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Review Article Ficus Carica L. (Moraceae): Phytochemistry, Traditional Uses and Biological Activities
Hindawi Publishing Corporation Evidence-Based Complementary and Alternative Medicine Volume 2013, Article ID 974256, 8 pages http://dx.doi.org/10.1155/2013/974256 Review Article Ficus carica L. (Moraceae): Phytochemistry, Traditional Uses and Biological Activities Shukranul Mawa, Khairana Husain, and Ibrahim Jantan Drug and Herbal Research Centre, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, JalanRajaMudaAbdulAziz,50300KualaLumpur,Malaysia Correspondence should be addressed to Khairana Husain; [email protected] Received 10 June 2013; Accepted 13 August 2013 Academic Editor: Angelo Antonio Izzo Copyright © 2013 Shukranul Mawa 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. This paper describes the botanical features of Ficus carica L. (Moraceae), its wide variety of chemical constituents, its use in traditional medicine as remedies for many health problems, and its biological activities. The plant has been used traditionally to treat various ailments such as gastric problems, inflammation, and cancer. Phytochemical studies on the leaves and fruits of the plant have shown that they are rich in phenolics, organic acids, and volatile compounds. However, there is little information on the phytochemicals present in the stem and root. Reports on the biological activities of the plant are mainly on its crude extracts which have been proven to possess many biological activities. Some of the most interesting therapeutic effects include anticancer, hepatoprotective, hypoglycemic, hypolipidemic, and antimicrobial activities. Thus, studies related to identification of the bioactive compounds and correlating them to their biological activities are very useful for further research to explore the potential of F. -
Phenology of Ficus Variegata in a Seasonal Wet Tropical Forest At
Joumalof Biogeography (I1996) 23, 467-475 Phenologyof Ficusvariegata in a seasonalwet tropicalforest at Cape Tribulation,Australia HUGH SPENCER', GEORGE WEIBLENI 2* AND BRIGITTA FLICK' 'Cape TribulationResearch Station, Private Mail Bag5, Cape Tribulationvia Mossman,Queensland 4873, Australiaand 2 The Harvard UniversityHerbaria, 22 Divinity Avenue,Cambridge, Massachusetts 02138, USA Abstract. We studiedthe phenologyof 198 maturetrees dioecious species, female and male trees initiatedtheir of the dioecious figFicus variegataBlume (Moraceae) in a maximalfig crops at differenttimes and floweringwas to seasonally wet tropical rain forestat Cape Tribulation, some extentsynchronized within sexes. Fig productionin Australia, from March 1988 to February 1993. Leaf the female (seed-producing)trees was typicallyconfined productionwas highlyseasonal and correlatedwith rainfall. to the wet season. Male (wasp-producing)trees were less Treeswere annually deciduous, with a pronouncedleaf drop synchronizedthan femaletrees but reacheda peak level of and a pulse of new growthduring the August-September figproduction in the monthsprior to the onset of female drought. At the population level, figs were produced figproduction. Male treeswere also morelikely to produce continuallythroughout the study but there were pronounced figscontinually. Asynchrony among male figcrops during annual cyclesin figabundance. Figs were least abundant the dry season could maintainthe pollinatorpopulation duringthe early dry period (June-September)and most under adverseconditions -
Corner, Mainly Melanesian
New species of Streblus and Ficus (Moraceae) E.J.H. Corner Botany School, University of Cambridge, U.K. Summary New — Lour. S. Taxa. Streblus sect. Protostreblus, sect. nov., with the single species ascendens sp. nov. (Solomon Isl.); S. sclerophyllus sp. nou. (sect. Paratrophis, New Caledonia). Ficus F. cristobalensis var. malaitana var. nov. (subgen. Pharmacosycea, Solomon Isl.); hesperia sp. nov. (sect. Solomon servula and Sycidium, Isl.); F. sp. nov. F. lapidaria sp. nov. (sect. Adenosperma, New Guinea); F. novahibernica and F. cryptosyce (sect. Sycocarpus, New Ireland, New Guinea). Notes are given on Streblus pendulinus, S. solomonensis, Ficus illiberalis, F. subtrinervia (Solomon Isl.), F. adenosperma (Rotuma), and F. subcuneata with a key to its allies. Streblus Lour. sect. Protostreblus sect. nov. Folia spiraliter disposita; lamina ovata v. subcordata, costis basalibus ad mediam laminam elongatis, intercostis transversalibus numerosis. Inflorescentia ut in sect. Paratro- phis; embryo radicula incumbenti elongata, cotyledonibus foliaceis subincrassatis con- duplicatis. Cystolitha nulla. — Typus: S. ascendens, Insulis Solomonensibus. The structural peculiarity of this new section lies in the combinationof the Moras-like leafwith the reproductive characters of Streblus sect. Paratrophis. The ovate subcordate lamina with prominent basal veins and numerous transverse intercostals is unknown in Streblus. the rest of The lax spiral arrangement of the leaves is clearly antecedent to the distichous which also the of the prevails in rest genus. In various Moraceae, such as Ficus, Artocarpus, Maclura, and Broussonetia in the broad sense in which I understand them (Corner, 1962), the transition from the spiral arrangement to the distichous is manifest as the twig becomes more horizontal in its growth and develops applanate, in contrast with Thus this section be of the ascending, foliage. -
