Protea May Predict Occurrence and Abundance Alan T.K
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South Africa Cape Wildflowers, Birding & Big Game II 21St August to 3Rd September 2022 (14 Days)
South Africa Cape Wildflowers, Birding & Big Game II 21st August to 3rd September 2022 (14 days) Cape Mountain Zebras & wildflowers in West Coast NP by Adam Riley This comprehensive tour covers the most exciting regions of the Cape in our quest to experience both breathtaking displays of wildflowers and to track down some of the country’s endemic birds. We begin in the vibrant city of Cape Town, where Table Mountain provides a spectacular backdrop to the immensely diverse fynbos that cloaks the cities periphery. This fynbos constitutes the Cape Floral Kingdom – the smallest and richest of the world’s 6 floral kingdoms. It is also the only floral kingdom to be confined to the boundaries of a single country. Thereafter we venture to the West Coast and Namaqualand, which boast an outrageous and world famous floral display in years of good rains, before travelling through the heart of the country’s semi-desert region, focusing on the special bird’s endemic to this ancient landscape. We conclude the journey heading out of wildflower country to Augrabies Falls, an area offering unparalleled raptor viewing and a wide range of dry region birds. We invite you on this celebration of some of the finest wildflower and endemic birding that the African continent has to offer! RBT South Africa - Cape Wildflowers, Birding & Big Game 2 THE TOUR AT A GLANCE… THE ITINERARY Day 1 Arrival in Upington Day 2 Upington to Augrabies Falls National Park Day 3 Augrabies Falls National Park Day 4 Augrabies Falls National Park to Springbok Day 5 Springbok to Nieuwoudtville -
Urbanization, Climate and Ecological Stress Indicators in an Endemic Nectarivore, the Cape Sugarbird
Urbanization, climate and ecological stress indicators in an endemic nectarivore, the Cape Sugarbird B. Mackay, A. T. K. Lee, P. Barnard, A. P. Møller & M. Brown Journal of Ornithology ISSN 2193-7192 J Ornithol DOI 10.1007/s10336-017-1460-9 1 23 Your article is protected by copyright and all rights are held exclusively by Dt. Ornithologen-Gesellschaft e.V.. This e-offprint is for personal use only and shall not be self- archived in electronic repositories. If you wish to self-archive your article, please use the accepted manuscript version for posting on your own website. You may further deposit the accepted manuscript version in any repository, provided it is only made publicly available 12 months after official publication or later and provided acknowledgement is given to the original source of publication and a link is inserted to the published article on Springer's website. The link must be accompanied by the following text: "The final publication is available at link.springer.com”. 1 23 Author's personal copy J Ornithol DOI 10.1007/s10336-017-1460-9 ORIGINAL ARTICLE Urbanization, climate and ecological stress indicators in an endemic nectarivore, the Cape Sugarbird 1 1,2 1,2 3 4,5 B. Mackay • A. T. K. Lee • P. Barnard • A. P. Møller • M. Brown Received: 10 February 2016 / Revised: 6 October 2016 / Accepted: 21 April 2017 Ó Dt. Ornithologen-Gesellschaft e.V. 2017 Abstract Stress, as a temporary defense mechanism urban settlements had higher levels of fluctuating asym- against specific stimuli, can place a bird in a state in which metry and fault bars in feathers. -
Pollination Structures Plant and Nectar‐Feeding Bird
Received: 10 April 2020 Revised: 22 April 2020 Accepted: 3 May 2020 DOI: 10.1111/1440-1703.12148 ORIGINAL ARTICLE Pollination structures plant and nectar-feeding bird communities in Cape fynbos, South Africa: Implications for the conservation of plant–bird mutualisms Sjirk Geerts1 | Anina Coetzee2 | Anthony G. Rebelo3 | Anton Pauw4 1Department Conservation and Marine Sciences, Cape Peninsula University of Abstract Technology, Cape Town, South Africa With the current global concerns about pollinators, relationships between spe- 2DST/NRF Centre of Excellence at the cies interactions and diversity are pivotal. If pollinator communities depend FitzPatrick Institute of African strongly on the diversity of flowering plants and vice versa, anthropogenic Ornithology, University of Cape