Hystrix Africaeaustralis – Cape Porcupine

Total Page:16

File Type:pdf, Size:1020Kb

Hystrix Africaeaustralis – Cape Porcupine Hystrix africaeaustralis – Cape Porcupine regions. Hunting for bushmeat and persecution for damage caused to fences and crops may result in local declines. Holistic management strategies, such as creating artificial passageways in game fences and establishing sustainable quill and meat trades, should be employed for this species, with positive effects for the wider socio-ecological community. Regional population effects: Extensive and well connected throughout all range states. Rescue effects are possible. Females do not conceive while living in their natal groups and dispersal is a prerequisite for successful reproduction (van Aarde 1987a; van Aarde & van Wyk 1991). However, it is unknown what distances they travel Christy Bragg when dispersing. Regional Red List status (2016) Least Concern Distribution National Red List status (2004) Least Concern Cape Porcupines have a wide distribution in sub-Saharan Reasons for change No change Africa, avoiding the tropical forests of the Congo basin, and the driest parts of the Namib Desert (Monadjem et al. Global Red List status (2016) Least Concern 2015). They occur from Kenya and southern Uganda in TOPS listing (NEMBA) (2007) None the north, through Tanzania, Rwanda, southeastern Democratic Republic of the Congo, extreme southwestern CITES listing None Congo, Angola, Zambia, Malawi and Mozambique, and Endemic No then south throughout southern Africa (although they are absent from much of central Botswana). Cape Porcupines are important Within the assessment region, they occur widely across all ecosystem engineers and thus play a valuable provinces, as well as Swaziland and Lesotho. For role in geophyte-rich ecosystems in sub-Saharan example, Power (2014) recorded them as common Africa. For example, in Nieuwoudtville, Northern throughout the North West Province, occurring in every Cape Province, their diggings contained vegetation type but showing some local preference for significantly more seedlings than adjacent areas riparian and rocky habitats. In the Drakensberg Midlands, and they displaced over 2.2 m3 of soil / ha / year, relative occupancy of ten terrestrial mammal species was thus helping to sustain landscape heterogeneity highest for Cape Porcupine (Ramesh & Downs 2015). (Bragg et al. 2005). They may be locally absent from some areas where there is high hunting pressure (Skinner & Chimimba 2005). Population Taxonomy It is a fairly common species across the assessment Hystrix africaeaustralis Peters 1852 region, with relatively high densities. For example, in the ANIMALIA - CHORDATA - MAMMALIA - RODENTIA - semi-arid landscapes around Nieuwoudtville, Northern HYSTRICIDAE - Hystrix - africaeaustralis Cape Province, burrow entrances were found to be a good predictor of the number of Porcupines it contained, Common names: Cape Porcupine, South African where occupied burrow density was estimated to be Porcupine (English), Ystervark (Afrikaans), Noko (Sepedi, 2.6 burrows / km2 and density on the study farm was Sesotho, Setswana), Ingungubane, Inungu (Swati, Zulu), estimated to be 8 individuals / km2 (Bragg et al. 2005). Nungu (Tsonga, Venda), This high density in a semi-arid area was proposed by Bragg et al. (2005) to be a result of the high food Taxonomic status: Species availability in the region (high geophyte density). However, Taxonomic notes: No subspecies have been recognised within more arid regions porcupine numbers can be as (Meester et al. 1986). low as 0.8 individuals / km2 such as in the Kalahari (Bragg, unpubl. data). Thus, we infer that there are over 10,000 mature individuals within the assessment region. Assessment Rationale However, hunting pressure and persecution (by farmers The species remains Least Concern in view of its wide and farm labourers because it is a considered an distribution within the assessment region, its occurrence agricultural pest, for bushmeat by rural communities, and in many habitats, including agricultural and urban for harvesting of the quills for use in the decor sector) may environments, and its relatively high densities in some account for local extinctions in some areas, and current Recommended citation: Bragg C, Child MF. 2016. A conservation assessment