Ficus Plants for Hawai'i Landscapes
Ornamentals and Flowers May 2007 OF-34 Ficus Plants for Hawai‘i Landscapes Melvin Wong Department of Tropical Plant and Soil Sciences icus, the fig genus, is part of the family Moraceae. Many ornamental Ficus species exist, and probably FJackfruit, breadfruit, cecropia, and mulberry also the most colorful one is Ficus elastica ‘Schrijveriana’ belong to this family. The objective of this publication (Fig. 8). Other Ficus elastica cultivars are ‘Abidjan’ (Fig. is to list the common fig plants used in landscaping and 9), ‘Decora’ (Fig. 10), ‘Asahi’ (Fig. 11), and ‘Gold’ (Fig. identify some of the species found in botanical gardens 12). Other banyan trees are Ficus lacor (pakur tree), in Hawai‘i. which can be seen at Foster Garden, O‘ahu, Ficus When we think of ficus (banyan) trees, we often think benjamina ‘Comosa’ (comosa benjamina, Fig. 13), of large trees with aerial roots. This is certainly accurate which can be seen on the UH Mänoa campus, Ficus for Ficus benghalensis (Indian banyan), Ficus micro neriifolia ‘Nemoralis’ (Fig. 14), which can be seen at carpa (Chinese banyan), and many others. Ficus the UH Lyon Arboretum, and Ficus rubiginosa (rusty benghalensis (Indian banyan, Fig. 1) are the large ban fig, Fig. 15). yans located in the center of Thomas Square in Hono In tropical rain forests, many birds and other animals lulu; the species is also featured in Disneyland (although feed on the fruits of different Ficus species. In Hawaii the tree there is artificial). Ficus microcarpa (Chinese this can be a negative feature, because large numbers of banyan, Fig. -
The Castilleae, a Tribe of the Moraceae, Renamed and Redefined Due to the Exclusion of the Type Genus Olmedia From
Bot. Neerl. Ada 26(1), February 1977, p. 73-82, The Castilleae, a tribe of the Moraceae, renamed and redefined due to the exclusion of the type genus Olmedia from the “Olmedieae” C.C. Berg Instituut voor Systematische Plantkunde, Utrecht SUMMARY New data on in the of Moraceae which known cladoptosis group was up to now as the tribe Olmedieae led to a reconsideration ofthe position ofOlmedia, and Antiaropsis , Sparattosyce. The remainder ofthe tribe is redefined and is named Castilleae. 1. INTRODUCTION The monotypic genus Olmedia occupies an isolated position within the neo- tropical Olmedieae. Its staminate flowers have valvate tepals, inflexed stamens springing back elastically at anthesis, and sometimes well-developed pistil- lodes. Current anatomical research on the wood of Moraceae (by Dr. A. M. W. Mennega) and recent field studies (by the present author) revealed that Olmedia is also distinct in anatomical characters of the wood and because of the lack of self-pruning branches. These differences between Olmedia and the other representatives of the tribe demand for reconsideration of the position of the genus and the deliminationof the tribe. The Olmedia described The genus was by Ruiz & Pavon (1794). original description mentioned that the stamens bend outward elastically at anthesis. Nevertheless it was placed in the “Artocarpeae” (cf. Endlicher 1836-1840; Trecul 1847), whereas it should have been placed in the “Moreae” on ac- of of count the characters the stamens which were rather exclusively used for separating the two taxa. Remarkably Trecul (1847) in his careful study on the “Artocarpeae” disregarded the (described) features of the stamens. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
Vascular Plant Families of the United States Grouped by Diagnostic Features
Humboldt State University Digital Commons @ Humboldt State University Botanical Studies Open Educational Resources and Data 12-6-2019 Vascular Plant Families of the United States Grouped by Diagnostic Features James P. Smith Jr Humboldt State University, [email protected] Follow this and additional works at: https://digitalcommons.humboldt.edu/botany_jps Part of the Botany Commons Recommended Citation Smith, James P. Jr, "Vascular Plant Families of the United States Grouped by Diagnostic Features" (2019). Botanical Studies. 96. https://digitalcommons.humboldt.edu/botany_jps/96 This Flora of the United States and North America is brought to you for free and open access by the Open Educational Resources and Data at Digital Commons @ Humboldt State University. It has been accepted for inclusion in Botanical Studies by an authorized administrator of Digital Commons @ Humboldt State University. For more information, please contact [email protected]. FLOWERING PLANT FAMILIES OF THE UNITED STATES GROUPED BY DIAGNOSTIC FEATURES James P. Smith, Jr. Professor Emeritus of Botany Department of Biological Sciences Humboldt State University Second edition — 6 December 2019 The focus is on families of plants found in the conterminous United States, including ornamentals. The listing of a family is not meant to imply that every species has that feature. I am using a fewfamily names, such as Liliaceae, Plantaginaceae, and Scrophulariaceae, in the traditional sense, because their limits remain unsettled. Parasitic on branches Dioscoreaceae -