Town, Cape Town, South Africa influences—whether positive or negative—on one partner will cause changes 3South African National Biodiversity in the other. Here we ask whether nectarivorous bird communities are struc- Institute, Kirstenbosch Research Centre, tured by resource abundance (Proteaceae nectar) or Proteaceae diversity at dif- Claremont, South Africa ferent spatial scales in the Cape fynbos of South Africa. On a small spatial 4Department of Botany and Zoology, Stellenbosch University, Matieland, scale, we sampled 34 one-hectare plots across the Cape Floristic Region (CFR) South Africa for flowering Proteaceae species, number of inflorescences, nectar volume, veg- etation age, nectar-feeding bird abundance and species richness. At small Correspondence Sjirk Geerts, Department Conservation scale, nectar—rather than vegetation structure or plant community and Marine Sciences, Cape Peninsula composition—was the most strongly correlated to nectar-feeding bird diversity University of Technology, P.O. Box and abundance. On a landscape scale we investigated the spatio-temporal 652, Cape Town 8000, South Africa. -
Newsletter Number 82 – December 2020
Affiliated to BirdLife South Africa Principal supporter of the Wakkerstroom Junior Bird Clubs NEWSLETTER NUMBER 82 – DECEMBER 2020 Hello fellow Birders, The Bird of the Year for 2021 has just been announced by BirdLife South Africa, which I thought is a good excuse to pop into your Inbox …. It’s the Cape Rockjumper Chaetops frenatus. What a stunning little bird to see! The photograph below is by Adam Riley. With red eyes and striking colouration, the Cape Rockjumper is one of South Africa’s most recognisable bird species. As it is restricted to the Fynbos Biome of South Africa, it is a major economic asset to the country, with birdwatchers from all over the world travelling here to see it, as well as the other endemic species restricted to the Cape Floral Kingdom. Together with its sister species, the Drakensberg Rockjumper, this bird family is restricted to South Africa and Lesotho. BirdLife South Africa chose this species as ‘Bird of the Year’ as it is an ambassador for the Fynbos biome: the unique plant kingdom found only in South Africa. There are seven other bird species found here and nowhere else on earth: Cape Sugarbird, Orange-breasted Sunbird, Protea Canary, Cape Siskin, Victorin’s Warbler, Agulhas Long-billed Lark and Hottentot Buttonquail. The Fynbos extends from the northern Cederberg through the Cape Fold Mountains, to Port Elizabeth, with fragments as far as Makhanda/Grahamstown. The Fynbos is generally well protected within the Cape Nature reserves of the Western Cape, but there are major concerns regarding the spread of alien tree species like pines and wattles, as well as increased fire frequencies as a result of climate change. -
NEST-SITE SELECTION in the CAPE SUGARBIRD We Dedicate
NEST-SITE SELECTION IN THE CAPE SUGARBIRD A. E. BURGER, W. R. SlEGFRIED & P. G. H. FROST Percy FitzPatrick Institute, University of Cape Town We dedicate this paper to the memory of the late Dr G. J. Broekhuysen, our former mentor and friend, who did more than any other person in laying the foundations for an eco-ethologica1 approach in scientific studies ofthe avifauna of the south-western Cape region ofSouth Mrica. ABSTRACT Cape sugarbirds, P,ome,ops cafe" preferred certain protea bushes as nest-sites. These bushes were characterized by relatively large leaves and dense foliage. Nests were usually placed in the central parts of bushes Nest-sites were shielded from the cold night sky, and were associated with relatively favourable air temperatures and protection from wind in a season of unfavourable weather. Data on microclimate of nest-sites, together with those on heat loss from an incubating sugarbird, were interpreted in relation to nest-site selection as adaptive behaviour promoting breeding success through conservation of energy. Sugarbirds nesting relatively high off the ground and in dense vegetation were considered to be decreasing the risk of exposure to predators. ) 0 1 0 2 d INTRODUCTION e t a d ( r Food availability, and shelter from predators and adverse weather are ultimate factors in habitat e h s selection in bird species (Baker 1938; Hilden 1965). Nest-site selection is not a random procedure, i l b and nest building will commence only when the summation of the heterogeneous stimuli of the u P micro-habitat exceeds the threshold for releasing nesting behaviour. -
