Asteraceae) in Mexico
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Sistema De Clasificación Artificial De Las Magnoliatas Sinántropas De Cuba
Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA Pedro- Pabfc He.r retira Qltver CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver PROGRAMA DE DOCTORADO COOPERADO DESARROLLO SOSTENIBLE: MANEJOS FORESTAL Y TURÍSTICO UNIVERSIDAD DE ALICANTE, ESPAÑA Y UNIVERSIDAD DE PINAR DEL RÍO, CUBA TESIS EN OPCIÓN AL GRADO CIENTÍFICO DE DOCTOR EN CIENCIAS SISTEMA DE CLASIFICACIÓN ARTIFICIAL DE LAS MAGNOLIATAS SINÁNTROPAS DE CUBA ASPIRANTE: Lie. Pedro Pablo Herrera Oliver Investigador Auxiliar Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente DIRECTORES: CUBA Dra. Nancy Esther Ricardo Ñapóles Investigador Titular Centro Nacional de Biodiversidad Instituto de Ecología y Sistemática Ministerio de Ciencias, Tecnología y Medio Ambiente ESPAÑA Dr. Andreu Bonet Jornet Piiofesjar Titular Departamento de EGdfegfe Universidad! dte Mearte CUBA 2006 Tesis doctoral de la Univerisdad de Alicante. Tesi doctoral de la Universitat d'Alacant. 2007 Sistema de clasificación artificial de las magnoliatas sinántropas de Cuba. Pedro Pablo Herrera Oliver I. INTRODUCCIÓN 1 II. ANTECEDENTES 6 2.1 Historia de los esquemas de clasificación de las especies sinántropas (1903-2005) 6 2.2 Historia del conocimiento de las plantas sinantrópicas en Cuba 14 III. -
California Indian Garden – Plant List and Plant Uses
California Indian Garden Plant List Spring 2018 Common name Scientific name Indian Uses Bladderpod Isomeris arborea Seeds and flowers eaten Black sage Salvia mellifera Seeds ground into a meal for baking; tea made from leaves and stem Blue elderberry Sambucus nigra Berries used as food and sauce, plant also used for medicine, dyes for basketry, arrow shafts, flute, whistles, clapper sticks, and folk medicine Bush monkey flower Mimulus aurantiacus Young stems and leaves eaten as greens; used to treat burns, wounds, colds, cough, flu, stomach disorders and heart ailments CA buckwheat Eriogonum fasciculatum Leaf tea used for headache and stomach pain, root tea for colds and laryngitis; root poultice applied to wounds Chamise Adenostoma fasciculatum Infusion of bark and leaves used to cure syphilis; oils used to treat skin infections; scale insect on plant used as a binding agent; branches used to make arrow shafts and points Coast cholla Cylindropuntia prolifera Flowers and fruits for food Coast live oak Quercus agrifolia Acorns used as an important food staple Coast prickly pear Opuntia littoralis Fruit used for food, syrup, juice, candy and gum; young, green nopales (stems) also eaten; used to treat wounds, rheumatism, mumps, and reduce swelling; spines for needles and juice for dye Coast sunflower Encelia californica No known uses Coastal sagebrush Artemisia californica Leaves used for a variety of medicinal treatments: toothaches, wounds, asthma, colds, coughs, rheumatism, menstrual problems, to ease childbirth, menopausal symptoms, -
The Santa Margarita River Arundo Donax Control Project: Development of Methods and Plant Community Response1
The Santa Margarita River Arundo donax Control Project: Development of Methods and Plant Community Response1 Dawn M. Lawson2, Jesse A. Giessow, and Jason H. Giessow3 Abstract A large-scale effort to control the aggressively invasive exotic species Arundo donax in the Santa Margarita River watershed in California’s south coast ecoregion was initiated in 1997. The project was prompted by the need for Marine Corps Base Camp Pendleton to address impacts to habitat for federally-listed endangered species and wetlands regulated by the Army Corps of Engineers. As of 2000, 27 km of the main stem of the Santa Margarita River had been treated. The methods employed were tested in preliminary trials before widespread