Mixed Farm As Habitat for Grizzled Leaf Monkey (Presbytis Comata) Population
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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. -
The Systematic Wood Anatomy of the Moraceae (Urticales) V. Genera of the Tribe Moreae Without Urticaceous Stamens *
IAWA Bulletin n.s., Vol. 7 (3),1986 175 THE SYSTEMATIC WOOD ANATOMY OF THE MORACEAE (URTICALES) V. GENERA OF THE TRIBE MOREAE WITHOUT URTICACEOUS STAMENS * by B.1. H. ter Welle, 1. Koek-Noorman and S. M. C. Topper Institute of Systematic Botany, University of Utrecht, Heidelberglaan 2, 3508 TC Utrecht, The Netherlands Summary The wood anatomy of the Moreae without based upon these characters, however (Berg, urticaceous stamens is described in detail. Ge 1983), is not in accordance with the tribes neric descriptions of the following genera are Moreae and Artocarpeae sensu Corner (1962). provided: Antiaropsis, Artocarpus, Bagassa, Ba Both Berg's and Corner's subdivisions deviate tocarpus, Clarisia, Parartocarpus, Poulsenia, from older classifications, as given by, for in Prainea, Sorocea, Sparattosyce, and Treculia. stance, Bentham and Hooker (1880) and Engler Wood anatomical variation below the genus (1888). level is very limited, except in the genus Clari The Moreae characterised by the absence of sia. Intergeneric variation, however, is much urticaceous stamens comprise the genera Antia more evident. Most genera can be recognised ropsis (New Guinea), Artocarpus (Southeast by the presence or absence of septate fibres, Asia), Bagassa (Neotropics), Batocarpus (Neo and of radial latex tubes, the size of the inter tropics), Clarisia (Neotropics), Hullettia (South vascular pits, the parenchyma distribution, and east Asia),Parartocarpus (Southeast Asia), Poul crystal distribution. The diagnostic and taxon senia (Neotropics), Prainea (Malesia), Sorocea omic value of several characters is discussed. (Neotropics), Sparattosyce (New Caledonia), Key words: Moraceae, Moreae, systematic wood and Treculia (Tropical Africa). anatomy. Methods and Materials In troduction The methods employed are those given in This paper is part of a series, in which the the first paper of this series (Koek-Noorman et wood anatomy of the Moraceae is described aI., 1984). -
Flora Malesiana Precursor for the Treatment of Moraceae 8: Other Genera Than Ficus
BLUMEA 50: 535 –550 Published on 14 December 2005 http://dx.doi.org/10.3767/000651905X622815 FLORA MALESIANA PRECURSOR FOR THE TREATMENT OF MORACEAE 8: OTHER GENERA THAN FICUS C.C. BERG Bergen Museum, University of Bergen, Allégate 41, 5007 Bergen, Norway; Nationaal Herbarium Nederland, Universiteit Leiden branch, P.O. Box 9514, 2300 RA Leiden, The Netherlands. SUMMARY The tribe Artocarpeae is redefined, the tribe Soroceae is established by change of rank, and as a consequence a new tribe Antiaropsidae is established. Moreover, a new species Antiaropsis uniflora C.C. Berg is described. In Artocarpus a new species is described, A. albobrunneus C.C. Berg, one subspecies is raised to the rank of species, A. brevipedunculatus (F.M. Jarrett) C.C. Berg, and new subspecies are described in several species, A. longifolius Becc. subsp. adpressus C.C. Berg, A. teijs- mannii Miq. subsp. subglabrus C.C. Berg. In Prainea, P. papuana is reduced to a subspecies, P. limpato (Miq.) K. Heyne subsp. papuana (Becc.) C.C. Berg. In Streblus the sections Pseudomorus (Bureau) Corner and Taxotrophis (Blume) Corner are reinstated, S. urophyllus is reduced to a subspecies, S. glaber (Merr.) Corner subsp. urophyllus (Diels) C.C. Berg, in S. streblus var. australianus is raised to S. glaber subsp. australianus (C.T. White) C.C. Berg, and S. celebensis C.C. Berg is described as a new species. Key words: Moraceae, Artocarpeae, Antiaropsis, Artocarpus, Prainea, Streblus, Malesia. INTRODUCTION A precursory study on Moraceae focussed on its classification and the Asian repre- sentatives was published by Corner in 1962. It was preceded by a monographic study on Artocarpus and allied genera by Jarrett (1959a, b, c, 1960a, b). -