Biogeography, Phylogeny and Divergence Date Estimates of Artocarpus (Moraceae)
Annals of Botany 119: 611–627, 2017 doi:10.1093/aob/mcw249, available online at www.aob.oxfordjournals.org Out of Borneo: biogeography, phylogeny and divergence date estimates of Artocarpus (Moraceae) Evelyn W. Williams1,*, Elliot M. Gardner1,2, Robert Harris III2,†, Arunrat Chaveerach3, Joan T. Pereira4 and Nyree J. C. Zerega1,2,* 1Chicago Botanic Garden, Plant Science and Conservation, 1000 Lake Cook Road, Glencoe, IL 60022, USA, 2Northwestern University, Plant Biology and Conservation Program, 2205 Tech Dr., Evanston, IL 60208, USA, 3Faculty of Science, Genetics Downloaded from https://academic.oup.com/aob/article/119/4/611/2884288 by guest on 03 January 2021 and Environmental Toxicology Research Group, Khon Kaen University, 123 Mittraphap Highway, Khon Kaen, 40002, Thailand and 4Forest Research Centre, Sabah Forestry Department, PO Box 407, 90715 Sandakan, Sabah, Malaysia *For correspondence. E-mail [email protected], [email protected] †Present address: Carleton College, Biology Department, One North College St., Northfield, MN 55057, USA. Received: 25 March 2016 Returned for revision: 1 August 2016 Editorial decision: 3 November 2016 Published electronically: 10 January 2017 Background and Aims The breadfruit genus (Artocarpus, Moraceae) includes valuable underutilized fruit tree crops with a centre of diversity in Southeast Asia. It belongs to the monophyletic tribe Artocarpeae, whose only other members include two small neotropical genera. This study aimed to reconstruct the phylogeny, estimate diver- gence dates and infer ancestral ranges of Artocarpeae, especially Artocarpus, to better understand spatial and tem- poral evolutionary relationships and dispersal patterns in a geologically complex region. Methods To investigate the phylogeny and biogeography of Artocarpeae, this study used Bayesian and maximum likelihood approaches to analyze DNA sequences from six plastid and two nuclear regions from 75% of Artocarpus species, both neotropical Artocarpeae genera, and members of all other Moraceae tribes. -
WESTERN AUSTRALIA's JOURNAL of SYSTEMATIC BOTANY G Dixon
WESTERN AUSTRALIA’S JOURNAL OF SYSTEMATIC BOTANY ISSN 0085-4417 G Dixon D.J. Ficus carpentariensis – a new sandpaper fig for northern Australia and a revision of the F. opposita complex (Moraceae: Ficus subg. Ficus sect. Sycidium informal group F. copiosa) Nuytsia 16(2): 269–284 (2007) All enquiries and manuscripts should be directed to: The Editor – NUYTSIA Western Australian Herbarium Telephone: +61 8 9334 0500 Dept of Environment and Conservation Facsimile: +61 8 9334 0515 Locked Bag 104 Bentley Delivery Centre Email: [email protected] Western Australia 6983 Web: science.dec.wa.gov.au/nuytsia/ AUSTRALIA All material in this journal is copyright and may not be reproduced except with the written permission of the publishers. © Copyright Department of Environment and Conservation . D.J.Nuytsia Dixon, 16(2):269–284 Ficus carpentariensis (2007) – a new sandpaper fi g for northern Australia 269 Ficus carpentariensis – a new sandpaper fi g for northern Australia and a revision of the F. opposita complex (Moraceae: Ficus subg. Ficus sect. Sycidium informal group F. copiosa) Dale J. Dixon Northern Territory Herbarium, Department of Natural Resources, Environment and the Arts, P.O. Box 496 Palmerston, Northern Territory, 0831 Australia Abstract Dixon D.J. Ficus carpentariensis – a new sandpaper fi g for northern Australia and a revision of the F. opposita complex (Moraceae: Ficus subg. Ficus sect. Sycidium informal group F. copiosa). Nuytsia 16(2): 269–284 (2007). The Ficus opposita Miq. complex is revised. Four taxa in three species are recognized, F. opposita from Queensland and Papua New Guinea, Ficus aculeata Miq. with two varieties, one, var. -
First Steps Towards a Floral Structural Characterization of the Major Rosid Subclades