implementation; additional techniques emerged during the course of the project. Although the primary target is A. donax, 14 other invasive exotic species that also threaten riparian ecosystem functions were treated when encountered. Vegetation-monitoring transects were established in A. donax removal areas to document the effectiveness of the different treatments and recovery of plant communities. A. donax was reduced by over 90 percent after the first treatment and accounted for less than 2 percent absolute cover after three follow-up annual treatments. An experiment testing low-cost methods for establishing woody species after A. donax control was also conducted. Cuttings were installed with no follow-up maintenance. Approximately 30 percent of Baccharis salicifolia and large (3-6 m) willow cuttings survived 2 years. Key words: Arundo donax control, invasive species, riparian restoration, Santa Margarita River Introduction Arundo donax is an invasive, non-native plant seriously impacting much of the riparian habitat throughout coastal California including Marine Corps Base Camp Pendleton. -
Baccharis Salicifolia
Baccharis salicifolia (Mulefat) Leaf: Alternate, simple, evergreen, lanceolate, 3 to 5 inches long, widely spaced fine teeth, maybe sticky, shiny green above, paler below. Flower: Dioecious; white, 1/2 inch across, displayed in open terminal flower heads or tighter clusters from axils, appear nearly year round. Fruit: A small achene tipped with long feathery white bristles (dandelion like), often in great abundance. Twig: Very pithy, light brown to golden brown, sticky green when young. Leaf scars are narrow and raised. Bark: Grayish brown shallowly ridged with reddish furrows. Form: An up to 8 foot tall, suckering, thicket forming shrub, generally graceful. Populus fremontii (Fremont Cottonwood) Leaf: Alternate, simple, broadly cordate to triangular, coarsely crenate, 2 to 4 inches long, petiole flattened, shiny green above, sometimes pubescent beneath. Flower: Dioecious; males and females as hanging catkins, 2 to 4 inches long, yellow-green, appearing in early spring before the leaves. Fruit: Light brown, small egg-shaped capsules, splits (3 parts) to disseminate numerous, small cottony seeds. Twig: Moderate to stout, gray-brown to yellow-brown, swollen at leaf scars; large green-brown pointed bud, not sticky; twig has a bitter aspirin taste. Bark: Light gray-brown, becoming deeply furrowed with flat-topped ridges. Form: Reaches up to 60 feet in height with a broad, flat-topped crown, with a trunk up to 2 to 3 feet in diameter. Salix lasiolepis (Arroyo Willow) Leaf: Alternate, simple, lanceolate to narrowly obovate, 3 to 6 inches long, margins wavy or with a few wavy teeth, thick and somewhat leathery, shiny dark green above, whitish beneath. -
Reference Plant List
APPENDIX J NATIVE & INVASIVE PLANT LIST The following tables capture the referenced plants, native and invasive species, found throughout this document. The Wildlife Action Plan Team elected to only use common names for plants to improve the readability, particular for the general reader. However, common names can create confusion for a variety of reasons. Common names can change from region-to-region; one common name can refer to more than one species; and common names have a way of changing over time. For example, there are two widespread species of greasewood in Nevada, and numerous species of sagebrush. In everyday conversation generic common names usually work well. But if you are considering management activities, landscape restoration or the habitat needs of a particular wildlife species, the need to differentiate between plant species and even subspecies suddenly takes on critical importance. This appendix provides the reader with a cross reference between the common plant names used in this