of Hystrix africaeaustralis. In Child MF, Roxburgh L, Do Linh San E, Raimondo D, Davies-Mostert HT, editors. The Red List of Mammals of South Africa, Swaziland and Lesotho. South African National Biodiversity Institute and Endangered Wildlife Trust, South Africa. The Red List of Mammals of South Africa, Lesotho and Swaziland Hystrix africaeaustralis | 1 Figure 1. Distribution records for Cape Porcupine (Hystrix africaeaustralis) within the assessment region Table 1. Countries of occurrence within southern Africa 1987b, 1987c). The inter-litter interval in captivity is approximately one year (van Aarde 1985b). Country Presence Origin Current population trend: Stable Botswana Extant Native Lesotho Extant Native Continuing decline in mature individuals: Locally, due to hunting pressure and persecution. Mozambique Extant Native Number of mature individuals in population: > 10,000 Namibia Extant Native Number of mature individuals in largest subpopulation: South Africa Extant Native Unknown Swaziland Extant Native Number of subpopulations: Unknown Zimbabwe Extant Native Severely fragmented: No. Can exist in human modified habitats. density estimates from throughout its range should be ascertained to determine population size more accurately. Habitats and Ecology Cape Porcupines live in extended family groups, They are found in most of the types of vegetation consisting of a breeding male, breeding female and encountered in southern Africa (including the coastal offspring of consecutive years (van Aarde 1987b). Female areas of the Namib Desert), from sea level to 2,000 m asl porcupine offspring do not conceive while in their natal (Skinner & Chimimba 2005). They are generally absent groups and thus dispersal is a prerequisite for from forest, and are only found here marginally. In reproduction (van Aarde 1987b). This has important Nylsvley Nature Reserve, Limpopo Province, they showed implications for the regulation of population size (van a preference for Burkea over Acacia savannah due to Aarde 1987a), because, if there are insufficient resources higher concentrations of food in the former (de Villiers et available in the environment, mature offspring cannot al. 1994; de Villiers & van Aarde 1994). In the Bokkeveld disperse from their natal group and thus cannot Plateau, in the Northern Cape, they showed seasonal reproduce (van Aarde 1987a, 1987b). In captivity, the changes in preference for habitats based on the habitat’s gestation period is c. 93 days, average litter size is 1–3, substrate, seasonal food availability and refuge capacity. and young are usually suckled for 100 days or more (van They can also exist in human-modified areas, such as Aarde 1985a, 1985b). Offspring attain sexual maturity croplands and suburban gardens. between 1–2 years of age, during which time annual survival is relatively high for a rodent (van Aarde 1987a, Porcupines feed predominantly on roots, geophytes and tubers, which are dug up from under the ground using Hystrix africaeaustralis | 2 The Red List of Mammals of South Africa, Lesotho and Swaziland Table 2. Use and trade summary for the Cape Porcupine (Hystrix africaeaustralis) Proportion of Category Applicable? Rationale Trend total harvest Subsistence use Yes Bushmeat and traditional medicine. Majority Unknown Commercial use Yes Traditional medicine and trophy hunting. Quill Minority Unknown décor industry. Harvest from wild population Yes All Majority Unknown Harvest from ranched population No - - - Harvest from captive population No - - - their strong incisors. Cape porcupines not only consume can dig up to 0.87 m3 of soil / hectare over a year, which is plants selectively (Bragg 2003; de Villiers & van Aarde equivalent to 5,859 tonnes / year and that their 1994) and sometimes en masse (Bragg 2003), but they disturbance can cover up to 510,391 m2 demonstrates the are also able to consume (without any apparent side- scale and intensity of their disturbance patterns (C. Bragg effects) geophyte species that are known to be toxic for unpubl. data). Cape Porcupine disturbance created livestock. They also feed on fallen fruits, and gnaw bones. distinct soil property changes in chemicals and moisture, Due to the combination of their diet and digging abilities, and probably also texture, and therefore creates a mosaic porcupines can become