The Importance of Livelihood Strategy and Ethnicity
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NUMBERED TREE SPECIES LIST in SOUTH AFRICA CYATHEACEAE 1 Cyathea Dregei 2 Cyathea Capensis Var. Capensis ZAMIACEAE 3 Encephalart
NUMBERED TREE SPECIES LIST IN SOUTH AFRICA 23 Hyphaene coriacea CYATHEACEAE 24 Hyphaene petersiana 1 Cyathea dregei 25 Borassus aethiopum 2 Cyathea capensis var. capensis 26 Raphia australis 27 Jubaeopsis caffra ZAMIACEAE 3 Encephalartos altensteinii ASPHODELACEAE 3.1 Encephalartos eugene-maraisii 28 Aloe barberae 3.2 Encephalartos arenarius 28.1 Aloe arborescens 3.3 Encephalartos brevifoliolatus 28.2 Aloe africana 3.4 Encephalartos ferox 28.3 Aloe alooides 4 Encephalartos friderici-guilielmi 28.4 Aloe angelica 5 Encephalartos ghellinckii 28.5 Aloe candelabrum 5.1 Encephalartos inopinus 28.6 Aloe castanea 5.2 Encephalartos lanatus 28.7 Aloe comosa 6 Encephalartos laevifolius 28.8 Aloe excelsa var. excelsa 7 Encephalartos latifrons 29 Aloe dichotoma 8 Encephalartos senticosus 29.1 Aloe dolomitica 8.1 Encephalartos lehmannii 29.2 Aloe ferox 9 Encephalartos longifolius 29.3 Aloe khamiesensis 10 Encephalartos natalensis 29.4 Aloe littoralis 11 Encephalartos paucidentatus 29.5 Aloe marlothii subsp. marlothii 12 Encephalartos princeps 29.6 Aloe plicatilis 12.5 Encephalartos relictus 29.7 Aloe marlothii subsp. orientalis 13 Encephalartos transvenosus 30 Aloe pillansii 14 Encephalartos woodii 30.1 Aloe pluridens 14.1 Encephalartos heenanii 30.2 Aloe ramosissima 14.2 Encephalartos dyerianus 30.3 Aloe rupestris 14.3 Encephalartos middelburgensis 30.4 Aloe spicata 14.4 Encephalartos dolomiticus 30.5 Aloe speciosa 14.5 Encephalartos aemulans 30.6 Aloe spectabilis 14.6 Encephalartos hirsutus 30.7 Aloe thraskii 14.7 Encephalartos msinganus 14.8 Encephalartos -
Chapter One 1.0 Introduction and Background to The
CHAPTER ONE 1.0 INTRODUCTION AND BACKGROUND TO THE STUDY Loganiaceae is a family of flowering plants classified in the Order Gentianales (Bendre, 1975). The family was first suggested by Robert Brown in 1814 and validly published by von Martius in 1827 (Nicholas and Baijnath, 1994). Members habits are in form of trees, shrubs, woody climbers and herbs. Some are epiphytes while some members are furnished with spines or tendrils (Bendre, 1975). They are distributed mainly in the tropics, subtropics and a few in temperate regions (Backlund et al., 2000). Earlier treatments of the family have included up to 30 genera, 600 species (Leeuwenberg and Leenhouts, 1980; Mabberley, 1997) but were later reduced to 400 species in 15 genera, with some species extending into temperate Australia and North America (Struwe et al., 1994; Dunlop, 1996; Backlund and Bremer, 1998). Morphological studies have demonstrated that this broadly defined Loganiaceae was a polyphyletic assemblage and numerous genera have been removed from it to other families (sometimes to other Orders), e.g. Gentianaceae, Gelsemiaceae, Plocospermataceae, Tetrachondraceae, Buddlejaceae, and Gesneriaceae (Backlund and Bremer, 1998; Backlund et al., 2000). The family has undergone numerous revisions that have expanded and contracted its circumscription, ranging from one genus at its smallest (Takhtajan, 1997; Smith et al., 1997) to 30 at its largest (Leeuwenberg and Leenhouts, 1980). One of the current infrafamilial classifications contains four tribes: Antonieae Endl., Loganieae Endl., Spigelieae Dum. (monotypic), and Strychneae Dum. (Struwe et al., 1994). The tribes Loganieae and Antonieae are supported by molecular data, but Strychneae is not (Backlund et al., 2000). -
SABONET Report No 18
