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Complete Inventory
Maya Ethnobotany Complete Inventory of plants 1 Fifth edition, November 2011 Maya Ethnobotany Complete Inventory:: fruits,nuts, root crops, grains,construction materials, utilitarian uses, sacred plants, sacred flowers Guatemala, Mexico, Belize, Honduras Nicholas M. Hellmuth Maya Ethnobotany Complete Inventory of plants 2 Introduction This opus is a progress report on over thirty years of studying plants and agriculture of the present-day Maya with the goal of understanding plant usage by the Classic Maya. As a progress report it still has a long way to go before being finished. But even in its unfinished state, this report provides abundant listings of plants in a useful thematic arrangement. The only other publication that I am familiar with which lists even close to most of the plants utilized by the Maya is in an article by Cyrus Lundell (1938). • Obviously books on Mayan agriculture should have informative lists of all Maya agricultural crops, but these do not tend to include plants used for house construction. • There are monumental monographs, such as all the trees of Guatemala (Parker 2008) but they are botanical works, not ethnobotanical, and there is no cross-reference by kind of use. You have to go through over one thousand pages and several thousand tree species to find what you are looking for. • There are even important monographs on Maya ethnobotany, but they are usually limited to one country, or one theme, often medicinal plants. • There are even nice monographs on edible plants of Central America (Chízmar 2009), but these do not include every local edible plant, and their focus is not utilitarian plants at all, nor sacred plants. -
Downloaded from Brill.Com10/07/2021 08:53:11AM Via Free Access 130 IAWA Journal, Vol
IAWA Journal, Vol. 27 (2), 2006: 129–136 WOOD ANATOMY OF CRAIGIA (MALVALES) FROM SOUTHEASTERN YUNNAN, CHINA Steven R. Manchester1, Zhiduan Chen2 and Zhekun Zhou3 SUMMARY Wood anatomy of Craigia W.W. Sm. & W.E. Evans (Malvaceae s.l.), a tree endemic to China and Vietnam, is described in order to provide new characters for assessing its affinities relative to other malvalean genera. Craigia has very low-density wood, with abundant diffuse-in-aggre- gate axial parenchyma and tile cells of the Pterospermum type in the multiseriate rays. Although Craigia is distinct from Tilia by the pres- ence of tile cells, they share the feature of helically thickened vessels – supportive of the sister group status suggested for these two genera by other morphological characters and preliminary molecular data. Although Craigia is well represented in the fossil record based on fruits, we were unable to locate fossil woods corresponding in anatomy to that of the extant genus. Key words: Craigia, Tilia, Malvaceae, wood anatomy, tile cells. INTRODUCTION The genus Craigia is endemic to eastern Asia today, with two species in southern China, one of which also extends into northern Vietnam and southeastern Tibet. The genus was initially placed in Sterculiaceae (Smith & Evans 1921; Hsue 1975), then Tiliaceae (Ren 1989; Ying et al. 1993), and more recently in the broadly circumscribed Malvaceae s.l. (including Sterculiaceae, Tiliaceae, and Bombacaceae) (Judd & Manchester 1997; Alverson et al. 1999; Kubitzki & Bayer 2003). Similarities in pollen morphology and staminodes (Judd & Manchester 1997), and chloroplast gene sequence data (Alverson et al. 1999) have suggested a sister relationship to Tilia. -
Tropical Forests
1740 TROPICAL FORESTS / Bombacaceae in turn cause wild swings in the ecology and these Birks JS and Barnes RD (1990) Provenance Variation in swings themselves can sometimes prove to be beyond Pinus caribaea, P. oocarpa and P. patula ssp. tecunuma- control through management. In the exotic environ- nii. Tropical Forestry Papers no. 21. Oxford, UK: Oxford ments, it is impossible to predict or even conceive of Forestry Institute. the events that may occur and to know their Critchfield WB and Little EL (1966) Geographic Distribu- consequences. Introduction of diversity in the forest tion of the Pines of the World. Washington, DC: USDA Miscellaneous Publications. through mixed ages, mixed species, rotation of Duffield JW (1952) Relationships and species hybridization species, silvicultural treatment, and genetic variation