and semi-desert plant with two subspecies, K. cer- Keywords: atoides subsp. ceratoides, which is widespread in Eurasia, and K. ceratoides subsp. lanata, which grows in western Altai Mountains and central North America. A few disjunct populations of K. ceratoides subsp. ceratoides are found in Anatolia, Irano-Turanian element Europe and North Africa to the west of its otherwise continuous Eurasian distribution. To understand the evo- rDNA and plastid data lutionary history of this characteristic steppe and semi-desert plant, we analysed its phylogeny and biogeo- phylogeography graphy. We sequenced several loci including ITS, ETS and the chloroplast intergenic spacer regions atpB-rbcL, molecular dating rpl32-trnL and trnL-trnF to establish a time-calibrated phylogeny and reconstruct intraspecific relationships. Pleistocene Furthermore, we identified the ploidy level of individuals. While diploid, tetraploid and hexaploid individuals have been reported in the literature, we were only able to find diploids and tetraploids. The diploids were found in the east of Mongolia, Kazakhstan, Kyrgyzstan, Russia and the USA. -
Karymorphological and Molecular Studies on Seven Species in Polygonoideae (Polygonaceae) in Egypt
Chromosome Botany (2012) 7: 17-22 © Copyright 2012 by the International Society of Chromosome Botany Karymorphological and molecular studies on seven species in Polygonoideae (Polygonaceae) in Egypt Magdy Hussein Abd El-Twab1, Ahmed M. Abdel-Hamid and Hagar Ata A. Mohamed Department of Botany and Microbiology, Faculty of Science, Minia University 61519, El-Minia City, Egypt 1Author for correspondence: ([email protected]) Received January 22, 2012; accepted February 29, 2012 ABSTRACT. Seven species in four genera of the Polygonoideae (Polygonaceae) in Egypt were subjected to karyomorphological and molecular studies in order to identify their chromosomal characteristics and investigate their phylogenetical relationships by the conventional staining method and the 5S rDNA PCR. Seed germination after treatment with low temperature stratifi cation and acidifi cation by concentrated H2SO4 was studied. Three rates of germination were obtained in response to the cold stratifi cation and acidifi cation: 1) High in Polygonum equisetiforme, Persicaria lanigera, Pe. lapathifolia and Pe. salicifolia; 2) low in Rumex dentatus; 3) no effect in R. pictus and Emex spinosa. Variation in the chromosome complements number, length and structure were detected for Po. equisetiforme (2n=58; new count); Pe. lanigera (2n=40; new count); Pe. lapathifolia (2n=22); Pe. salicifolia (2n=60); Emex spinosa (2n=18; a new count); Rumex dentatus (2n=40); and R. pictus (2n=18; a new count). Eighteen polymorphic bands of 5S rDNA were used to determine the similarities among the taxa with the similarity coeffi cient ranging between 0.2 and 0.67. KEYWORDS: Acidifi cation, Chromosomes, 5S rDNA, Polygonaceae, Stratifi cation. The Polygonaceae is cosmopolitic to temperate regions have been widely used to elucidate generic relationships (Täckholm 1974; Boulos 1999). -
Origin and Age of Australian Chenopodiaceae
ARTICLE IN PRESS Organisms, Diversity & Evolution 5 (2005) 59–80 www.elsevier.de/ode Origin and age of Australian Chenopodiaceae Gudrun Kadereita,Ã, DietrichGotzek b, Surrey Jacobsc, Helmut Freitagd aInstitut fu¨r Spezielle Botanik und Botanischer Garten, Johannes Gutenberg-Universita¨t Mainz, D-55099 Mainz, Germany bDepartment of Genetics, University of Georgia, Athens, GA 30602, USA cRoyal Botanic Gardens, Sydney, Australia dArbeitsgruppe Systematik und Morphologie der Pflanzen, Universita¨t Kassel, D-34109 Kassel, Germany Received 20 May 2004; accepted 31 July 2004 Abstract We studied the age, origins, and possible routes of colonization of the Australian Chenopodiaceae. Using a previously published rbcL phylogeny of the Amaranthaceae–Chenopodiaceae alliance (Kadereit et al. 2003) and new ITS phylogenies of the Camphorosmeae and Salicornieae, we conclude that Australia has been reached in at least nine independent colonization events: four in the Chenopodioideae, two in the Salicornieae, and one each in the Camphorosmeae, Suaedeae, and Salsoleae. Where feasible, we used molecular clock estimates to date the ages of the