A Guide to Curating New World Melastomataceae Collections with a Linear Generic Sequence to World-Wide Melastomataceae
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Appreciably Modified
VI1.-KEYS TO THE GESER.1 AND SUBGEKERA OF ASTS BY WM. 31. WHEELER KEYTO THE SUBFAMILIES~ 8, 0 1. Cloacal orifice round, tefminal, surrounded by a fringe of hairs; sting transformed into a sustentacular apparatus for the orifice of the poison vesicle, which has a peculiar structure called by Fore1 '' pulviniferous vesicle" (vessie 2 coussinet) . Abdominal pedicel consisting of a single segment; no constriction between the second and third segments. Male genitalia not retractile. Nymphs rarely naked, most frequently enclosed in a cocoon. FORMICINA3. Cloacal orifice in the shape of a slit. ........................ .2. 2. Sting rudimentary (except Aneuretus) ; abdominal pedicel con- sisting of a single segment; no constriction between the second and third segments of the abdomen; the poison glands are often vestigial and there are anal glands which secrete an aromatic product of characteristic odor (Tapinoma-odor). Nymphs without a cocoon. ..........DOLICHODERINAE. Sting developed, though sometimes very small, but capable never- theless of being exserted from the abdomen. The first two segments of the abdomen usually modified, either forming together a two-jointed pedicel, or the first alone (petiole) forming the pedicel, the second (postpetiole) being merely constricted posteriorly and articulating with a spheroidal surface of the third segment, which is usually transversely striated (stridulatory organ) ; rarely the second segment is not appreciably modified. .................................... .3. 3. Pedicel of two segments, the petiole and the postpetiole; rarely (in Melissotarsus, e. 9.) the postpetiole is attached to the follow- ing segment over its whole extent. Frontal carin= usually separated from each other (except in the Melissotarsini and certain Attini). In the male the copulatory organs are almost always exserted (being entirely retractile in certain genera of the Solenopsidini only) ; cerci nearly always present (except Anergates) . -
New Zealand's Genetic Diversity
1.13 NEW ZEALAND’S GENETIC DIVERSITY NEW ZEALAND’S GENETIC DIVERSITY Dennis P. Gordon National Institute of Water and Atmospheric Research, Private Bag 14901, Kilbirnie, Wellington 6022, New Zealand ABSTRACT: The known genetic diversity represented by the New Zealand biota is reviewed and summarised, largely based on a recently published New Zealand inventory of biodiversity. All kingdoms and eukaryote phyla are covered, updated to refl ect the latest phylogenetic view of Eukaryota. The total known biota comprises a nominal 57 406 species (c. 48 640 described). Subtraction of the 4889 naturalised-alien species gives a biota of 52 517 native species. A minimum (the status of a number of the unnamed species is uncertain) of 27 380 (52%) of these species are endemic (cf. 26% for Fungi, 38% for all marine species, 46% for marine Animalia, 68% for all Animalia, 78% for vascular plants and 91% for terrestrial Animalia). In passing, examples are given both of the roles of the major taxa in providing ecosystem services and of the use of genetic resources in the New Zealand economy. Key words: Animalia, Chromista, freshwater, Fungi, genetic diversity, marine, New Zealand, Prokaryota, Protozoa, terrestrial. INTRODUCTION Article 10b of the CBD calls for signatories to ‘Adopt The original brief for this chapter was to review New Zealand’s measures relating to the use of biological resources [i.e. genetic genetic resources. The OECD defi nition of genetic resources resources] to avoid or minimize adverse impacts on biological is ‘genetic material of plants, animals or micro-organisms of diversity [e.g. genetic diversity]’ (my parentheses). -