document’s text, and the scientific names that link common names to the precise species to which writers referenced. With regards to invasive plants, all species listed under the Nevada Revised Statute 555 (NRS 555) as a “Noxious Weed” will be notated, within the larger table, as such. A noxious weed is a plant that has been designated by the state as a “species of plant which is, or is likely to be, detrimental or destructive and difficult to control or eradicate” (NRS 555.05). To assist the reader, we also included a separate table detailing the noxious weeds, category level (A, B, or C), and the typical habitats that these species invade. -
Flora-Lab-Manual.Pdf
LabLab MManualanual ttoo tthehe Jane Mygatt Juliana Medeiros Flora of New Mexico Lab Manual to the Flora of New Mexico Jane Mygatt Juliana Medeiros University of New Mexico Herbarium Museum of Southwestern Biology MSC03 2020 1 University of New Mexico Albuquerque, NM, USA 87131-0001 October 2009 Contents page Introduction VI Acknowledgments VI Seed Plant Phylogeny 1 Timeline for the Evolution of Seed Plants 2 Non-fl owering Seed Plants 3 Order Gnetales Ephedraceae 4 Order (ungrouped) The Conifers Cupressaceae 5 Pinaceae 8 Field Trips 13 Sandia Crest 14 Las Huertas Canyon 20 Sevilleta 24 West Mesa 30 Rio Grande Bosque 34 Flowering Seed Plants- The Monocots 40 Order Alistmatales Lemnaceae 41 Order Asparagales Iridaceae 42 Orchidaceae 43 Order Commelinales Commelinaceae 45 Order Liliales Liliaceae 46 Order Poales Cyperaceae 47 Juncaceae 49 Poaceae 50 Typhaceae 53 Flowering Seed Plants- The Eudicots 54 Order (ungrouped) Nymphaeaceae 55 Order Proteales Platanaceae 56 Order Ranunculales Berberidaceae 57 Papaveraceae 58 Ranunculaceae 59 III page Core Eudicots 61 Saxifragales Crassulaceae 62 Saxifragaceae 63 Rosids Order Zygophyllales Zygophyllaceae 64 Rosid I Order Cucurbitales Cucurbitaceae 65 Order Fabales Fabaceae 66 Order Fagales Betulaceae 69 Fagaceae 70 Juglandaceae 71 Order Malpighiales Euphorbiaceae 72 Linaceae 73 Salicaceae 74 Violaceae 75 Order Rosales Elaeagnaceae 76 Rosaceae 77 Ulmaceae 81 Rosid II Order Brassicales Brassicaceae 82 Capparaceae 84 Order Geraniales Geraniaceae 85 Order Malvales Malvaceae 86 Order Myrtales Onagraceae -
LESQ Profile for Postingv2.Xlsx
I. SPECIES Lepidospartum squamatum (A. Gray) A. Gray NRCS CODE: Family: Asteraceae LESQ Order: Asterales Tribe: Senecioneae Class: Magnoliopsida Scale leaves (top); mature plant in early April before active growth resumed (bottom); flowering plant and plant in fruit in fall (right). (photos, A. Montalvo) Discoid head (top). Whitish pappus of ripe achenes (bottom). A. Subspecific taxa None currently recognized (Jepson eFlora 2016, FNA 2016). B. Synonyms L. squamatum var. palmeri (A. Gray) A. Gray L. C. Wheeler. (FNA 2016) L. squamatum (A. Gray) A. Gray var. obtectum Jeps. (Munz & Keck 1968, Munz 1974) Linosyris squamata A. Gray Tetradymia s. A. Gray (Munz 1974) Baccharis sarothroides A. Gray var. pluricephala Jeps. (JepsonOnline) C. Common name Scalebroom; also scale-broom, California broomsage, broomscale (Calflora 2016, Painter 2016) D. Taxonomic relationships Phylogenetic work shows Lepidospartum is most closely allied with Tetradymia (Pelser et al. 2007). There are three species of Lepidospartum in North America (FNA 2016). Lepidospartum latisquamum S. Watson occurs in desert washes and fans in eastern California, Utah, and Nevada from about 3,000 to 8,200 ft (915 to 2,500 m). L. burgessii B. L. Turner is a rare taxon associated with gypsum soils in desert basins of New Mexico, Texas, and Mexico. E. Related taxa in region L. latisquamum potentially overlaps in distribution with L. squamatum in the Mojave Desert region and lower edges of the San Gabriel Mountains from the Cajon Pass area northward. It differs from L. squamatum in having fewer (only 4–6) flowers per head, corollas extending well beyond the involucre, tomentose phyllaries, and much longer, thread or needle like leaves (20–30 mm). -