agricultural pests in farming of modified, unmodified and regenerating patches that areas (Monadjem et al. 2015). They do not appear to provide habitats of differing resource availability and scavenge (Shaw et al. 2015). They are nocturnal, territorial physical characteristics (C. Bragg unpubl. data). and solitary foragers, although they can occasionally be Additional disturbance impacts of Cape Porcupines take found foraging in groups of two to three animals. They are the form of the widespread distribution of their multi- monogamous and live in groups comprising either an entrance burrows (c. 60 on the 4,000 ha study area; Bragg adult pair, an adult pair and their offspring from et al. 2005). Cape Porcupines are also important patch consecutive litters, or an adult male and young of the year creators, such as shown by Bragg (2003) through their (Skinner & Chimimba 2005). They are long-lived and have maintenance of the Endangered Sparaxis pillansii a slow reproductive rate. geophytic species in the landscape of
Recommended publications
  • Hystrix Africaeaustralis)
    Reproduction in captive female Cape porcupines (Hystrix africaeaustralis) R. J. van Aarde Mammal Research Institute, University ofPretoria, Pretoria 0002, South Africa Summary. Captive females attained sexual maturity at an age of 9\p=n-\16months and con- ceived for the first time when 10\p=n-\25months old. Adult females were polyoestrous but did not cycle while lactating or when isolated from males. The length of the cycle varied from 17 to 42 days (mean \m=+-\s.d. 31\m=.\2\m=+-\6\m=.\5days; n = 43) and females experienced 3\p=n-\7 sterile cycles before conceiving. Pregnancy lasted for 93\p=n-\94days (93\m=.\5\m=+-\0\m=.\6days; N = 4) and litter intervals varied from 296 to 500 days (385 \m=+-\60\m=.\4;n = 10). Litter size varied from 1 to 3 (1\m=.\5\m=+-\0\m=.\66;n = 165) and the well-developed precocial young weighed 300\p=n-\400g (351 \m=+-\47\m=.\4g; n= 19) at birth. Captive females reproduced throughout the year with most litters (78\m=.\7%;n = 165) being produced between August and March. Introduction Cape porcupines (Hystrix africaeaustralis) inhabit tropical forests, woodlands, grassland savannas, semi-arid and arid environments throughout southern Africa. Despite this widespread distribution little attention has been given to these nocturnal, Old World hystricomorph rodents, which shelter and breed in subterranean burrows, rock crevices and caves. Some information on reproduction in female porcupines has been published on the crested porcupine (H. cristata) (Weir, 1967), the Himalayan porcupine (H. hodgsoni) (Gosling, 1980) and the Indian porcupine (H.
    [Show full text]
  • Celastraceae), a New Species from Southern Africa
    Phytotaxa 208 (3): 217–224 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.208.3.4 Putterlickia neglecta (Celastraceae), a new species from southern Africa MARIE JORDAAN1,3, RICHARD G.C. BOON2 & ABRAHAM E. VAN WYK1* 1H.G.W.J. Schweickerdt Herbarium, Department of Plant Science, University of Pretoria, Pretoria, 0002 South Africa. 2Environmental Planning and Climate Protection Department, eThekwini Municipality, Durban, 4000 South Africa. 3Previous address: South African National Biodiversity Institute, Private Bag X101, Pretoria, 0001 South Africa. *Author for correspondence. E-mail: [email protected] Abstract Putterlickia neglecta, a new species here described and illustrated, is known from South Africa (Mpumalanga and north- eastern KwaZulu-Natal), Swaziland and southern Mozambique. It is considered a near-endemic to the Maputaland Centre of Endemism. Plants grow as a shrub or small tree in savanna and thicket, or in the understory of inland, coastal and dune forests. Vegetatively it superficially resembles P. verrucosa, the species with which it has hitherto most often been confused. Both species have stems with prominently raised lenticels, but P. neglecta differs from P. verrucosa in having sessile to subsessile leaves with mostly entire, revolute leaf margins, flowers borne on pedicels 8–15 mm long, with petals up to 6 mm long and spreading or slightly recurved. Putterlickia verrucosa has leaves with distinct petioles, spinulose-denticulate mar- gins, much smaller flowers borne on pedicels up to 4 mm long, with petals up to 2 mm long and erect or slightly spreading.