Phylogeny and Classification of the Melastomataceae and Memecylaceae
Nord. J. Bot. - Section of tropical taxonomy Phylogeny and classification of the Melastomataceae and Memecy laceae Susanne S. Renner Renner, S. S. 1993. Phylogeny and classification of the Melastomataceae and Memecy- laceae. - Nord. J. Bot. 13: 519-540. Copenhagen. ISSN 0107-055X. A systematic analysis of the Melastomataceae, a pantropical family of about 4200- 4500 species in c. 166 genera, and their traditional allies, the Memecylaceae, with c. 430 species in six genera, suggests a phylogeny in which there are two major lineages in the Melastomataceae and a clearly distinct Memecylaceae. Melastomataceae have close affinities with Crypteroniaceae and Lythraceae, while Memecylaceae seem closer to Myrtaceae, all of which were considered as possible outgroups, but sister group relationships in this plexus could not be resolved. Based on an analysis of all morph- ological and anatomical characters useful for higher level grouping in the Melastoma- taceae and Memecylaceae a cladistic analysis of the evolutionary relationships of the tribes of the Melastomataceae was performed, employing part of the ingroup as outgroup. Using 7 of the 21 characters scored for all genera, the maximum parsimony program PAUP in an exhaustive search found four 8-step trees with a consistency index of 0.86. Because of the limited number of characters used and the uncertain monophyly of some of the tribes, however, all presented phylogenetic hypotheses are weak. A synapomorphy of the Memecylaceae is the presence of a dorsal terpenoid-producing connective gland, a synapomorphy of the Melastomataceae is the perfectly acrodro- mous leaf venation. Within the Melastomataceae, a basal monophyletic group consists of the Kibessioideae (Prernandra) characterized by fiber tracheids, radially and axially included phloem, and median-parietal placentation (placentas along the mid-veins of the locule walls). -
Projeto De Pesquisa
INSTITUTO DE PESQUISAS JARDIM BOTÂNICO DO RIO DE JANEIRO DIRETORIA DE PESQUISA CIENTÍFICA PROGRAMA INSTITUCIONAL DE BOLSAS DE INICIAÇÃO CIENTÍFICA (PIBIC/CNPq) PROJETO DE PESQUISA ESTUDOS MULTIDISCIPLINARES EM MELASTOMATACEAE NEOTROPICAIS: TAXONOMIA, FLORÍSTICA, ANATOMIA E ONTOGENIA Dr. José Fernando A. Baumgratz (orientador proponente) PLANOS DE TRABALHO (1) VASCULARIZAÇÃO E ONTOGENIA DE FLORES POLISTÊMONES EM MICONIA (MELASTOMATACEAE; MICONIEAE) (2) DIVERSIDADE DE MELASTOMATACEAE NO PARQUE NACIONAL DA SERRA DOS ÓRGÃOS, RIO DE JANEIRO, BRASIL Rio de Janeiro 2018 1 PROJETO DE PESQUISA ESTUDOS MULTIDISCIPLINARES EM MELASTOMATACEAE NEOTROPICAIS: TAXONOMIA, FLORÍSTICA E ANATOMIA INTRODUÇÃO A família Melastomataceae é uma das mais numerosas entre as Angiospermae, com 150 gêneros e em torno de 4.500 espécies (Renner et al. 2010), sendo floristicamente abundante e diversificada na América do Sul. A expressiva diversidade dessa família na flora brasileira está seguramente registrada na lista de plantas do Brasil recentemente divulgada, onde vários taxonomistas especialistas atestaram a validade dos táxons que a compõe (Baumgratz et al. 2010). No contexto nacional, representa a sexta maior família entre as Angiospermae, com 68 gêneros e mais de 1.300 espécies, sendo 845 endêmicas, e distribuindo-se desde a Amazônia e o centro-oeste até o Rio Grande do Sul e praticamente em todas as formações vegetacionais, exceto na Caatinga sensu stricto (Baumgratz & Souza 2005; Baumgratz et al. 2006, 2007). Entretanto, de acordo com Goldenberg et al. (2012), o número de gêneros poderá cair para 65, com base em estudos filogenéticos recentemente desenvolvidos, como os de Penneys et al. (2010) e Penneys & Judd (2011), que predizem alguns como sinônimos. De modo geral, a base do conhecimento sobre as Melastomataceae no Brasil ainda são as clássicas monografias publicadas no final do século XIX por Cogniaux (1883- 1888, 1891). -