ii Quick Guide This book is divided into two sections: the first part provides descriptions of some common trees and shrubs of Botswana, and the second is the complete checklist. The scientific names of the families, genera, and species are arranged alphabetically. Vernacular names are also arranged alphabetically, starting with Setswana and followed by English. Setswana names are separated by a semi-colon from English names. A glossary at the end of the book defines botanical terms used in the text. Species that are listed in the Red Data List for Botswana are indicated by an ® preceding the name. The letters N, SW, and SE indicate the distribution of the species within Botswana according to the Flora zambesiaca geographical regions. Flora zambesiaca regions used in the checklist. Administrative District FZ geographical region Central District SE & N Chobe District N Ghanzi District SW Kgalagadi District SW Kgatleng District SE Kweneng District SW & SE Ngamiland District N North East District N South East District SE Southern District SW & SE N CHOBE DISTRICT NGAMILAND DISTRICT ZIMBABWE NAMIBIA NORTH EAST DISTRICT CENTRAL DISTRICT GHANZI DISTRICT KWENENG DISTRICT KGATLENG KGALAGADI DISTRICT DISTRICT SOUTHERN SOUTH EAST DISTRICT DISTRICT SOUTH AFRICA 0 Kilometres 400 i ii Trees of Botswana: names and distribution Moffat P. Setshogo & Fanie Venter iii Recommended citation format SETSHOGO, M.P. & VENTER, F. 2003. Trees of Botswana: names and distribution. Southern African Botanical Diversity Network Report No. 18. Pretoria. Produced by University of Botswana Herbarium Private Bag UB00704 Gaborone Tel: (267) 355 2602 Fax: (267) 318 5097 E-mail: [email protected] Published by Southern African Botanical Diversity Network (SABONET), c/o National Botanical Institute, Private Bag X101, 0001 Pretoria and University of Botswana Herbarium, Private Bag UB00704, Gaborone. -
Albany Thicket Biome
% S % 19 (2006) Albany Thicket Biome 10 David B. Hoare, Ladislav Mucina, Michael C. Rutherford, Jan H.J. Vlok, Doug I.W. Euston-Brown, Anthony R. Palmer, Leslie W. Powrie, Richard G. Lechmere-Oertel, Şerban M. Procheş, Anthony P. Dold and Robert A. Ward Table of Contents 1 Introduction: Delimitation and Global Perspective 542 2 Major Vegetation Patterns 544 3 Ecology: Climate, Geology, Soils and Natural Processes 544 3.1 Climate 544 3.2 Geology and Soils 545 3.3 Natural Processes 546 4 Origins and Biogeography 547 4.1 Origins of the Albany Thicket Biome 547 4.2 Biogeography 548 5 Land Use History 548 6 Current Status, Threats and Actions 549 7 Further Research 550 8 Descriptions of Vegetation Units 550 9 Credits 565 10 References 565 List of Vegetation Units AT 1 Southern Cape Valley Thicket 550 AT 2 Gamka Thicket 551 AT 3 Groot Thicket 552 AT 4 Gamtoos Thicket 553 AT 5 Sundays Noorsveld 555 AT 6 Sundays Thicket 556 AT 7 Coega Bontveld 557 AT 8 Kowie Thicket 558 AT 9 Albany Coastal Belt 559 AT 10 Great Fish Noorsveld 560 AT 11 Great Fish Thicket 561 AT 12 Buffels Thicket 562 AT 13 Eastern Cape Escarpment Thicket 563 AT 14 Camdebo Escarpment Thicket 563 Figure 10.1 AT 8 Kowie Thicket: Kowie River meandering in the Waters Meeting Nature Reserve near Bathurst (Eastern Cape), surrounded by dense thickets dominated by succulent Euphorbia trees (on steep slopes and subkrantz positions) and by dry-forest habitats housing patches of FOz 6 Southern Coastal Forest lower down close to the river. -
THE LOGANIACEAE of AFRICA XIV a Revision of Nuxia Lam