Perennial Edible Fruits of the Tropics: an and Taxonomists Throughout the World Who Have Left Inventory
United States Department of Agriculture Perennial Edible Fruits Agricultural Research Service of the Tropics Agriculture Handbook No. 642 An Inventory t Abstract Acknowledgments Martin, Franklin W., Carl W. Cannpbell, Ruth M. Puberté. We owe first thanks to the botanists, horticulturists 1987 Perennial Edible Fruits of the Tropics: An and taxonomists throughout the world who have left Inventory. U.S. Department of Agriculture, written records of the fruits they encountered. Agriculture Handbook No. 642, 252 p., illus. Second, we thank Richard A. Hamilton, who read and The edible fruits of the Tropics are nnany in number, criticized the major part of the manuscript. His help varied in form, and irregular in distribution. They can be was invaluable. categorized as major or minor. Only about 300 Tropical fruits can be considered great. These are outstanding We also thank the many individuals who read, criti- in one or more of the following: Size, beauty, flavor, and cized, or contributed to various parts of the book. In nutritional value. In contrast are the more than 3,000 alphabetical order, they are Susan Abraham (Indian fruits that can be considered minor, limited severely by fruits), Herbert Barrett (citrus fruits), Jose Calzada one or more defects, such as very small size, poor taste Benza (fruits of Peru), Clarkson (South African fruits), or appeal, limited adaptability, or limited distribution. William 0. Cooper (citrus fruits), Derek Cormack The major fruits are not all well known. Some excellent (arrangements for review in Africa), Milton de Albu- fruits which rival the commercialized greatest are still querque (Brazilian fruits), Enriquito D. -
(Moraceae) with a Focus on Artocarpus
Systematic Botany (2010), 35(4): pp. 766–782 © Copyright 2010 by the American Society of Plant Taxonomists DOI 10.1600/036364410X539853 Phylogeny and Recircumscription of Artocarpeae (Moraceae) with a Focus on Artocarpus Nyree J. C. Zerega, 1 , 2 , 5 M. N. Nur Supardi , 3 and Timothy J. Motley 4 1 Chicago Botanic Garden, 1000 Lake Cook Road, Glencoe, Illinois 60022, U. S. A. 2 Northwestern University, Plant Biology and Conservation, 2205 Tech Drive, Evanston, Illinois 60208, U. S. A. 3 Forest Research Institute of Malaysia, 52109, Kepong, Selangor Darul Ehsan, Malaysia 4 Old Dominion University, Department of Biological Sciences, 110 Mills Godwin Building/45th Street, Norfolk, Virginia 23529-0266, U. S. A. 5 Corresponding author ( [email protected] ) Communicating Editor: Anne Bruneau Abstract— Moraceae is a large (~1,050 species) primarily tropical family with several economically and ecologically important species. While its monophyly has been well supported in recent studies, relationships within the family at the tribal level and below remain unresolved. Delimitation of the tribe Artocarpeae has been particularly difficult. Classifications based on morphology differ from those based on phyloge- netic studies, and all treatments include highly heterogeneous assemblages of genera that seem to represent a cross section of the family. We evaluated chloroplast and nuclear DNA sequence data for 60 Moraceae taxa representing all genera that have been included in past treatments of Artocarpeae and also included species from several other Moraceae tribes and closely related families as outgroups. The data were analyzed using maximum parsimony and maximum likelihood methods and indicate that none of the past treatments of Artocarpeae represent a mono- phyletic lineage. -
The Systematic Wood Anatomy of the Moraceae (Uriticales)