in the genus Pinus. Zeitschrift fu¨r Forstgenetik und may make ecology and management more complex Forstpflanzenzuchtung 1: 93–100. but it will render the crop ecosystem much more Farjon A and Styles BT (1997) Pinus (Pinaceae). Flora stable, robust, and self-perpetuating and provide Neotropica Monograph no. 75. New York: New York buffers against disasters. The forester must treat crop Botanical Garden. protection as part of silvicultural planning. Ivory MH (1980) Ectomycorrhizal fungi of lowland tropical pines in natural forests and exotic plantations. See also: Pathology: Diseases affecting Exotic Planta- In: Mikola P (ed.) Tropical Mycorrhiza Research, tion Species; Diseases of Forest Trees. Temperate and pp. 110–117. Oxford, UK: Oxford University Press. Mediterranean Forests: Northern Coniferous Forests; Ivory MH (1987) Diseases and Disorders of Pines in the Southern Coniferous Forests. Temperate Ecosystems: Tropics. Overseas Research Publication no. -
Biodiversity in Forests of the Ancient Maya Lowlands and Genetic
Biodiversity in Forests of the Ancient Maya Lowlands and Genetic Variation in a Dominant Tree, Manilkara zapota (Sapotaceae): Ecological and Anthropogenic Implications by Kim M. Thompson B.A. Thomas More College M.Ed. University of Cincinnati A Dissertation submitted to the University of Cincinnati, Department of Biological Sciences McMicken College of Arts and Sciences for the degree of Doctor of Philosophy October 25, 2013 Committee Chair: David L. Lentz ABSTRACT The overall goal of this study was to determine if there are associations between silviculture practices of the ancient Maya and the biodiversity of the modern forest. This was accomplished by conducting paleoethnobotanical, ecological and genetic investigations at reforested but historically urbanized ancient Maya ceremonial centers. The first part of our investigation was conducted at Tikal National Park, where we surveyed the tree community of the modern forest and recovered preserved plant remains from ancient Maya archaeological contexts. The second set of investigations focused on genetic variation and structure in Manilkara zapota (L.) P. Royen, one of the dominant trees in both the modern forest and the paleoethnobotanical remains at Tikal. We hypothesized that the dominant trees at Tikal would be positively correlated with the most abundant ancient plant remains recovered from the site and that these trees would have higher economic value for contemporary Maya cultures than trees that were not dominant. We identified 124 species of trees and vines in 43 families. Moderate levels of evenness (J=0.69-0.80) were observed among tree species with shared levels of dominance (1-D=0.94). From the paleoethnobotanical remains, we identified a total of 77 morphospecies of woods representing at least 31 plant families with 38 identified to the species level. -
Appendix 1 Vernacular Names
Appendix 1 Vernacular Names The vernacular names listed below have been collected from the literature. Few have phonetic spellings. Spelling is not helped by the difficulties of transcribing unwritten languages into European syllables and Roman script. Some languages have several names for the same species. Further complications arise from the various dialects and corruptions within a language, and use of names borrowed from other languages. Where the people are bilingual the person recording the name may fail to check which language it comes from. For example, in northern Sahel where Arabic is the lingua franca, the recorded names, supposedly Arabic, include a number from local languages. Sometimes the same name may be used for several species. For example, kiri is the Susu name for both Adansonia digitata and Drypetes afzelii. There is nothing unusual about such complications. For example, Grigson (1955) cites 52 English synonyms for the common dandelion (Taraxacum officinale) in the British Isles, and also mentions several examples of the same vernacular name applying to different species. Even Theophrastus in c. 300 BC complained that there were three plants called strykhnos, which were edible, soporific or hallucinogenic (Hort 1916). Languages and history are linked and it is hoped that understanding how lan- guages spread will lead to the discovery of the historical origins of some of the vernacular names for the baobab. The classification followed here is that of Gordon (2005) updated and edited by Blench (2005, personal communication). Alternative family names are shown in square brackets, dialects in parenthesis. Superscript Arabic numbers refer to references to the vernacular names; Roman numbers refer to further information in Section 4. -