582.935.4:581.4/.S +581.9(6) MEDEDELINGEN LANDBOUWHOGESCHOOL WAGENINGEN • NEDERLAND • 75-8 (1975) THE LOGANIACEAE OF AFRICA XIV A revision ofNuxi a Lam. A. J. M. LEEUWENBERG Laboratory of Plant Taxonomy andPlant Geography, Agricultural University, Wageningen, The Netherlands (Received 24-111-1975) Published 19-VIII197 5 INTRODUCTION The present publication is a revision on a monographic basis of the genus Nuxia. The genus is restricted to Africa where the present author had theop portunity to study the most variable species, N. congesta, in the field in two dif ferent countries, viz. Cameroun and Ivory Coast. Fortunately most herbarium specimens proved to be well preserved and richly flowering or fruiting. HISTORY OF THE GENUS LA.MA.RCK (1791) founded the genus Nuxia on the basis of a single species, N.verticillata. PERSOON (1805) placed it in LINNAEUS'S Tetrandria monogynia, afterwards RAFINESQUE (1820) near Rondeletia in the Ixorineae of the Rubia- ceae, then REICHENBACH (1828) gave it a place in the Verbenaceae. Meanwhile R. BROWN (1814) named the second species N. congesta which was discovered in Ethiopia and was described only in 1838b y FRESENIUS. BENTHAM (1836) moved Nuxia to thetrib e Buddlejeae of the Scrophulariaceae and added some more species. Only one of them, however, N.floribunda, is maintained here in this genus. All the others belong to Buddleja according to, e.g., Miss I.C . VERDOORN (1958) andth epresen t author. BENTHAM was followed by MEISNER (1840), ENDLICHER (1841), REICHENBACH (1841), and KUNTH (1846), placing Nuxia there. Independently from BENTHAM, HOCHSTETTER (1843) described the new genus Lachnopylis in theLoganiaceae, based on two species, L. -
Zimbabwe-Mozambique)
A peer-reviewed open-access journal PhytoKeys 145: 93–129 (2020) Plant checklist for the Bvumba Mountains 93 doi: 10.3897/phytokeys.145.49257 RESEARCH ARTICLE http://phytokeys.pensoft.net Launched to accelerate biodiversity research Mountains of the Mist: A first plant checklist for the Bvumba Mountains, Manica Highlands (Zimbabwe-Mozambique) Jonathan Timberlake1, Petra Ballings2,3, João de Deus Vidal Jr4, Bart Wursten2, Mark Hyde2, Anthony Mapaura4,5, Susan Childes6, Meg Coates Palgrave2, Vincent Ralph Clark4 1 Biodiversity Foundation for Africa, 30 Warren Lane, East Dean, E. Sussex, BN20 0EW, UK 2 Flora of Zimbabwe & Flora of Mozambique projects, 29 Harry Pichanick Drive, Alexandra Park, Harare, Zimbabwe 3 Meise Botanic Garden, Bouchout Domain, Nieuwelaan 38, 1860, Meise, Belgium 4 Afromontane Research Unit & Department of Geography, University of the Free State, Phuthaditjhaba, South Africa 5 National Her- barium of Zimbabwe, Box A889, Avondale, Harare, Zimbabwe 6 Box BW53 Borrowdale, Harare, Zimbabwe Corresponding author: Vincent Ralph Clark ([email protected]) Academic editor: R. Riina | Received 10 December 2019 | Accepted 18 February 2020 | Published 10 April 2020 Citation: Timberlake J, Ballings P, Vidal Jr JD, Wursten B, Hyde M, Mapaura A, Childes S, Palgrave MC, Clark VR (2020) Mountains of the Mist: A first plant checklist for the Bvumba Mountains, Manica Highlands (Zimbabwe- Mozambique). PhytoKeys 145: 93–129. https://doi.org/10.3897/phytokeys.145.49257 Abstract The first comprehensive plant checklist for the Bvumba massif, situated in the Manica Highlands along the Zimbabwe-Mozambique border, is presented. Although covering only 276 km2, the flora is rich with 1250 taxa (1127 native taxa and 123 naturalised introductions). -
An Annotated Checklist to the Trees and Shrubs of the Upper Katanga (D.R