    [Show full text]
  • Porcupine Wildlife Note
    24. Porcupine The porcupine is a blackish, quill-armored, slow-moving rodent with an appetite for tree bark and salt. It lives in forests and often can be seen hunched into what appears to be a black ball high in a tree. While it does not occur in all parts of Pennsylvania, the porcupine is one of Pennsylvania’s best-known and most easily identified wild animals. Its taxonomic name is Erethizon dorsatum. The word “porcupine” comes from two Latin words, porcus (“swine”) and spina (“thorn”), which also reflects the species’ colloquial name, quill pig. In the East, porcupines inhabit Canada and New England south into Pennsylvania; they range through the northern Midwest and the Pacific Northwest, south in the forested Rocky Mountains nearly to Mexico, and north to Alaska. They live at all elevations from sea level to timberline. Biology Adult porcupines are about 30 inches in length, including a 6- to 10-inch tail. They weigh 9 to 15 pounds, with bigger, older adults weighing up to 20 pounds. Males are larger than females. The porcupine is North America’s second largest rodent; only the beaver is bigger. Porcupines have four incisors—two above and two below that are bright orange, strong and adapted to gnawing. Short-legged and stout, a porcupine has a pronounced arch to its back. Its skull is heavily constructed; the small, longest), yellow or white tipped with black, and lined with rounded head has a blunt muzzle, ears almost hidden in a foam-like material composed of many tiny air cells. An fur, and dull black eyes.
    [Show full text]
  • Porcupine, Tree
    UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour Coendou prehensilis (Tree Porcupine or Brazilian Porcupine) Family: Erethizontidae (New World Porcupines) Order: Rodentia (Rodents) Class: Mammalia (Mammals) Fig. 1. Brazilian porcupine, Coendou prehensilis. [http://animaldiversity.ummz.umich.edu/site/resources/pablo_goncalves/Coendou2a.jpg/view.html, downloaded 22 November 2011] TRAITS. Coendou prehensilis, the Brazilian porcupine, is a mid-sized rodent with evolutionarily modified body hair. This modified hair exists as keratin-toughened, needle-like, semi-hollow quills or spines that grow to approximately 6.5cm in length. Like all New World porcupines, spines grow singly out of the skin and possess minute barbs at the end of the shaft. These spines cover the entire body, except for its fleshy nose, its belly and a large portion of its prehensile tail, and are usually light in colour (white to burnished yellow); there are also darker brown to black (soft/ unmodified) hairs interspersed along the body. It has small round eyes; and, a rounded yet flattened snout. The snout is covered with very short and very fine hairs and has several long whiskers. The porcupine has two long incisors and the front of its mouth that grows continuously during life and lacks canine teeth. At adult weight, this porcupine can range from 2kg to 5kg (Roberts et al., 1984). The average length of an adult Brazilian porcupine is approximately 90cm with its tail contributing about half of that length. Coendou also has modified padded feet with four long clawed toes. At birth, the infants are approximately 50cm head to tail, 0.415kg, are covered in reddish brown hair and have soft natal quills about 1.5cm in length that harden a few days after it is born.
    [Show full text]
  • Out of Europe: Investigating Hystrix Cristata (Rodentia: Hystricidae) Skull Morphometric Geographic Variability in Africa
    Biogeographia – The Journal of Integrative Biogeography 36 (2021): a001 https://doi.org/10.21426/B636051379 Out of Europe: Investigating Hystrix cristata (Rodentia: Hystricidae) skull morphometric geographic variability in Africa FRANCESCO M. ANGELICI1*, PAOLO COLANGELO2, SPARTACO GIPPOLITI3 1 FIZV, Via Marco Aurelio 2, I-00184 Rome (Italy) 2 Consiglio Nazionale delle Ricerche, Istituto di Ricerca sugli Ecosistemi Terrestri, CNR-IRET, Via Salaria km 29.300, I-00015 Montelibretti, Rome (Italy) 3 Società Italiana per la Storia della Fauna ‘Giuseppe Altobello’, Viale Liegi 48, I-00198 Rome (Italy) * corresponding author: [email protected] Keywords: Crested porcupine, geographic variability, Hystrix cristata senegalica, Hystrix cristata galeata, North-East Africa, taxonomy. SUMMARY The crested porcupine Hystrix cristata is one of the most well-known members of the Family Hystricidae, yet very little is known regarding its geographic variability in Africa. Two alternative hypotheses exist; pre-1940s classical taxonomy supported the existence of a distinct Eastern African species, Hystrix galeata, whereas recent molecular data seem to support only a North-South separation inside one single species, with the geographic-ecological barrier represented by the Sahara desert. Our morphometric data support the recognition of Hystrix cristata senegalica Cuvier, 1822 as the sub- Saharan representative of the species with a clear morphological difference between the North African and sub-Saharan crested porcupines, which seem re-conductible mostly to size difference. Within H. c. senegalica, our analysis seems to support a weak separation between the West African and the East African samples. Owing to considerable qualitative skull differences and overlooked molecular data, the taxonomic status of H. galeata remains uncertain as well as the status of porcupines of North-East Africa (Nubia).