Grijalva Pineda, Alfredo. Flora Útil Etnobotánica De Nicaragua
FLORA ÚTIL ETNOBOTÁNICA DE NICARAGUA. Alfredo Grijalva Pineda. Managua, Nicaragua; Junio del 2006 N 581 G857 Grijalva Pineda, Alfredo Flora útil etnobotánica de Nicaragua / Alfredo Grijalva Pineda. --1a ed.-- Managua : MARENA, 2005. 290 p. : il. ISBN : 99924-903-8-1 1. PLANTAS ÚTILES-INVESTIGACIONES. 2 PLANTAS MEDICINALES 3. TAXONOMÍA VEGETAL Primera edición, 2006, financiada con fondos de la Agencia Española de Cooperación Internacional - AECI, en el marco del Proyecto Integral MARENA/ARAUCARIA Río San Juan, ejecutado por el Gobierno de la República de Nicaragua, a través del Ministerio del Ambiente y los Recursos Naturales - MARENA. Teléfono/Fax: 26391271/ 2331595 Fotografías de portada: Bambusa vulgaris, Melicoccus bijugatus, Gerbera jamesonii, Oxalis debilis (Fotografías de Alfredo Grijalva Pineda). Diseño y Diagramación: Franklin Ruíz M. Esta primera edición cuenta de 500 ejemplares, se terminó de imprimir el 26 de junio del 2006. © MARENA – ARAUCARIA – AECI, 2006 © Grijalva Pineda Alfredo Flora Útil Etnobotánica de Nicaragua Presentación Nicaragua es un país megadiverso, que conserva una gran cantidad de ecosistemas y especies de plantas vasculares de gran valor etnobotánico. Concretamente, éste valor se centra en el conocimiento popular sobre la vegetación y sus usos tradicionales o sea de la relación sociedad – planta, la cual hoy en día se vuelve mas importante, dinámica y necesaria para satisfacer muchas necesidades en el campo y la ciudad, tanto en el ámbito alimenticio, medicinal, industrial, ornamental, habitacional, sumidero de la contaminación del aire, entre otras. El objeto de éste libro titulado “Flora Útil o Etnobotánica”, radica en brindar la información y los conocimientos técnicos - científicos a los investigadores, docentes, estudiantes, ambientalistas y personas interesadas en la protección de la biodiversidad, especialmente las plantas de interés económico para la sociedad, así como, el conocimiento de la vegetación y sus propiedades. -
11. NOVEDADES TAXONÓMICAS Y COROLÓGICAS EN MATISIA Y QUARARIBEA DEL NORTE DE SUDAMÉRICA
Caldasia 23(2): 351-382 BOMBACACEAE NEOTROPICAE NOVAE VEL MINUS COGNITAE - 11. NOVEDADES TAXONÓMICAS Y COROLÓGICAS EN MATISIA y QUARARIBEA DEL NORTE DE SUDAMÉRICA JOSÉ LUIS FERNÁNDEZ-ALONSO Instituto de Ciencias Naturales, Universidad Nacional de Colombia, Apartado 7495, Bogo- tá, Colombia. [email protected] RESUMEN Como parte de los trabajos que actualmente se adelantan en la tribu Quararibeae (Bombacaceae) en el norte de Sudamérica, se describen 5 especies nuevas y una subespecie del género Matisia Humb. & Bonpl. (M a/ata Little subsp. corrugata, M carderi, M hirsutissima, M lozanoi, M serpicostata y M spathacea) y dos especies de Quararibea Aubl. (Q. cogol!oi y Q. tulekunae). Asimismo, se aclaran aspectos taxonómicos o se registran novedades coro lógicas para Colombia, Ecua- dor o Perú, referentes a las especies Malata Little, M cornucopiae Triana & Planch., M jloccosa Fern.-Alonso, M giacomettoi Romero, M hirta Cuatrec., M leptandra Cuatrec., M soegengii Cuatrec., Quararibea ciroana Cuatrec. y Q. wittii Ulbr. Palabras clave. Bombacaceae, Corología, Colombia, Ecuador, Matisia, Neotrópico, Perú, Quararibea, Quararibeae, Taxonomía. A BSTRACT As part ofthe work in progress in the tribe Quararibeae (Bombacaceae) from northern South America, five new species and one subspecies of Matisia Humb. & Bonp\. and two species of Quararibea Aubl. are described (M alata Little subsp. corrugata, M carderi, M hirsutissima, M lozanoi, M. serpicostata, M. spathacea, Quararibea cogol!oi and Q. tulekunae). Also, some taxonomic aspects are discussed and sorne chorologic novelties from Colombia, Ecuador and Perú are registered, in the following species: Malata Little subsp. alata, M cornucopiae Triana & Planch., Mjloccosa Fern.Alonso, M giacomettoi Romero, M hirta Cuatrec., M leptandra Cuatrec., M soegengii Cuatrec., Quararibea ciroana Cuatrec., and Q. -
UNIVERSITY of CALIFORNIA RIVERSIDE Systematics And