Phytotaxa 258 (3): 201–250 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2016 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.258.3.1 An annotated checklist to the trees and shrubs of the Upper Katanga (D.R. Congo) PIERRE MEERTS Herbarium et Bibliothèque de botanique africaine, Université Libre de Bruxelles, Campus de la Plaine, Boulevard du Triomphe, CP 265, B-1050 Brussels, Belgium; [email protected] Abstract A checklist to the trees and shrubs of Upper Katanga (the Zambezian part of Katanga, ca. 260,000 km²) (D.R. Congo) is presented. It comprises 694 taxa (664 species, 15 subspecies, 15 varieties). For each accepted taxon the list provides habitat and geographic distribution. Eleven taxa are new records for the D.R. Congo and 29 are new records for Upper Katanga. Fourteen new synonyms are proposed. Two families stand out as particularly species-rich, i.e. Fabaceae (110 taxa, i.e. Cae- salpinioideae: 50; Faboideae: 29; Mimosoideae: 31) and Rubiaceae (74). Six genera comprise 10 taxa or more i.e. Ficus (25), Combretum (17), Monotes (17), Brachystegia (15), Diospyros (11), Acacia (11). The three most important woody vegetation types in Upper Katanga have different phytogeographic and taxonomic assemblages: miombo woodland (254 taxa, 62% of which are Zambezian, over-representation of Caesalpinioideae), riverine and swamp forest (196 taxa, 36% of which are Guineo-Congolian, 17% Afromontane), and Zambezian dry evergreen forest (117 taxa, 37% of which are Guineo-Congo- lian, Rubiaceae over-represented). Twenty taxa (3%) are strictly endemic to Upper Katanga, most of which occur only in the Katango-Zambian sector of the Zambezian region. -
Bioprospecting the Flora of Southern Africa: Optimising Plant Selections
Bioprospecting the flora of southern Africa: optimising plant selections Dissertation for Master of Science Errol Douwes 2005 Submitted in fulfilment of the requirements for the degree of Master of Science in the School of Biological and Conservation Sciences at the University of KwaZulu-Natal Pietermaritzburg, South Africa ii Preface The work described in this dissertation was carried out at the Ethnobotany Unit, South African National Biodiversity Institute, Durban and at the School of Biological and Conservation Sciences, University of KwaZulu-Natal, Pietermaritzburg from January 2004 to November 2005 under the supervision of Professor TJ. Edwards (School of Biological and Conservation Sciences, University of KwaZulu-Natal, Pietermaritzburg) and Dr N. R. Crouch (Ethnobotany Unit, South African National Biodiversity Institute, Durban). These studies, submitted for the degree of Master of Science in the School of Biological and Conservation Sciences, University of KwaZulu-Natal, Pietermaritzburg, represent the original work of the author and have not been submitted in any form to another university. Use of the work of others has been duly acknowledged in the text. We certify that the above statement is correct Novem:RE. Douwes Professor T.J. Edwards /JIo-~rA ..............................~ ...~ Dr N.R. Crouch iii Acknowledgements Sincere thanks are due to my supervisors Prof. Trevor Edwards and Dr Neil Crouch for their guidance and enthusiasm in helping me undertake this project. Dr Neil Crouch is thanked for financial support provided by way of SANSI (South African National Siodiversity Institute) and the NDDP (Novel Drug Development Platform). Prof. Trevor Edwards and Prof. Dulcie Mulholland are thanked for financial support provided by way of NRF (National Research Foundation) grant-holder bursaries. -
Savanna Fire and the Origins of the “Underground Forests” of Africa