lAWA Bulletin Vol. 7 1986 n.s., (3), 175 The systematic wood anatomy of the Moraceae (Uriticales). V. Genera of the tribe Moreae without urticaceous stamens* by B.J.H. ter Welle J. Koek-Noorman and S.M.C. Topper Institute ofSystematic Botany, University of Utrecht, Heidelberglaan2, 3508 TC Utrecht, The Netherlands Summary The wood anatomy of the Moreae without based upon these characters, however (Berg, urticaceous stamens is described in detail. Ge- 1983), is not in accordance with the tribes neric descriptions of the following genera are Moreae and Artocarpeae sensu Corner (1962). provided: Antiaropsis, Artocarpus, Bagassa, Ba- Both Berg’s and Corner’s subdivisions deviate tocarpus, Clarisia, Parartocarpus, Poulsenia, from older classifications, as given by, for in- Prainea, Sorocea, Sparattosyce, and Treculia. stance, Bentham and Hooker (1880) and Engler Wood anatomical variation below the genus (1888). level is very limited, except in the genus Clari- The Moreae characterised by the absence of sia. Intergeneric variation, however, is much urticaceous stamens comprise the genera Antia- more evident. Most genera can be recognised ropsis (New Guinea), Artocarpus (Southeast by the presence or absence of septate fibres, Asia), Bagassa (Neotropics), Batocarpus (Neo- and of radial latex tubes, the size of the inter- tropics), Clarisia (Ncotropics), Huliettia (South- vascular pits, the parenchyma distribution,and east Asia),Parartocarpus (Southeast Asia), Poul- crystal distribution. The diagnostic and taxon- senia (Neotropics), Prainea (Malesia), Sorocea omic value of several characters is discussed. (Neotropics), Sparattosyce (New Caledonia), Key words: Moraceae, Moreae, systematic wood and Treculia (Tropical Africa). anatomy Methods and Materials Introduction The methods employed are those given in This is of in which the the first of this paper part a series, paper series (Koek-Noorman et wood anatomy of the Moraceae is described al., 1984). -
MORACEAE Genera Other Than FICUS (C.C
Flora Malesiana, Series I, Volume 17 / Part 1 (2006) 1–152 MORACEAE GENera OTHer THAN FICUS (C.C. Berg, E.J.H. Corner† & F.M. Jarrett)1 FOREWORD The following treatments of Artocarpus, Hullettia, Parartocarpus, and Prainea are based on the monograph by Jarrett (1959–1960) and on the treatments she made for this Flora in cooperation with Dr. M. Jacobs in the 1970s. These included some new Artocarpus species described in 1975 and the re-instatement of A. peltata. Artocarpus lanceifolius subsp. clementis was reduced to the species, in A. nitidus the subspe- cies borneensis and griffithii were reduced to varieties and the subspecies humilis and lingnanensis included in var. nitidus. The varieties of A. vrieseanus were no longer recognised. More new Malesian species of Parartocarpus were described by Corner (1976), Go (1998), and in Artocarpus by Kochummen (1998). A manuscript with the treatment of the other genera was submitted by Corner in 1972. Numerous changes to the taxonomy, descriptions, and keys have been made to the original manuscripts, for which the present first author is fully responsible. References: Corner, E.J.H., A new species of Parartocarpus Baillon (Moraceae). Gard. Bull. Singa- pore 28 (1976) 183–190. — Go, R., A new species of Parartocarpus (Moraceae) from Sabah. Sandaka- nia 12 (1998) 1–5. — Jarrett, F.M., Studies in Artocarpus and allied genera I–V. J. Arnold Arbor. 50 (1959) 1–37, 113–155, 298–368; 51 (1960) 73–140, 320–340. — Jarrett, F.M., Four new Artocarpus species from Indo-Malesia (Moraceae). Blumea 22 (1975) 409–410. — Kochummen, K.M., New species and varieties of Moraceae from Malaysia. -
50159-001: Protecting and Investing in Natural Capital in Asia and The