The Functional Role of Birds As Pollinators in Southern Cape Fynbos
The functional role of birds as pollinators in southern Cape fynbos. Kellyn J. Whitehead A thesis presented in fulfilment of the academic requirements for the degree of Masters of Science in Ecological Sciences At the University of KwaZulu-Natal, Pietermaritzburg, South Africa January 2018 1 ABSTRACT Nectarivorous birds, particularly sunbirds, are important pollinators of plants in the Cape Flora of South Africa, being responsible for pollinating approximately 5% of plant species. However, interactions between plants and nectarivorous birds in the eastern part of the Cape Floristic Region have not received much attention. This study focussed on two putatively bird-pollinated plant species found within the Nature’s Valley area, namely Kniphofia uvaria and Chasmanthe aethiopica. The breeding systems were determined for each species and, due to their patchy population distribution, potential Allee effects on plant fecundity were also tested for. Flowering phenology in the area was also examined to test for associations between flowering of bird-pollinated plant species and the temporal presence of nectarivorous birds. Selective exclusion experiments showed that sunbirds were the main pollinators of K. uvaria and C. aethiopica – fruit set and the number of viable seeds were much higher for untreated (open control) individuals where birds could visit flowers freely, compared to caged individuals which only allowed for insect visitation. Very few seeds developed when plants of the two species were bagged to exclude all pollinators, indicating that the species are not capable of autonomous self-fertilization. Fruit and seed set were determined for patches of K. uvaria and C. aethiopica in order to test for potential Allee effects. -
Critical Resources and Habitats of the Endemic Fynbos Bird Community
Postdoctoral research proposal Climate Change Impacts on Fynbos Endemic Birds: Spatial and temporal patterns of abundance and dispersal of Fynbos avifauna Dr. Alan T. K. Lee Blue Hill Escape, P.O. Box 131, Uniondale, Western Cape, South Africa, 6460 044 752 1254 [email protected] Rationale Bird communities in the Fynbos biome face documented threats from alien vegetation encroachment, changes in burning regimes, and human modification of the landscape. The status of bird populations under current conditions has not been recently quantified, and while modelling assessments have determined that Fynbos bird species under vulnerable under various climate change scenarios no study has used real abundance data. There are six bird species recognised as globally restricted to the Fynbos. These are currently listed by IUCN conservation criteria as species of Least Concern, despite a lack of information on population size and little evaluation of population trends and range size changes. Recent reviews of their distribution, together with the impacts of climate change, suggest that their conservation criteria need to be re-examined. However, quantitative information on movements, densities and population sizes is lacking for most bird species that inhabit mountain Fynbos. This study aims to establish baseline density data for bird communities in the Mountain Fynbos habitat element; determine patterns of dispersal and abundance along aridity and altitudinal gradients to predict vulnerability of populations to future climate change; and determine how well these predictions could have been achieved using Southern African Bird Atlas Project data. Introduction Most of the Fynbos biome of the south-western and southern South Africa is included within the Cape Fynbos Endemic Bird Area (EBA), which extends from the Cederberg Mountains south and eastwards to Algoa Bay (BirdLife International 2010). -
Mite (Acari) Ecology Within Protea Communities in The