Asteraceae): a Review of Their Antimicrobial Activity
Vol. 11(3), pp. 43-57, 17 January, 2017 DOI: 10.5897/JMPR2016.6313 Article Number: 4F30B6962396 ISSN 1996-0875 Journal of Medicinal Plants Research Copyright © 2017 Author(s) retain the copyright of this article http://www.academicjournals.org/JMPR Review The genus Eupatorium L. (Asteraceae): A review of their antimicrobial activity Antonio Carlos Nogueira Sobrinho1*, Selene Maia de Morais1, Elnatan Bezerra de Souza2 and Raquel Oliveira dos Santos Fontenelle2 1Postgraduate Program in Biotechnology-Renorbio, Center for Science and Technology, State University of Ceará, Fortaleza, Brazil. 2Course of Biological Sciences, Center for Agricultural Sciences and Biological Sciences, State University of Vale do Acaraú, Sobral, Brazil. Received 30 November, 2016; Accepted 6 January, 2017 In recent years, the number of infectious diseases linked to the occurrence of bacterial and fungal resistance has increased, leading to extensive search for new drugs to treat these infections. Species of the Asteraceae family and the genus Eupatorium, have high biological potential and are used in folk medicine to treat various diseases. This review article presents the main phytochemical and biological characteristics of the Asteraceae family and the genus Eupatorium s.l., whose antimicrobial activity is promising, especially antibacterial and antifungal activity. The current review was achieved using an organized search of the scientific data published on antimicrobial activity and phytochemical of the species of the genus Eupatorium using various databases, including PubMed, ScienceDirect, Scopus, Scielo, SciFinder and Google Scholar. The species of Eupatorium are rich in terpenes, phytosterols and sesquiterpene lactones, the latter being chemotaxonomic markers of the group, with broad anticancer, antiplasmodial and antimicrobial activity, making them promising for the development of new drugs. -
Complete List of Literature Cited* Compiled by Franz Stadler
AppendixE Complete list of literature cited* Compiled by Franz Stadler Aa, A.J. van der 1859. Francq Van Berkhey (Johanes Le). Pp. Proceedings of the National Academy of Sciences of the United States 194–201 in: Biographisch Woordenboek der Nederlanden, vol. 6. of America 100: 4649–4654. Van Brederode, Haarlem. Adams, K.L. & Wendel, J.F. 2005. Polyploidy and genome Abdel Aal, M., Bohlmann, F., Sarg, T., El-Domiaty, M. & evolution in plants. Current Opinion in Plant Biology 8: 135– Nordenstam, B. 1988. Oplopane derivatives from Acrisione 141. denticulata. Phytochemistry 27: 2599–2602. Adanson, M. 1757. Histoire naturelle du Sénégal. Bauche, Paris. Abegaz, B.M., Keige, A.W., Diaz, J.D. & Herz, W. 1994. Adanson, M. 1763. Familles des Plantes. Vincent, Paris. Sesquiterpene lactones and other constituents of Vernonia spe- Adeboye, O.D., Ajayi, S.A., Baidu-Forson, J.J. & Opabode, cies from Ethiopia. Phytochemistry 37: 191–196. J.T. 2005. Seed constraint to cultivation and productivity of Abosi, A.O. & Raseroka, B.H. 2003. In vivo antimalarial ac- African indigenous leaf vegetables. African Journal of Bio tech- tivity of Vernonia amygdalina. British Journal of Biomedical Science nology 4: 1480–1484. 60: 89–91. Adylov, T.A. & Zuckerwanik, T.I. (eds.). 1993. Opredelitel Abrahamson, W.G., Blair, C.P., Eubanks, M.D. & More- rasteniy Srednei Azii, vol. 10. Conspectus fl orae Asiae Mediae, vol. head, S.A. 2003. Sequential radiation of unrelated organ- 10. Isdatelstvo Fan Respubliki Uzbekistan, Tashkent. isms: the gall fl y Eurosta solidaginis and the tumbling fl ower Afolayan, A.J. 2003. Extracts from the shoots of Arctotis arcto- beetle Mordellistena convicta. -