    [Show full text]
  • Banded Mongoose
    Mungos mungo – Banded Mongoose Assessment Rationale The Banded Mongoose is listed as Least Concern as, although its distribution is restricted to the northeast of the assessment region, it is generally common in suitable habitat and is present in several protected areas. There are no major threats that could cause range-wide population decline. Accidental persecution through poisoning, controlled burning, and infectious disease may lead to local declines, whilst wildlife ranching might have a positive effect by conserving more suitable habitat and connecting subpopulations. Regional population effects: Dispersal across regional Chris & Mathilde Stuart borders is suspected as the range extends widely into Mozambique and is continuous into southeastern Regional Red List status (2016) Least Concern Botswana and southern Zimbabwe, and the species is not constrained by fences. National Red List status (2004) Least Concern Reasons for change No change Distribution Global Red List status (2016) Least Concern This species is distributed widely in sub-Saharan Africa TOPS listing (NEMBA) (2007) None from Senegal and Gambia to Ethiopia, Eritrea and Somalia, and south to about 31° in South Africa. It has CITES listing None been recorded to 1,600 m asl. in Ethiopia (Yalden et al. Endemic No 1996). Although fairly widespread in southern Africa, M. mungo appears to be rare in West Africa. Its relative In addition to living in groups numbering tens of scarcity in West Africa may be due to niche overlap with its individuals, Banded Mongooses are plural congener, the Gambian Mongoose (M. gambianus), breeders, females giving birth synchronously, and endemic to West Africa and reported to occupy similar provide cooperative care to the communal litter of habitat and have a similar diet (Cant & Gilchrist 2013; van pups (Cant & Gilchrist 2013).
    [Show full text]
  • South Africa 2017
    EXPEDITION REPORT Expedition dates: 1 – 27 October 2017 Report published: July 2020 Carnivores of the Cape Floral Kingdom: Surveying Cape leopards, caracals and other species in the fynbos mountains of South Africa EXPEDITION REPORT Carnivores of the Cape Floral Kingdom: Surveying Cape leopards, caracals and other species in the fynbos mountains of South Africa Expedition dates: 1 – 27 October 2017 Report published: July 2020 Authors: Alan T. K. Lee Blue Hill Nature Reserve | University of Cape Town | University of KwaZulu-Natal Gillian McGregor Rhodes University Alastair Potts Nelson Mandela University Matthias Hammer (editor) Biosphere Expeditions 1 © Biosphere Expeditions, a not-for-profit conservation organisation registered in Australia, England, France, Germany, Ireland, U , the International Union for the Conservation of Nature and the European Citizen Science Association. Abstract The fynbos biome of South Africa is a biodiversity hotspot renowned for its very high plant species richness, endemic birds and the presence of the Cape mountain leopard, a small race of African leopard Panthera pardus ssp pardus. Biodiversity monitoring across a range of faunal and floral taxa was conducted in mountain fynbos habitat. Studies were conducted for two weeks in October 2017, with the help of international citizen scientists recruited by Biosphere Expeditions and based at Blue Hill Nature Reserve (Western Cape). In this report we provide a status update on the leopards of Blue Hill Nature Reserve for the period 2016-2020 through photo records. Camera-trapping confirmed the presence of male leopard ‘Strider’, resident since 2015 until early 2019. It also captured a female, suspected of being accompanied by a nearly fully-grown cub.