MITE (ACARI) ECOLOGY WITHIN PROTEA COMMUNITIES IN THE CAPE FLORISTIC REGION, SOUTH AFRICA NATALIE THERON-DE BRUIN Dissertation presented for the degree of Doctor of Philosophy in the Faculty of Agrisciences at Stellenbosch University Promoter: Doctor F. Roets, Co-promoter: Professor L.L. Dreyer March 2018 Stellenbosch University https://scholar.sun.ac.za DECLARATION By submitting this dissertation electronically, I declare that the entirety of the work contained therein is my own, original work, that I am the sole author hereof (save to the extent explicitly otherwise stated), that reproduction and publication therefore by the Stellenbosch University will not infringe any third party rights and that I have not previously in its entirety or in part submitted it for obtaining any qualification. ..................................... Natalie Theron-de Bruin March 2018 Copyright © 2018 Stellenbosch University All rights reserved i Stellenbosch University https://scholar.sun.ac.za GENERAL ABSTRACT Protea is a key component in the Fynbos Biome of the globally recognised Cape Floristic Region biodiversity hotspot, not only because of its own diversity, but also for its role in the maintenance of numerous other organisms such as birds, insects, fungi and mites. Protea is also internationally widely cultivated for its very showy inflorescences and, therefore, has great monetary value. Some of the organisms associated with these plants are destructive, leading to reduced horticultural and floricultural value. However, they are also involved in intricate associations with Protea species in natural ecosystems, which we still understand very poorly. Mites, for example, have an international reputation to negatively impact crops, but some taxa may be good indicators of sound management practices within cultivated systems. -
The Best of SOUTH AFRICA October 15-31 2018
TRIP REPORT: The Best of SOUTH AFRICA October 15-31 2018 The Best of SOUTH AFRICA Birding Safari October 15-31, 2018 Tour leaders: Josh Engel and David Nkosi Click here for the trip photo gallery Next trip: October 10-26, 2020 South Africa never fails to amaze. From the spectacular scenery and endemic birds of the Cape to the megafauna-filled wilderness of Kruger National Park, every single day brings something new, surprising, and awe-inspiring. This trip exceeded expectations—over 400 species of birds and an incredible 60 species of mammals, all seen while staying in interesting, varied, and excellent accommodations, eating delicious food, and thoroughly enjoying all aspects of traveling in South Africa. It’s hard to know where to start with bird and animal highlights. There are, of course, the most sought-after birds, like Protea Canary, Cape Rockjumper, Black Harrier, Rudd’s Lark, Black-eared Sparrowlark, Southern Black Korhaan, and Blue Korhaan. There were also the incredible bird experiences—the Shy Albatrosses surrounding our pelagic boat, the Cape Sugarbird singing from atop of king protea flower, the nest-building Knysna Turacos, the Water Thick-knees trying to chase a Water Monitor away from their nest. Mammals take a front seat in South Africa, too. We had incredible sightings of Leopard and Lion in Kruger, numerous White and a single Black Rhinoceros, along with many encounters with Elephant, Giraffes, and other iconic African animals. But we also saw many awesome small mammals, including Meerkat, Large- and Small- spotted Genet, White-tailed Mongoose, and a Cape Clawless Otter munching on a fish. -
The Cape Floristic Region
Ecosystem Profile THE CAPE FLORISTIC REGION SOUTH AFRICA Final version December 11, 2001 CONTENTS INTRODUCTION 3 THE ECOSYSTEM PROFILE 3 THE CORRIDOR APPROACH TO CONSERVATION 4 BACKGROUND 4 CONSERVATION PLANNING IN THE CAPE FLORISTIC REGION: THE CAPE ACTION PLAN FOR THE ENVIRONMENT (CAPE) 5 BIOLOGICAL IMPORTANCE OF THE CFR 7 LEVELS OF BIODIVERSITY AND ENDEMISM 7 LEVELS OF PROTECTION FOR BIODIVERSITY 9 STATUS OF PROTECTED AREAS IN THE CAPE FLORISTIC REGION 10 SYNOPSIS OF THREATS 11 LAND TRANSFORMATION 11 ECOSYSTEM DEGRADATION 12 INSTITUTIONAL CONSTRAINTS TO CONSERVATION ACTION 13 LACK OF PUBLIC INVOLVEMENT IN CONSERVATION 14 SYNOPSIS OF CURRENT INVESTMENTS 14 MULTILATERAL DONORS 16 NONGOVERNMENTAL ORGANIZATIONS 17 POTENTIAL INVESTMENT IN CAPE IMPLEMENTATION AND PROPOSED COMPLEMENTARITY WITH CEPF FUNDING 17 GOVERNMENT 18 NONGOVERNMENTAL ORGANIZATIONS 19 CEPF NICHE FOR INVESTMENT IN THE REGION 21 CEPF INVESTMENT STRATEGY AND PROGRAM FOCUS 22 SUPPORT CIVIL SOCIETY INVOLVEMENT IN THE ESTABLISHMENT OF PROTECTED