Systematics and Relationships of Tryssophyton (Melastomataceae
A peer-reviewed open-access journal PhytoKeys 136: 1–21 (2019)Systematics and relationships of Tryssophyton (Melastomataceae) 1 doi: 10.3897/phytokeys.136.38558 RESEARCH ARTICLE http://phytokeys.pensoft.net Launched to accelerate biodiversity research Systematics and relationships of Tryssophyton (Melastomataceae), with a second species from the Pakaraima Mountains of Guyana Kenneth J. Wurdack1, Fabián A. Michelangeli2 1 Department of Botany, MRC-166 National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, DC 20013-7012, USA 2 The New York Botanical Garden, 2900 Southern Blvd., Bronx, NY 10458, USA Corresponding author: Kenneth J. Wurdack ([email protected]) Academic editor: Ricardo Kriebel | Received 25 July 2019 | Accepted 30 October 2019 | Published 10 December 2019 Citation: Wurdack KJ, Michelangeli FA (2019) Systematics and relationships of Tryssophyton (Melastomataceae), with a second species from the Pakaraima Mountains of Guyana. PhytoKeys 136: 1–21. https://doi.org/10.3897/ phytokeys.136.38558 Abstract The systematics of Tryssophyton, herbs endemic to the Pakaraima Mountains of western Guyana, is re- viewed and Tryssophyton quadrifolius K.Wurdack & Michelang., sp. nov. from the summit of Kamakusa Mountain is described as the second species in the genus. The new species is distinguished from its closest relative, Tryssophyton merumense, by striking vegetative differences, including number of leaves per stem and leaf architecture. A phylogenetic analysis of sequence data from three plastid loci and Melastomata- ceae-wide taxon sampling is presented. The two species of Tryssophyton are recovered as monophyletic and associated with mostly Old World tribe Sonerileae. Fruit, seed and leaf morphology are described for the first time, biogeography is discussed and both species are illustrated. -
Recommendation of Native Species for the Reforestation of Degraded Land Using Live Staking in Antioquia and Caldas’ Departments (Colombia)
UNIVERSITÀ DEGLI STUDI DI PADOVA Department of Land, Environment Agriculture and Forestry Second Cycle Degree (MSc) in Forest Science Recommendation of native species for the reforestation of degraded land using live staking in Antioquia and Caldas’ Departments (Colombia) Supervisor Prof. Lorenzo Marini Co-supervisor Prof. Jaime Polanía Vorenberg Submitted by Alicia Pardo Moy Student N. 1218558 2019/2020 Summary Although Colombia is one of the countries with the greatest biodiversity in the world, it has many degraded areas due to agricultural and mining practices that have been carried out in recent decades. The high Andean forests are especially vulnerable to this type of soil erosion. The corporate purpose of ‘Reforestadora El Guásimo S.A.S.’ is to use wood from its plantations, but it also follows the parameters of the Forest Stewardship Council (FSC). For this reason, it carries out reforestation activities and programs and, very particularly, it is interested in carrying out ecological restoration processes in some critical sites. The study area is located between 2000 and 2750 masl and is considered a low Andean humid forest (bmh-MB). The average annual precipitation rate is 2057 mm and the average temperature is around 11 ºC. The soil has a sandy loam texture with low pH, which limits the amount of nutrients it can absorb. FAO (2014) suggests that around 10 genera are enough for a proper restoration. After a bibliographic revision, the genera chosen were Alchornea, Billia, Ficus, Inga, Meriania, Miconia, Ocotea, Protium, Prunus, Psidium, Symplocos, Tibouchina, and Weinmannia. Two inventories from 2013 and 2019, helped to determine different biodiversity indexes to check the survival of different species and to suggest the adequate characteristics of the individuals for a successful vegetative stakes reforestation. -