    [Show full text]
  • Redunca Arundinum – Southern Reedbuck
    Redunca arundinum – Southern Reedbuck Assessment Rationale Although this species has declined across much of its former range within the assessment region, subpopulations have been reintroduced throughout much of its range, with sizeable numbers on private land. The mature population size is at least 3,884 on both formally protected areas and private lands (2010–2015 counts), which is an underestimate as not all private sector data are available. The largest subpopulation (420–840 mature individuals) occurs in iSimangaliso Wetland Park in KwaZulu-Natal (KZN). Based on a sample of 21 protected areas across the range of Southern Reedbuck, the overall Andre Botha population has increased by c. 68–80% over three generations (1997/2002–2015), which is driven primarily by the Free State protected areas, which have Regional Red List status (2016) Least Concern* experienced an average annual growth rate of 18% National Red List status (2004) Least Concern between 2006 and 2014. In the absence of the growth in the Free State, there has been a net 10–22% decline in the Reasons for change No change remaining 11 protected areas. This species experiences Global Red List status (2016) Least Concern local declines as it is vulnerable to poaching, illegal sport hunting and persecution, and demand for live animals for TOPS listing (NEMBA) (2007) Protected trade (possibly illegally taken from the wild). Empirical CITES listing None data indicate declines in some protected areas in KZN and North West provinces due to poaching, and anecdotal Endemic No reports suggest more severe declines outside protected *Watch-list Data areas due to poaching, sport hunting and habitat loss or degradation.
    [Show full text]
  • Digestive Physiology, Resting Metabolism and Methane Production of Captive Indian Crested Porcupine (Hystrix Indica)
    Journal of Animal and Feed Sciences, 28, 2019, 69–77 https://doi.org/10.22358/jafs/102741/2019 The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, Jabłonna Digestive physiology, resting metabolism and methane production of captive Indian crested porcupine (Hystrix indica) K.B. Hagen1, S. Hammer2, S. Frei1, S. Ortmann3, R. Głogowski4, M. Kreuzer5 and M. Clauss1,6 1 University of Zurich, Vetsuisse Faculty, Clinic for Zoo Animals, Exotic Pets and Wildlife, Winterthurerstr. 260, 15 8057 Zurich, Switzerland 2 Naturschutz-Tierpark Görlitz, Zittauerstrasse 43, D-02826 Görlitz, Germany 3 Leibniz Instiute for Zoo and Wildlife Research (IZW) Berlin, Alfred-Kowalke Str. 17, 10315 Berlin, Germany 4 Warsaw University of Life Sciences (WULS) – SGGW, Faculty of Animal Sciences, Department of Animal Breeding, Ciszewskiego 8, 02-786 Warsaw, Poland 5 ETH Zurich, Institute of Agricultural Sciences, Universitätsstr. 2, 8092 Zurich, Switzerland KEY WORDS: Hystricomorpha, Rodentia, ABSTRACT. Limited physiological measurements exist for the digestive mean retention time, digestibility, basal physiology of porcupines. We measured CH4 emission in three captive Indian metabolic rate, colonic separation mechanism crested porcupines (Hystrix indica; 16.1 ± 2.7 kg) fed a diet of pelleted lucerne, and measured feed intake, digestibility, and digesta mean retention time (MRT) of a solute and three particle markers (<2, 10 and 20 mm). Marker excretion patterns suggested secondary peaks indicative of caecotrophy, with MRTs of 26.4 h for the solute and 31.5, 26.8 and 26.2 h for the three particle markers, respectively. At a dry matter intake of 58 ±10 g/kg body mass0.75/day, Received: 29 November 2018 porcupines digested 49 and 35% organic matter and neutral detergent fibre, Revised: 9 January 2019 respectively, which is in the lower range of that expected for horses on a similar Accepted: 18 February 2019 diet.
    [Show full text]
  • Trophic Ecology of Rusty-Spotted Genet Genetta Maculata and Slender
    Trophic ecology of rusty-spotted genet Genetta maculata and slender mongoose Herpestes sanguineus in Telperion Nature Reserve, with a focus on dietary segregation as a possible mechanism of coexistence By Julia Zemouche 595534 A dissertation submitted in fulfilment of the requirements for the degree of MASTER OF SCIENCE (ZOOLOGY) in the School of Animal, Plant and Environmental Sciences at the University of the Witwatersrand 2018 Supervisor: Dr Zimkitha Madikiza Co-supervisors: Prof. Emmanuel Do Linh San (UFH) Dr W. Maartin Strauss (UNISA) Declaration I, Julia Zemouche (595534), hereby declare that this dissertation is my own unaided work. It is being submitted for the Degree of Master of Science at the University of the Witwatersrand, Johannesburg. It has not been submitted before for any degree or examination at any other university. Signature: ________________________________ 29/05/2018 i Acknowledgements First and foremost, I would like to acknowledge my supervisor, Dr Kim Madikiza, and co- supervisors, Prof. Emmanuel Do Linh San and Dr Maartin Strauss. You have provided endless support and guidance throughout this study, for which I am incredibly grateful. Your assistance in the field was always welcome and I learned a great deal from all of you. I would also like to thank the Oppenheimer family for allowing me to conduct my research at Telperion Nature Reserve. Special thanks go out to the various staff at Telperion who always made my visits pleasant and assisted me on many occasions. Ms. Rouxlyn Roux and Ms. Diana Moyo also deserve a special mention for assisting me with fieldwork and providing me with company.