UNIVERSITY OF CALIFORNIA RIVERSIDE Systematics and Ethnobotany of Salvia Subgenus Calosphace and Origins of the Hallucinogenic Sage, Salvia divinorum A Dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Plant Biology by Aaron Allon Jenks March 2009 Dissertation Committee: Dr. Seung-Chul Kim, Chairperson Dr. J. Giles Waines Dr. J. Travis Columbus Copyright by Aaron Allon Jenks 2009 The Dissertation of Aaron Allon Jenks is approved: _________________________________________ _________________________________________ _________________________________________ Committee Chairperson University of California, Riverside ACKNOWLEDGEMENTS A number of individuals and organizations are deserving of thanks and acknowledgement for their contributions, both personal and professional, to the completion of this project. Most of all I would like to thank my wonderful wife, Allison Bacon, for her love and support throughout my years at UC Riverside. She admirably and amiably tolerated our house and yard becoming overgrown with multitudes of sages and a husband obsessed with plants. I love you above all else, Allison. I am also extremely thankful for the newest member of my family, our son Aidan Avery Jenks, who was born during my graduate stint at UCR. With his bright life and joyous inquisitiveness, he has blessed our lives immeasurably. I also thank my parents, Larry and Betty Jenks, for their constant love and their unflagging belief that I could accomplish whatever I set my mind toward. ‘Twas their intruduction to natural world via weekend campouts in the mountains and horse pack-trips into the Wallowas of Eastern Oregon, that early instilled in me a wonder and love of Nature. A number of individuals have directly contributed to the completion of my dissertation. -
A New Species of Quararibea (Malvaceae) from Costa Rica
Zamora, N.A., A. Cascante-Marín, S. Choi, y S.-Y. Kim. 2017. A new species of Quararibea (Malvaceae) from Costa Rica. Phytoneuron 2017-67: 1–6. Published 27 September 2017. ISSN 2153 733X A NEW SPECIES OF QUARARIBEA (MALVACEAE) FROM COSTA RICA NELSON A. ZAMORA Herbario Nacional de Costa Rica (CR) Departamento de Historia Natural, Museo Nacional de Costa Rica Apdo. 749-1000, San José, Costa Rica [email protected] ALFREDO CASCANTE -MARÍN Escuela de Biología y Herbario USJ Universidad de Costa Rica Sede Rodrigo Facio, Código Postal 11501-2060 San Pedro de Montes de Oca, San José, Costa Rica [email protected] SANGHO CHOI International Biological Material Research Center Korea Research Institute of Bioscience and Biotechnology P. O. Box 34141, Daejeon, South Korea [email protected] SOO -YONG KIM International Biological Material Research Center Korea Research Institute of Bioscience and Biotechnology P. O. Box 34141, Daejeon, South Korea [email protected] ABSTRACT Some previous collections of Quararibea nigrescens have been misidentified, confused or tentatively assigned to Quararibea costaricensis . Both species, however, can be consistently distinguished because Q. nigrescens has always twigs, leaves and calyx conspicuously silvery or grayish lepidote or stellate-peltate pubescent , while in Q. costaricensis twigs and leaves are sparsely diminute tomentulose with dark brown fasciculate or rufous-brown stellate or stellate-peltate pubescent, becoming essentially glabrate with age, except, the calyx which possesses a dense pubescence of granuliferous-lepidote golden or greenish-brown trichomes. The proposed species name, Q. nigrescens , refers to the peculiar, unique and consistent dark gray, blackish to almost black color of leaves (mainly) that is noticeable upon drying, while in Q. -
Host-Generalist Fungal Pathogens of Seedlings May Maintain Forest