Chemical Profile of the Volatiles of Baccharis Salicifolia (Asteraceae)
Acta Agronómica (2019) 68 (3) p 222-227 ISSN 0120-2812 | e-ISSN 2323-0118 doi: https://doi.org/10.15446/acag.v68n3.71063 Chemical profile of the volatiles of Baccharis salicifolia (Asteraceae) and interaction with Macrodactylus nigripes (Coleoptera: Melolonthidae) Perfil químico de volátiles de Baccharis salicifolia (Asteraceae) e interacción con Macrodactylus nigripes (Coleoptera:Melolonthidae) Ericka Nieves-Silva1* and Angel A. Romero-López2 1 Benemérita Universidad Autónoma de Puebla, Centro de Agroecología, Laboratorio de Manejo de Plagas y Enfermedades, Edificio VAL1, Km 1.7 carretera a San Baltazar Tetela, San Pedro Zacachimalpa, C.P. 72960, Puebla, Puebla, México. 2 Benemérita Universidad Autónoma de Puebla, Facultad de Ciencias Biológicas, Laboratorio de Infoquímicos, Blvd. Valsequillo y Av. San Claudio Edificio 112-A, Ciudad universitaria, Col. Jardines de San Manuel, C.P. 72570. Puebla, Puebla, México. *Corresponding autor:[email protected] Rec.:2018-03-16 Acept.: 2019-08-10 Abstract Plant products or substances mediate interactions among organisms from different trophic levels, including phytophagous insects. These interactions have been cited in a chemical-ecology context for species of Coleoptera Melolonthidae. However, there are no previous reports of these interactions among melolonthid beetles species distributed in Mexico and host plants. For the above, the interaction between adults of ‘rose chafer’ Macrodactylus nigripes Bates (Coleoptera:Melolonthidae) and ‘seep willow’ shrub Baccharis salicifolia (Ruíz and Pav.) Pers. (Asteraceae) was recorded and the leaves volatiles of seep willow that might be involved in the attraction of these insects were extracted and identified. The sequence of behavior patterns that conforms this interaction was described. Females of M. nigripes emerge from the soil and flight to the leaves of seep willow shrubs. -
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Redalyc.Chemical Composition and Evaluation of Antibacterial Activity Of
Boletín Latinoamericano y del Caribe de Plantas Medicinales y Aromáticas ISSN: 0717-7917 [email protected] Universidad de Santiago de Chile Chile TORRES-BARAJAS, Lizzeth; ROJAS-VERA, Janne; MORALES-MÉNDEZ, Antonio; ROJAS-FERMÍN, Luís; LUCENA, María; BUITRAGO, Alexis Chemical composition and evaluation of antibacterial activity of essential oils of Ageratina jahnii and Ageratina pichinchensis collected in Mérida, Venezuela Boletín Latinoamericano y del Caribe de Plantas Medicinales y Aromáticas, vol. 12, núm. 1, enero, 2013, pp. 92-98 Universidad de Santiago de Chile Santiago, Chile Available in: http://www.redalyc.org/articulo.oa?id=85625709010 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative © 2013 Boletín Latinoamericano y del Caribe de Plantas Medicinales y Aromáticas 12 (1): 92 - 98 ISSN 0717 7917 www.blacpma.usach.cl Artículo Original | Original Article Chemical composition and evaluation of antibacterial activity of essential oils of Ageratina jahnii and Ageratina pichinchensis collected in Mérida, Venezuela [Composición química y evaluación de la actividad antibacteriana de los aceites esenciales de Ageratina jahnii y Ageratina pichinchensis recolectadas en Mérida,Venezuela] Lizzeth TORRES-BARAJAS1, Janne ROJAS-VERA*1, Antonio MORALES-MÉNDEZ1, Luís ROJAS-FERMÍN1, María LUCENA2 & Alexis BUITRAGO1 1Organic Biomolecular Research Group, Research Institute, Faculty of Pharmacy and Biomedical Sciences. University of Los Andes. Mérida, Venezuela. 2Clinical Bioanalysis Department, Faculty of Pharmacy and Bioanalysis, University of Los Andes, Mérida, Venezuela Contactos | Contacts: Janne ROJAS VERA - E-mail address: [email protected] Abstract Essential oil from leaves of Ageratina jahnii (B.L.Rob.) R.