    [Show full text]
  • Assessing the Effects of Climate Change on Distributions of Cape
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Stellenbosch University SUNScholar Repository Research Article Assessing the impacts of climate change on amphibians Page 1 of 7 Assessing the effects of climate change on AUTHORS: distributions of Cape Floristic Region amphibians Mohlamatsane M. Mokhatla1,2 Dennis Rödder3 G. John Measey2 Climatic changes have had profound impacts on species distributions throughout time. In response, species have shifted ranges, adapted genetically and behaviourally or become extinct. Using species distribution AFFILIATIONS: models, we examined how changes in suitable climatic space could affect the distributions of 37 endemic 1Department of Zoology, Nelson frog species in the Cape Floristic Region (CFR) – an area proposed to have evolved its megadiversity under Mandela Metropolitan University, a stable climate, which is expected to change substantially in future. Species distributions were projected Port Elizabeth, South Africa onto mean climate for a current period (1950 to 2000), hindcasted to palaeoclimate (Last Glacial Maximum; 2Centre for Invasion Biology, Department of Botany and LGM ≈ 21 kya and Holocene Glacial Minimum; HGM ≈ 6 kya) and forecasted for two emissions scenarios Zoology, Stellenbosch University, (A2a and B2a) for the year 2080. We then determined the changes in area sizes, direction (longitude Stellenbosch, South Africa and latitude), fragmentation index and biotic velocity, and assessed if these were affected by life-history 3Zoologisches traits and altitude. We found that the biotic velocity at which the CFR amphibian community is expected to Forschungsmuseum Alexander shift north (A2a ≈ 540.5 km/kya) and east (B2a ≈ 198 km/kya) far exceeds historical background rates Koenig, Bonn, Germany (≈1.05 km/kya, north and west ≈ 2.36 km/kya since the LGM).
    [Show full text]
  • Traditional Medicinal Animal Use by Xhosa and Sotho Communities in the Western Cape Province, South Africa Willem A
    Nieman et al. Journal of Ethnobiology and Ethnomedicine (2019) 15:34 https://doi.org/10.1186/s13002-019-0311-6 RESEARCH Open Access Traditional medicinal animal use by Xhosa and Sotho communities in the Western Cape Province, South Africa Willem A. Nieman1* , Alison J. Leslie1 and Anita Wilkinson2 Abstract Background: The use of animals and animal-derived materials in traditional medicine constitutes an important part of the belief systems of indigenous African cultures. It is believed to be rapidly expanding in South Africa, where traditional healers are estimated to outnumber western doctors by 2000:1 in some areas, with an overall clientele consisting of 60–80% of South African citizens. Despite concerns about the impact of the trade in traditional medicine on biodiversity, there has been only limited research on this topic in South Africa. Methods: Traditional Xhosa and Sotho healers operating from impoverished, rural communities in the Boland Region of the Western Cape Province were consulted to provide a comprehensive inventory of the number and frequency of animals used and sold. Species richness estimators, diversity indices, and a relative cultural importance (RCI) index were used to highlight species of concern and assess market dynamics. Results: A total of 26 broad use categories for 12 types of animal parts or products from 71 species or morphospecies were recorded. The most commonly sold items were skin pieces, oil or fat, and bones. Results showed that leopard, chacma baboon, Cape porcupine, monitor lizard species, puff adder, African rock python, and black-backed jackal were the species most used in the traditional medicinal trade.
    [Show full text]