1 Supporting Information 2 Article title: : Host-generalist fungal pathogens of seedlings may maintain forest diversity via 3 host-specific impacts and differential susceptibility among tree species 4 Authors: Erin R. Spear and Kirk D. Broders 5 6 The following Supporting Information is available for this article: 7 Fig. S1 Examples of disease symptoms in the forests of Panama. 8 Fig. S2 Details of shadehouse-based inoculation experiments. 9 Fig. S3 Rank abundance plot and OTU accumulation curve. 10 Fig. S4 Overlap in fungal OTUs among sampling years, methods used to obtain symptomatic 11 seedlings, isolation media, and tissue sampled. 12 Fig. S5 Correlation between OTU host range and isolation frequency. 13 Table S1 Taxonomic assignments, traits, sampling effort, and observed OTUs for tree species 14 evaluated in our survey and experimental approaches. 15 Table S2 Methodological details pertaining to the multi-year collection of symptomatic 16 seedlings, and microbial isolation and sequencing. 17 Table S3 Average light levels, air temperatures, and relative humidities of the shadehouses 18 used for inoculation experiments versus ambient conditions. 19 Table S4 Estimated taxonomic placement, isolation frequency, number of observed hosts, 20 estimated host specialization, and phylogenetic pattern of host use of the OTUs. 21 Table S5 Overlap in seedling-associated OTUs among tree species. 22 Table S6 Results of the beta-binomial generalized linear regression with the proportion of 23 diseased seedlings as a function of seed size and shade tolerance. 24 Table S7 Average estimates based on the best-ranked beta-binomial generalized linear 1 25 regressions with the proportion of diseased seedlings as a function of seed size and spatial 26 distribution relative to annual rainfall. -
Fruit Trees and Useful Plants in Amazonian Life (2011)
FAO TECHNICAL PAPERS NON-WOOD FOREST PRODUCTS 1. Flavours and fragrances of plant origin (1995) 2. Gum naval stores: turpentine and rosin from pine resin (1995) 3. Report of the International Expert Consultation on Non-Wood Forest Products (1995) 4. Natural colourants and dyestuffs (1995) 5. Edible nuts (1995) 6. Gums, resins and latexes of plant origin (1995) 7. Non-wood forest products for rural income and sustainable forestry (1995) 8. Trade restrictions affecting international trade in non-wood forest products (1995) 9. Domestication and commercialization of non-timber forest products in agroforestry systems (1996) 10. Tropical palms (1998) 11. Medicinal plants for forest conservation and health care (1997) 12. Non-wood forest products from conifers (1998) 13. Resource assessment of non-wood forest products Experience and biometric principles (2001) 14. Rattan – Current research issues and prospects for conservation and sustainable development (2002) 15. Non-wood forest products from temperate broad-leaved trees (2002) 16. Rattan glossary and Compendium glossary with emphasis on Africa (2004) 17. Wild edible fungi – A global overview of their use and importance to people (2004) 18. World bamboo resources – A thematic study prepared in the framework of the Global Forest Resources Assessment 2005 (2007) 19. Bees and their role in forest livelihoods – A guide to the services provided by bees and the sustainable harvesting, processing and marketing of their products (2009) 20. Fruit trees and useful plants in Amazonian life (2011) The -
Appendix A: Ethnic Names of Stingless Bees
Appendix A: Ethnic Names of Stingless Bees “abeja amarilla” Oxytrigona mellicolor “abejita negra” Scaura sp. aff. longula Ecuador, 216, Ecuador, 216 “abeja amarilla” Partamona aequatoriana “abejita negra” Trigona cf. branneri Ecuador, 216 Ecuador, 217 “abeja amarilla” Trigona cf. amazonensis “abejita suca” Nannotrigona melanocera Ecuador, 217 Ecuador, 216 “abeja amarilla” Trigona dallatorreana “ajavitte” Tetragona clavipes Venezuela, 427 Ecuador, 217 “alpargate” Plebeia sp Ecuador, 423 “abeja amarilla” Trigona ferricauda “angelina” Nannotrigona melanocera Ecuador, 217 Ecuador, 216 “abeja ángel” Tetragonisca angustula “angelina” Tetragonisca angustula Ecuador, 217 Ecuador, 216 “angelita” Tetragonisca angustula Ecuador, “abeja chiquita” Paratrigona cf. rinconi Venezuela, 221, 340, 423 Ecuador, 216 “angelita” Frieseomelitta aff. varia “abeja de tierra” Geotrigona sp. Ecuador, 423 Venezuela, 364 “abeja de tierra” Trigona fulviventris Ecuador, “angelita negra” Aparatrigona impunctata 217, 423 Ecuador, 216 “abeja del suelo” Schwarziana quadripunctata “angelita negra grande” Trigona cf. guianae Argentina, 290, 294 Ecuador, 217 “abeja finita” Tetragonisca angustula “abejita negra” Nannotrigona melanocera Ecuador, 216 Ecuador, 216 “abeja negra” Paratrigona cf. rinconi “arapuá” Trigona spinipes Brazil, 439 Ecuador, 216 “arepe” Nannotrigona sp Ecuador, 423 “abeja negra” Partamona aequatoriana “auim” Trigona amazonensis Ecuador, 204 Ecuador, 216 “auímo”Melipona crinita Ecuador, 204 “abeja negra” Trigona sp. gr. fuscipennis “auñeta”Partamona epiphytophila