Morphoanatomical Study of Clidemia Hirta (L.) D. Don. Estudo Morfoanatômico De Clidemia Hirta (L.) D
Research, Society and Development, v. 10, n. 7, e1310716159, 2021 (CC BY 4.0) | ISSN 2525-3409 | DOI: http://dx.doi.org/10.33448/rsd-v10i7.16159 Morphoanatomical study of Clidemia hirta (L.) D. Don. Estudo morfoanatômico de Clidemia hirta (L.) D. Don. Estudio morfoanatómico de Clidemia hirta (L.) D. Don. Received: 05/16/2021 | Reviewed: 05/25/2021 | Accept: 05/26/2021 | Published: 06/11/2021 Tatiane Mendonça da Silva ORCID: https://orcid.org/0000-0002-3553-901X Universidade Federal de Goiás, Brazil E-mail: [email protected] Heleno Dias Ferreira ORCID: https://orcid.org/0000-0001-7763-734X Universidade Federal de Goiás, Brazil E-mail: [email protected] José Realino de Paula ORCID: https://orcid.org/0000-0002-4424-7692 Universidade Federal de Goiás, Brazil E-mail: [email protected] Tatiana de Sousa Fiuza ORCID: https://orcid.org/0000-0003-0135-177X Universidade Federal de Goiás, Brazil E-mail: [email protected] Abstract The aims of this study were: to carry out the morphological study of the Clidemia hirta (L.) D. Don, the anatomical study of the leaves and young stem and the phytochemical screening of the powder of the leaves. The leaves were collected monthly at Bosque Auguste de Saint-Hilaire, Conservation Unit on Campus II of the Federal University of Goiás (UFG), Goiânia, Goiás, for 12 months. The specie was identified and a voucher specime deposited in the Herbarium of UFG (66 872- UFG). Morphoanatomical analysis was performed according to conventional techniques. It was verified at phytochemical screening, the presence de anthraquinone heterosides, starch, alkaloids, flavonoid and saponins. -
Review and Status of Biological Control of Clidemia in Hawaici
REVIEW AND STATUS OF BIOLOGICAL CONTROL OF CLIDEMIA IN HAWAICI Larry M. Nakahara, Robert Me Burkhart, and George Ye Funasaki ABSTRACT Efforts to control clidemia (Clidemia hirta) in Hawai'i with phytophagous insects began in 1952. Several attempts have been made since then to introduce potential biological control agents to reduce the spread of this weed into forest areas, and other control measures have been tried by various groups and agencies. It was not until recently, however, through the enactment of significant legislation and subsequent funding, that explorations and studies were conducted specifically on clidemia insects in Trinidad, West Indies. Fourteen species of insects were evaluated, including Carposina bullata, Mompha bithalama, a midge or cecidomyiid, two Eurytoma species, Piesmopoda sp., and Compsolechia seductella, which feed on the flowers and fruits; Lius poseidon, Antiblemma acclinalis, Druentia sp., prob. inscita, Ategumia matutinalis (formerly Blepharomastix ebulealis but originally thought to be Sylepte matutinalis), Penestes n. sp., and a leaf beetle or chrysomelid, which feed on the leaves; and a long-horned cerambycid beetle, which bores into the stem. Studies indicated that several species were sufficiently host specific to warrant introduction into Hawai'i for the biological control of clidemia. INTRODUCTION In Hawai'i, clidemia or Koster's curse (Clidemia hirta) (Melastomataceae), a fast-growing, hea -seeding, tropical American shrub, has colonized forest clearings, trailsi7 es, and bum sites and intruded into the understories of forests that were formerly free of introduced, or alien, weeds (Wester and Wood 1977). The species has spread rapidly throughout the State and re resents a serious threat to our native forests. -