AREAS AND MANAGEMENT PLANS IN CFR BIODIVERSITY CORRIDORS 24 PROMOTE INNOVATIVE PRIVATE SECTOR AND COMMUNITY INVOLVEMENT IN CONSERVATION IN LANDSCAPES SURROUNDING CFR BIODIVERSITY CORRIDORS 25 SUPPORT CIVIL SOCIETY EFFORTS TO CREATE AN INSTITUTIONAL ENVIRONMENT THAT ENABLES EFFECTIVE CONSERVATION ACTION 26 ESTABLISH A SMALL GRANTS FUND TO BUILD CAPACITY AMONG INSTITUTIONS AND INDIVIDUALS WORKING ON CONSERVATION IN THE CFR 27 SUSTAINABILITY 27 CONCLUSION 28 LIST OF ACRONYMS 29 2 INTRODUCTION The Critical Ecosystem Partnership Fund (CEPF) is designed to better safeguard the world's threatened biodiversity hotspots in developing countries. It is a joint initiative of Conservation International (CI), the Global Environment Facility (GEF), the Government of Japan, the MacArthur Foundation and the World Bank. -
Leucospermum R
Leucospermum R. Br. 1810 The type species is L. hypophyllocarpodendron, which was first described by Linneaus as a member of his large genus Leucadendron. Linneaus later moved this to Protea. Various authors prior to Robert Brown proposed names for Pincushions, these being Conocarpus Adanson 1763, Lepidocarpus Adanson 1763, and Leucadendrum Salisb. 1807. Robert Brown’s name is conserved. There are x sections of Pincushions, and we have followed Rourke’s (1972) treatment, with the exception of a new section discovered in 198* for the Hook Pincushions, and the removal of the section Xericola to the genus Vexatorella. Part 6 - 1 THE PROTEA ATLAS 1/25/2008 Leucospermum cuneiforme (Burm. f.) Rourke 1768, 1967 Wart-stemmed Pincushion Gewoneluisiesbos Other Common Names: Common Pincushion, Seedlings (1729 records): Absent in 97%: fewer Large-tufted Pincushion, Phyllanthus-leaf seedlings than prefire adults in 22 cases, and Leucadendrum, Stagshorn-leaf more in 8 cases. Seedlings found in Mar (3), Leucadendrum, Yellow Pincushion, Yellow- Apr (4), Jun (6), Jul (4), Aug, Sep, Oct (5), flame Pincushion, Boontjiesbos, Nov (3) and Dec (3). Geelspeldekussing, Klipboom, Fire Survival (292 records): 71% resprouted Kreupelbossie, Luisiesboom, Luisiesbos, from underground boles, 13% escaped fires Mielieput, Wildemielie. in fire-safe areas, 13% resprouted from aerial Other Scientific Names: attenuatum R.Br. trunks, 2% eliminated from the area by fires. 1810, cervinum (Salisb. ex Knight) 1809, Age to first flowering: First flowers recorded ellipticum (Thunb.) 1781, phyllanthifolium at 1 year, 50% estimated at 2-3 years, and (Salisb. ex Knight) 1809, septemdentatum reaching a peak of 90% at 4 years. Gand. & Schinz 1913, zeyheri Meisn. -
Proteaceae Floral Crops; Cultivar Development and Underexploited Uses
Proteaceae Floral Crops; Cultivar Development and Underexploited Uses Kenneth W. Leonhardt and Richard A. Criley The Proteaceae apparently originated on the southern supercontinent Gondwana long before it divided and began drifting apart during the Mesozoic era, accounting for the presence of the Proteaceae on all of the southern continents (Brits 1984a). The Protea family comprises about 1400 species in over 60 genera, of which over 800 species in 45 genera are from Australia. Africa claims about 400 species, including 330 species in 14 genera from the western Cape. About 90 species occur in Central and South America, 80 on islands east of New Guinea, and 45 in New Caledonia. Madagascar, New Guinea, New Zealand, and South- east Asia host small numbers of species (Rebelo 1995). Proteas are neither herbaceous nor annual, and they are always woody. Their structural habit is vari- able from groundcover forms with creeping stems, and those with underground stems, to vertical to spread- ing shrubs, to tree forms. The leaves are generally large, lignified, hard, and leathery. A mature leaf will generally snap rather than fold when bent. The leaf anatomy is specially adapted for water conservation and drought resistance. These characteristics and the high leaf carbon to nitrogen ratio render the leaves indi- gestible to most insect pests (Rebelo 1995), accounting for the relatively pest-free status of most commer- cial protea plantings. The distribution of the family is linked to the occurrence of soils that are extremely deficient in plant nutrients (Brits 1984a). An accommodating characteristic of the family is the presence of proteoid roots.