Technical Assistance Consultant’s Report Project Number: 50159-001 October 2019 Technical Assistance Number: 9461 Regional: Protecting and Investing in Natural Capital in Asia and the Pacific (Cofinanced by the Climate Change Fund and the Global Environment Facility) Prepared by: Lorenzo V. Cordova, Jr. MA and Prof. Pastor L. Malabrigo, Jr. PRO-SEEDS DEVELOPMENT ASSOCIATION, INC. Los Banos, Laguna, Philippines Asian Development Bank is the executing and implementing agency. This consultant’s report does not necessarily reflect the views of ADB or the Government concerned, and ADB and the Government cannot be held liable for its contents. (For project preparatory technical assistance: All the views expressed herein may not be incorporated into the proposed project’s design. Nature-Based Solutions for New Clark City ASSESSMENT OF DESIGN STANDARD AND GUIDELINES, AND SCOPING RESULTS OF PROPOSED SUSTAINABILITY MANAGEMENT UNIT Lorenzo V. Cordova, Jr. EnP Prof. Pastor L. Malabrigo, Jr. October 2019 A report submitted to: Asian Development Bank 1 Table of Contents I. Background and Introduction ............................................................................................................. 4 II. Overview of Activities and Framework ............................................................................................. 5 III. Assessment of Chapter 8 of New Clark City Phase 1 Design Standards and Guidelines ..... 7 3.1. Landscape beauty in harmony with nature ................................................................................... -
Molecular Recircumscription of Broussonetia (Moraceae) and the Identity and Taxonomic Status of B. Kaempferi Var. Australis
Chung et al. Bot Stud (2017) 58:11 DOI 10.1186/s40529-017-0165-y ORIGINAL ARTICLE Open Access Molecular recircumscription of Broussonetia (Moraceae) and the identity and taxonomic status of B. kaempferi var. australis Kuo‑Fang Chung1,2*, Wen‑Hsi Kuo1, Yi‑Hsuan Hsu1,2, Yi‑Hsuan Li1,2, Rosario Rivera Rubite3 and Wei‑Bin Xu4 Abstract Background: Despite being a relatively small genus, the taxonomy of the paper mulberry genus Broussonetia remains problematic. Much of the controversy is related to the identity and taxonomic status of Broussonetia kaemp- feri var. australis, a name treated as a synonym in the floras of Taiwan and yet accepted in the floras of China. At the generic level, the monophyly of Corner (Gard Bull Singap 19:187–252, 1962)’s concept of Broussonetia has not been tested. In recent studies of Broussonetia of Japan, lectotypes of the genus were designated and three species (B. kaempferi, Broussonetia monoica, and Broussonetia papyrifera) and a hybrid (B. kazinoki) were recognized. Based on the revision and molecular phylogenetic analyses, this article aims to clarify these× issues. Results: Herbarium studies, field work, and molecular phylogenetic analyses indicate that all Taiwanese materials identifiable to B. kaempferi var. australis are conspecific with B. monoica of Japan and China. Molecular phylogenetic analyses showed that Broussonetia sensu Corner (Gard Bull Singap 19:187–252, 1962) contains two clades correspond‑ ing to sect. Broussonetia and sect. Allaeanthus, with Malaisia scandens sister to sect. Broussonetia. Conclusions: Based on our analyses, B. kaempferi var. australis is treated as a synonym of B. monoica and that B. -
Ficus Spp. (And Other Important Moraceae) 1699 Breaches of the NVC Increasing Steadily to More Than House SM (1997) Reproductive Biology of Eucalypts
TROPICAL ECOSYSTEMS / Ficus spp. (and other important Moraceae) 1699 breaches of the NVC increasing steadily to more than House SM (1997) Reproductive biology of eucalypts. In: 200 per year, with only seven prosecutions com- Williams JE and Woinarski JCZ (eds) Eucalypt Ecology: menced out of more than 700 alleged breaches from Individuals to Ecosystems, pp. 30–55. Cambridge, UK: 1998 to April 2002. Cambridge University Press. There are many implications of the changes to the Keith H (1997) Nutrient cycling in eucalypt ecosystems. In: eucalypt forests across Australia. The clearing of Williams JE and Woinarski JCZ (eds) Eucalypt Ecology: Individuals to Ecosystems, pp. 197–226. Cambridge, native habitat is the single most threatening process UK: Cambridge University Press. for biodiversity loss and species extinction in Kirkpatrick JB (1997) Vascular plant–eucalypt interac- Australia. The loss of species in Australia over the tions. In: Williams JE and Woinarski JCZ (eds) Eucalypt past two centuries due to