SAVANNA FIRE AND THE ORIGINS OF THE “UNDERGROUND FORESTS” OF AFRICA Olivier Maurin1, *, T. Jonathan Davies1, 2, *, John E. Burrows3, 4, Barnabas H. Daru1, Kowiyou Yessoufou1, 5, A. Muthama Muasya6, Michelle van der Bank1 and William J. Bond6, 7 1African Centre for DNA Barcoding, Department of Botany & Plant Biotechnology, University of Johannesburg, PO Box 524 Auckland Park 2006, Johannesburg, Gauteng, South Africa; 2Department of Biology, McGill University, 1205 ave Docteur Penfield, Montreal, QC H3A 0G4, Quebec, Canada; 3Buffelskloof Herbarium, P.O. Box 710, Lydenburg, 1120, South Africa; 4Department of Plant Sciences, University of Pretoria, Private Bag X20 Hatfield 0028, Pretoria, South Africa; 5Department of Environmental Sciences, University of South Africa, Florida campus, Florida 1710, Gauteng, South Africa; 6Department of Biological Sciences and 7South African Environmental Observation Network, University of Cape Town, Rondebosch, 7701, Western Cape, South Africa *These authors contributed equally to the study Author for correspondence: T. Jonathan Davies Tel: +1 514 398 8885 Email: [email protected] Manuscript information: 5272 words (Introduction = 1242 words, Materials and Methods = 1578 words, Results = 548 words, Discussion = 1627 words, Conclusion = 205 words | 6 figures (5 color figures) | 2 Tables | 2 supporting information 1 SUMMARY 1. The origin of fire-adapted lineages is a long-standing question in ecology. Although phylogeny can provide a significant contribution to the ongoing debate, its use has been precluded by the lack of comprehensive DNA data. Here we focus on the ‘underground trees’ (= geoxyles) of southern Africa, one of the most distinctive growth forms characteristic of fire-prone savannas. 2. We placed geoxyles within the most comprehensive dated phylogeny for the regional flora comprising over 1400 woody species. -
Expanding the Reach: Ethnobotanical Knowledge and Technological Intensification in Beekeeping Among the Ogiek of the Mau Forest
Zocchi et al. Journal of Ethnobiology and Ethnomedicine (2020) 16:57 https://doi.org/10.1186/s13002-020-00409-w RESEARCH Open Access Expanding the reach: ethnobotanical knowledge and technological intensification in beekeeping among the Ogiek of the Mau Forest, Kenya Dauro Mattia Zocchi1, Gabriele Volpato1, Duncan Chalo2, Patrick Mutiso2 and Michele Filippo Fontefrancesco1* Abstract Background: Initiatives for beekeeping intensification across the tropics can foster production and income, but the changes triggered by the introduction of modern beehives might permeate traditional knowledge and practices in multiple ways, and as such should be investigated and understood. We conducted an ethnobotanical study in the Eastern part of the Mau Forest among Ogiek beekeepers who customarily practice forest beekeeping and who are involved in a project aimed at the modernization of their beekeeping activities. We aimed to document the beekeeping-associated ethnobotanical knowledge, exploring the relationships and complementarity between modern and traditional knowledge and practices. Methods: Field research was carried out through semi-structured interviews with 30 Ogiek beekeepers and 10 additional stakeholders. We collected ethnobotanical data about plants used for beekeeping purposes, and ethnographic information on traditional and modern beekeeping systems. Results: We report 66 plant species, distributed across 36 botanical families representing 58 genera, important as melliferous, for the construction and placing of hives, attracting bees, and harvesting and storing honey. Dombeya torrida (J.F.Gmel.) Bamps, Juniperus procera Hochst.exEndl.,andPodocarpus latifolius (Thunb.) R.Br. ex Mirb. are the species with the most mentions and the highest number of uses. Our study reveals that the Ogiek possess a detailed knowledge of the forest’sflora, its importance and uses and that this knowledge underpins beekeeping practices. -