The Evolution of Bat Pollination: a Phylogenetic Perspective
Annals of Botany 104: 1017–1043, 2009 doi:10.1093/aob/mcp197, available online at www.aob.oxfordjournals.org INVITED REVIEW The evolution of bat pollination: a phylogenetic perspective Theodore H. Fleming1,*, Cullen Geiselman2 and W. John Kress3 1Emeritus, Department of Biology, University of Miami, Coral Gables, FL 33124, USA, 2Institute of Systematic Botany, The New York Botanical Garden, Bronx, NY 10458, USA and 3Department of Botany, MRC-166, National Museum of Natural History, Smithsonian Institution, PO Box 37012, Washington, DC 20013-7012, USA Received: 2 April 2009 Returned for revision: 27 May 2009 Accepted: 13 July 2009 Published electronically: 29 September 2009 † Background Most tropical and subtropical plants are biotically pollinated, and insects are the major pollinators. A small but ecologically and economically important group of plants classified in 28 orders, 67 families and about 528 species of angiosperms are pollinated by nectar-feeding bats. From a phylogenetic perspective this is a derived pollination mode involving a relatively large and energetically expensive pollinator. Here its ecologi- cal and evolutionary consequences are explored. Downloaded from † Scope and Conclusions This review summarizes adaptations in bats and plants that facilitate this interaction and discusses the evolution of bat pollination from a plant phylogenetic perspective. Two families of bats contain specialized flower visitors, one in the Old World and one in the New World. Adaptation to pollination by bats has evolved independently many times from a variety of ancestral conditions, including insect-, bird- and non-volant mammal-pollination. Bat pollination predominates in very few families but is relatively common in certain angiosperm subfamilies and tribes. -
Elatinaceae Are Sister to Malpighiaceae; Peridiscaceae Belong to Saxifragales
Elatinaceae are Sister to Malpighiaceae; Peridiscaceae Belong to Saxifragales The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Davis, Charles C., and Mark W. Chase. 2004. Elatinaceae are sister to Malpighiaceae; Peridiscaceae belong to Saxifragales. American Journal of Botany 91(2): 262-273. Published Version http://dx.doi.org/10.3732/ajb.91.2.262 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:2666728 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA American Journal of Botany 91(2): 262±273. 2004. ELATINACEAE ARE SISTER TO MALPIGHIACEAE; PERIDISCACEAE BELONG TO SAXIFRAGALES1 CHARLES C. DAVIS2,4 AND MARK W. C HASE3 2Department of Ecology and Evolutionary Biology, University of Michigan Herbarium, 3600 Varsity Drive, Ann Arbor, Michigan 48108-2287 USA; and 3Molecular Systematics Section, Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS UK Phylogenetic data from plastid (ndhF and rbcL) and nuclear (PHYC) genes indicate that, within the order Malpighiales, Elatinaceae are strongly supported as sister to Malpighiaceae. There are several putative morphological synapomorphies for this clade; most notably, they both have a base chromosome number of X 5 6 (or some multiple of three or six), opposite or whorled leaves with stipules, unicellular hairs (also uniseriate in some Elatinaceae), multicellular glands on the leaves, and resin (Elatinacae) or latex (Malpighiaceae). -
Clidemia Hirta (L.) D