human impact is con- Ecology: Individuals to Ecosystems, pp. 227–245. Cam- servatively estimated at 97 plants, 17 species of bridge, UK: Cambridge University Press. mammal, and three birds. However, several hundred Landsberg JJ and Cork SJ (1997) Herbivory: Interactions vertebrates, several thousand plants, and an untold between eucalypts and the vertebrates and invertebrates number of invertebrates are threatened with extinc- that feed on them. In: Williams JE and Woinarski JCZ tion due to loss of habitat. The extent and rate (eds) Eucalypt Ecology: Individuals to Ecosystems, pp. of deforestation in Queensland are comparable to 342–372. Cambridge, UK: Cambridge University Press. that in Western Australia and Victoria in the May TW and Simpson JA (1997) Fungal diversity and ecology in eucalypt ecosystems. -
An Update on Antitumor Activity of Naturally Occurring Chalcones
Hindawi Publishing Corporation Evidence-Based Complementary and Alternative Medicine Volume 2013, Article ID 815621, 22 pages http://dx.doi.org/10.1155/2013/815621 Review Article An Update on Antitumor Activity of Naturally Occurring Chalcones En-Hui Zhang,1 Ru-Feng Wang,1 Shu-Zhen Guo,2 and Bin Liu1 1 School of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100102, China 2 School of Preclinical Medicine, Beijing University of Chinese Medicine, Beijing 100029, China Correspondence should be addressed to Bin Liu; [email protected] Received 15 January 2013; Accepted 19 March 2013 Academic Editor: Yoshiyuki Kimura Copyright © 2013 En-Hui Zhang 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. Chalcones, which have characteristic 1,3-diaryl-2-propen-1-one skeleton, are mainly produced in roots, rhizomes, heartwood, leaves, and seeds of genera Angelica,Sophora,Glycyrrhiza,Humulus,Scutellaria,Parartocarpus,Ficus,Dorstenia,Morus,Artocarpus, and so forth. They have become of interest in the research and development of natural antitumor agents over the past decades due to their broad range of mechanisms including anti-initiation, induction of apoptosis, antiproliferation, antimetastasis, antiangiogenesis, and so forth. This review summarizes the studies on the antitumor activity of naturally occurring chalcones and their underlying mechanisms in detail during the past decades. 1. Introduction biosynthesis of flavonoids. Structurally, they are a group of compounds bearing 1,3-diaryl-2-propen-1-one framework, Chalcones are one of the subclasses of flavonoid family. -
Of Papua New Guinea Are Very Good Quality Foods
1 Food Crops of Papua New Guinea An introduction to the crops, their importance and distribution in Papua New Guinea Bruce R French 2 Dedication This book is dedicated to our Creator who has made about 20,000 edible plant species. The Psalmist and other writers in the Bible say that God actually enjoys his Creation. He also asked us to be good stewards of His world. This book is therefore dedicated to the many subsistence farmers who do this well, taking care of His world and especially to those who enjoy doing it. The author Bruce French has enjoyed visiting and working in Papua New Guinea during many trips from 1967 until the present. He now lives in Tasmania and continues to search for information on the edible plants of the world and how they could be better used to help hungry people feed themselves. Present address: 38 West St., Burnie, Tasmania 7320 Australia Phone (03) 64321080 Email: [email protected] If you are wanting more detailed or specific information on plants there is a database on CD covering all the edible plants known to be in Papua New Guinea. Publication date 2006 1 Contents 1. Introduction 2 2. Root crops and staple foods 3 3. Kumus or Green leafy vegetables 13 4. Vegetables 23 5. Beans 29 6. Tree fruits 39 7. Nuts 51 8. Shrub and vine fruit 59 2 Introduction Papua New Guinea is often spoken of as the land of diversity with many different cultures, languages, plants and animals. This is also true of the food plants that people grow and eat.