Observations of the Effects of Drought on Evergreen and Deciduous Species in the Eastern Cape Forests
522 S.Afr.J .Bot., 1993, 59(5): 522-534 Observations of the effects of drought on evergreen and deciduous species in the eastern Cape forests C.J. Geldenhuys CSIR Division of Forest Science and Technology, P.O. Box 395, Pretoria, 0001 Republic of South Africa Received 10 February 1993; revised 8 JUlie 1993 A study was initiated in the eastern Cape forests, just alter the severe drought which ended in July 1983. The relative importance, survival and recovery of deciduous and evergreen species were studied on seven sites which covered an environmental gradient between the East London coast and the inland Amatole mountain complex. Seventy tree species were recorded of which twelve were deciduous and eight semi-deciduous. The results show no relationship between percentage deciduousness and temperatu re (attitude), soil moisture (pH) or soil fertility (available phosphorus). The coastal and the lowland sites we re most adversely affected. Of the 236 trees which initially showed some drought impact, only 47 were dead after 40 months, and 45 of these had been evergreen trees. Leaves of most evergreen species died while they remained attached to the branches, including the rare endemic Umtiza listeriana. The evergreen Buxus macowanii in the coastal site was not affected by the drought, but was severely defoliated by a Pafpita species (Lepi doptera), after which some trees and most of the saplings died. Most deciduous and semi-deciduous trees were not affected by the drought, and flushed and flowered shortly after the first rains. There are slight indications of better growth in deciduous than in evergreen trees. -
S Tau D E Et a L. / M Etam Orphosis 31 (3 ): 1 – 38 0
Pyraloidea: Crambidae: Cybalomiinae, Evergestinae, Glaphyriinae, Odentiinae, Pyraustinae, Spilomelinae Date of Host species Locality collection (c), Ref. no. Lepidoptera species Rearer Final instar larva Adult (Family) pupation (p), emergence (e) Crambidae: Cybalomiinae M1213 Ptychopseustis sp. Capparis tomentosa Tshukudu Game Reserve; c 7.2.2016 A. & I. Sharp (det. D. Agassiz) (Capparaceae) Hoedspruit; p 18.2.2016 Limpopo; e 29.2.2016 South Africa Crambidae: Evergestinae QG021 Crocidolomia pavonana Capparis tomentosa Beacon Bay; c 1.5.2019 Q. Grobler (Capparaceae) East London; p 17.5.2019 Staude Eastern Cape; e 28.5.2019 South Africa et al . / Metamorphosis / Crambidae: Glaphyriinae M1301 Hellula undalis Cleome monophylla Casketts, farm; c 12.4.2016 A. & I. Sharp (Cleomaceae) Hoedspruit; p 17.4.2016 31 (3) Limpopo; e 23.4.2016 : South Africa 1 ‒ 380 M1889 Hellula undalis Raphanus raphanistrum York; c 19.10.2017 A. & I. Sharp (Brassicaceae) Hoedspruit; p ? Limpopo; e 26.10.2017 South Africa M2170 Hellula undalis Cleome monophylla York; c 19.5.2018 A. & I. Sharp (Cleomaceae) Hoedspruit; p 21.5.2018 Limpopo; e 2.6.2018 South Africa 345 Pyraloidea: Crambidae: Cybalomiinae, Evergestinae, Glaphyriinae, Odentiinae, Pyraustinae, Spilomelinae SM19_02 Hellula undalis Brassica oleracea Haarlem Street; c 15.4.2019 S. Mecenero (Brassicaceae) Somerset West; p 29.4.2019 Western Cape; e 6.5.2019 South Africa Crambidae: Odentiinae 17HSS62 Autocharis sinualis Combretum zeyheri Hartbeesfontein, farm; c 14.10.2017 H. S. Staude (Combretaceae) Hekpoort; p 27.10.2017 Gauteng; e 9.11.2017 South Africa M1400 Autocharis sp. Combretum York; c 7.10.2016 A. & I. Sharp (det. D. Agassiz) mossambicense Hoedspruit; p 18.10.2016 Staude (Combretaceae) Limpopo; e 30.10.2016 South Africa et al .