Crop Protection Compendium - Clidemia hirta (L.) D. Don Pierre Binggeli 2005 NAMES AND TAXONOMY Preferred scientific name Clidemia hirta (L.) D. Don Taxonomic position Other scientific names Domain: Eukaryota Melastoma hirta sensu Miller Kingdom: Viridiplantae Melastoma hirtum L. Phylum: Spermatophyta Clidemia crenata DC. Subphylum: Angiospermae Melastoma elegans Aublet Class: Dicotyledonae Clidemia elegans (Aublet) D. Don Order: Myrtales Melastoma hirta L. Family: Melastomataceae BAYER code CXAHI (Clidemia hirta) Common names English: Belau: Madagascar: Koster's curse kui manzana soap bush kúi mazambôdy curse Fiji: Martinique: Spanish: Koster's curse bonbon bleu camasey bona na bulamakau herbe à cré cré camasey peludo kaurasinga Portugal: nigua kauresinga caiuia sietecueros mara na bulumakau pixirica French: mbona na mbulamakau Samoa: canot-macaque ndraunisinga la'au lau mamoe herbe-côtelletes roinisinga Singapore: herbecrécré vuti hairy Clidemia Mélastome élégant Haiti: Mélastome poilu guéri vite Notes on taxonomy and nomenclature Varieties of C. hirta have been described. Var. hirta and var. elegans were introduced to Hawaii and the Seychelles, respectively. Binggeli 2005 Crop Protection Compendium - Clidemia hirta (L.) D. Don 1 HOST RANGE Major hosts Cocos nucifera (coconut), Hevea brasiliensis (rubber), Theobroma cacao (cocoa) Minor hosts pastures HABITAT Most tropical island forest areas appear to be susceptible to C. hirta invasion regardless of their floristic composition, as long as some form of disturbance affects them. In Hawaii all new instances of C. hirta occur in disturbed areas such as roadsides and landslides and following disturbance by windstorm, pigs, landslides and fire. In the East Usambaras (Tanzania) the shrub is found not only along roadsides but also in many parts of the undisturbed montane forest (Binggeli, 2003). -
Additions to the Flora of Panama, with Comments on Plant Collections and Information Gaps
15 4 NOTES ON GEOGRAPHIC DISTRIBUTION Check List 15 (4): 601–627 https://doi.org/10.15560/15.4.601 Additions to the flora of Panama, with comments on plant collections and information gaps Orlando O. Ortiz1, Rodolfo Flores2, Gordon McPherson3, Juan F. Carrión4, Ernesto Campos-Pineda5, Riccardo M. Baldini6 1 Herbario PMA, Universidad de Panamá, Vía Simón Bolívar, Panama City, Panama Province, Estafeta Universitaria, Panama. 2 Programa de Maestría en Biología Vegetal, Universidad Autónoma de Chiriquí, El Cabrero, David City, Chiriquí Province, Panama. 3 Herbarium, Missouri Botanical Garden, 4500 Shaw Boulevard, St. Louis, Missouri, MO 63166-0299, USA. 4 Programa de Pós-Graduação em Botânica, Universidade Estadual de Feira de Santana, Avenida Transnordestina s/n, Novo Horizonte, 44036-900, Feira de Santana, Bahia, Brazil. 5 Smithsonian Tropical Research Institute, Luis Clement Avenue (Ancón, Tupper 401), Panama City, Panama Province, Panama. 6 Centro Studi Erbario Tropicale (FT herbarium) and Dipartimento di Biologia, Università di Firenze, Via La Pira 4, 50121, Firenze, Italy. Corresponding author: Orlando O. Ortiz, [email protected]. Abstract In the present study, we report 46 new records of vascular plants species from Panama. The species belong to the fol- lowing families: Anacardiaceae, Apocynaceae, Aquifoliaceae, Araceae, Bignoniaceae, Burseraceae, Caryocaraceae, Celastraceae, Chrysobalanaceae, Cucurbitaceae, Erythroxylaceae, Euphorbiaceae, Fabaceae, Gentianaceae, Laciste- mataceae, Lauraceae, Malpighiaceae, Malvaceae, Marattiaceae, Melastomataceae, Moraceae, Myrtaceae, Ochnaceae, Orchidaceae, Passifloraceae, Peraceae, Poaceae, Portulacaceae, Ranunculaceae, Salicaceae, Sapindaceae, Sapotaceae, Solanaceae, and Violaceae. Additionally, the status of plant collections in Panama is discussed; we focused on the areas where we identified significant information gaps regarding real assessments of plant biodiversity in the country.