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2006 First steps towards a floral structural characterization of the major rosid subclades Endress, P K ; Matthews, M L Abstract: A survey of our own comparative studies on several larger clades of rosids and over 1400 original publications on rosid flowers shows that floral structural features support to various degrees the supraordinal relationships in rosids proposed by molecular phylogenetic studies. However, as many apparent relationships are not yet well resolved, the structural support also remains tentative. Some of the features that turned out to be of interest in the present study had not previously been considered in earlier supraordinal studies. The strongest floral structural support is for malvids (Brassicales, Malvales, Sapindales), which reflects the strong support of phylogenetic analyses. Somewhat less structurally supported are the COM (Celastrales, Oxalidales, Malpighiales) and the nitrogen-fixing (Cucurbitales, Fagales, Fabales, Rosales) clades of fabids, which are both also only weakly supported in phylogenetic analyses. The sister pairs, Cucurbitales plus Fagales, and Malvales plus Sapindales, are structurally only weakly supported, and for the entire fabids there is no clear support by the present floral structural data. However, an additional grouping, the COM clade plus malvids, shares some interesting features but does not appear as a clade in phylogenetic analyses. Thus it appears that the deepest split within eurosids- that between fabids and malvids - in molecular phylogenetic analyses (however weakly supported) is not matched by the present structural data. Features of ovules including thickness of integuments, thickness of nucellus, and degree of ovular curvature, appear to be especially interesting for higher level relationships and should be further explored. -
Maclura Pomifera Osage Orange Moraceae
Maclura pomifera Osage orange Moraceae Forest Starr, Kim Starr, and Lloyd Loope United States Geological Survey--Biological Resources Division Haleakala Field Station, Maui, Hawai'i October, 2003 OVERVIEW Maclura pomifera (osage orange) is a thorny, dioecious tree, native to a narrow band near Texas and Arkansas, and widely planted throughout North America and southern Canada for windbreaks and fence posts. Maclura pomifera has become naturalized in areas where it has been planted. Maclura pomifera is considered a pest plant in Italy and is being monitored for invasive potential in Spain where it is cultivated (Dana et al. 2001). Recently, a single hedge of Maclura pomifera was discovered in Ha'iku, Maui. In addition, Skolmen (1960) reports that Maclura pomifera was used as a forestry tree and was planted on Moloka'i, Hawai'i, and Maui. The status of these forestry plantings is not known and needs further investigation. The hedge in Ha'iku appears to show no sign of regeneration yet and only un-ripened female fruits have been observed. With an invasive history and limited distribution on Maui, this species is a good candidate for eradication before it becomes naturalized. It should also be prevented from further use in plantings through education and, or by adding it to the state noxious weed list. TAXONOMY Family: Moraceae (Mulberry family) (Wagner et al. 1999). Latin name: Maclura pomifera (Raf.) Schneid. (PLANTS 2003). Synonyms: Ioxylon pomiferum Raf., Toxylon pomiferum Raf. ex Sarg (PLANTS 2003). Common names: Osage orange (PLANTS 2003), hedge apple, bois d'arc (Carey 1994). Taxonomic notes: The genus, Maclura, is comprised of a single dioecious species, Maclura pomifera. -
Hairy Crabweed
Hairy Crabweed Figure 1. Hairy crabweed seedlings. Figure 2. Mature hairy crabweed. Figure 3. Flower clusters in leaf axils. Hairy crabweed (Fatoua villosa), also known as be thrown up to 4 feet as a form of natural dispersal. Seeds mulberryweed, is an introduced annual in the mulberry germinate in warm weather (60–100°F), maturing within 12 family. Hairy crabweed is native to East Asia and was days after reaching the two-leaf stage. This maturity rate likely introduced to Louisiana around 1964. Other reports makes eradication difficult without persistent monitoring indicate that it escaped around New Orleans in the 1950s, of the site. perhaps by contaminated equipment brought back to the United States after World War II. Compared with Habitat other invasive plants, hairy crabweed is a fairly recent Hairy crabweed plants prefer moist areas in sun or introduction, yet it occurs over much of the United States shade, but mostly in shade. Landowners purchasing today. Hairy crabweed seems to avoid detection often until nursery plants should be cautious. Even though hairy it is well established on a site. This is possibly because crabweed may not be visible in the container, seeds may be of its similar appearance to seedling mulberry trees. In in the soil. Seeds can be thrown into containers by nearby addition, plants can produce seedlings around 1 inch tall, plants and go unnoticed until they germinate. Once in a making it difficult to detect while it becomes established. suitable habitat in the landscape, it will proliferate without eradication. Hairy crabweed adapts to a wide range of Description habitats, including sun to shade and wet to moderately With the common name of mulberryweed, hairy moist soils.