respective lineages. The two oldest lineages both belong to the Chenopodioideae (Scleroblitum and Chenopodium sect. Orthosporum/Dysphania) and date to 42.2–26.0 and 16.1–9.9 Mya, respectively. Most lineages (Australian Camphorosmeae, the Halosarcia lineage in the Salicornieae, Sarcocornia, Chenopodium subg. Chenopodium/Rhagodia, and Atriplex) arrived in Australia during the late Miocene to Pliocene when aridification and increasing salinity changed the landscape of many parts of the continent. The Australian Camphorosmeae and Salicornieae diversified rapidly after their arrival. The molecular-clock results clearly reject the hypothesis of an autochthonous stock of Chenopodiaceae dating back to Gondwanan times. -
CHENOPODIACEAE 藜科 Li Ke Zhu Gelin (朱格麟 Chu Ge-Ling)1; Sergei L
Flora of China 5: 351-414. 2003. CHENOPODIACEAE 藜科 li ke Zhu Gelin (朱格麟 Chu Ge-ling)1; Sergei L. Mosyakin2, Steven E. Clemants3 Herbs annual, subshrubs, or shrubs, rarely perennial herbs or small trees. Stems and branches sometimes jointed (articulate); indumentum of vesicular hairs (furfuraceous or farinose), ramified (dendroid), stellate, rarely of glandular hairs, or plants glabrous. Leaves alternate or opposite, exstipulate, petiolate or sessile; leaf blade flattened, terete, semiterete, or in some species reduced to scales. Flowers monochlamydeous, bisexual or unisexual (plants monoecious or dioecious, rarely polygamous); bracteate or ebracteate. Bractlets (if present) 1 or 2, lanceolate, navicular, or scale-like. Perianth membranous, herbaceous, or succulent, (1–)3–5- parted; segments imbricate, rarely in 2 series, often enlarged and hardened in fruit, or with winged, acicular, or tuberculate appendages abaxially, seldom unmodified (in tribe Atripliceae female flowers without or with poorly developed perianth borne between 2 specialized bracts or at base of a bract). Stamens shorter than or equaling perianth segments and arranged opposite them; filaments subulate or linear, united at base and usually forming a hypogynous disk, sometimes with interstaminal lobes; anthers dorsifixed, incumbent in bud, 2-locular, extrorse, or dehiscent by lateral, longitudinal slits, obtuse or appendaged at apex. Ovary superior, ovoid or globose, of 2–5 carpels, unilocular; ovule 1, campylotropous; style terminal, usually short, with 2(–5) filiform or subulate stigmas, rarely capitate, papillose, or hairy on one side or throughout. Fruit a utricle, rarely a pyxidium (dehiscent capsule); pericarp membranous, leathery, or fleshy, adnate or appressed to seed. Seed horizontal, vertical, or oblique, compressed globose, lenticular, reniform, or obliquely ovoid; testa crustaceous, leathery, membranous, or succulent; embryo annular, semi-annular, or spiral, with narrow cotyledons; endosperm much reduced or absent; perisperm abundant or absent. -
Evolutionary Consequences of Dioecy in Angiosperms: the Effects of Breeding System on Speciation and Extinction Rates
EVOLUTIONARY CONSEQUENCES OF DIOECY IN ANGIOSPERMS: THE EFFECTS OF BREEDING SYSTEM ON SPECIATION AND EXTINCTION RATES by JANA C. HEILBUTH B.Sc, Simon Fraser University, 1996 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in THE FACULTY OF GRADUATE STUDIES (Department of Zoology) We accept this thesis as conforming to the required standard THE UNIVERSITY OF BRITISH COLUMBIA July 2001 © Jana Heilbuth, 2001 Wednesday, April 25, 2001 UBC Special Collections - Thesis Authorisation Form Page: 1 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. The University of British Columbia Vancouver, Canada http://www.library.ubc.ca/spcoll/thesauth.html ABSTRACT Dioecy, the breeding system with male and female function on separate individuals, may affect the ability of a lineage to avoid extinction or speciate. Dioecy is a rare breeding system among the angiosperms (approximately 6% of all flowering plants) while hermaphroditism (having male and female function present within each flower) is predominant. Dioecious angiosperms may be rare because the transitions to dioecy have been recent or because dioecious angiosperms experience decreased diversification rates (speciation minus extinction) compared to plants with other breeding systems. -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings.