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Red Hartebeest

Alcelaphus b. caama

2025 Red list status

Alcelaphus b. caama
Least Concern

2025 Red list status

Alcelaphus b. lichtensteinii
Not Applicable

Decline
Regional Population Trend

Unknown

Change compared to 2016

No Change

Overview
Red list assessment
Regional Distribution and Occurrence
Climate change
Population information
Population genetics
Habitats and ecology
Use and Trade
Threats
Conservation
Bibliography

Overview

Alcelaphus buselaphus caama – (Geoffroy Saint-Hilaire, 1803) 

ANIMALIA – CHORDATA – MAMMALIA – ARTIODACTYLA – BOVIDAE – Alcelaphus – buselaphus – caama 

Common Names: Red Hartebeest (English), Rooihartbees (Afrikaans), Ihlezu, Indluzele, Iqhama (Ndebele), Thetele (Sepedi), Kgama, Khama (Setswana), Kgama, Khama Lethodile, Tlohela (Sesotho), Umzansi (Swati), Nondo, Nondzo (Tsonga), Thendele (Venda), Ixhama (Xhosa),  Indluzela, Inkolongwane (Zulu)  

Taxonomic status: Subspecies 

Synonyms: No Synonyms 

Taxonomic Note:
Following Gosling and Capellini (2013), and in contrast to Grubb (2005), this species is considered to include both Red Hartebeest A. caama and Lichtenstein’s Hartebeest A. lichtensteinii. A total of eight subspecies are recognised, of which Red Hartebeest occurs in the assessment region and possibly (see discussion below) Lichtenstein’s Hartebeest. The eighth and nominate subspecies, the Bubal Hartebeest A. b. buselaphus, from North Africa is now Extinct (IUCN SSC Antelope Specialist Group 2016). 

Red List Status: Alcelaphus b. caama – LC – Least Concern 

Red List Status: Alcelaphus b. lichtensteinii – NA – Not Applicable 

Assessment Information

Assessors: Venter, J.A. 1 & da Silva, J.2

Reviewer: Shrader, AM.3

Contributor: Patel, T.4

Institutions: 1Nelson Mandela University, 2South African National Biodiversity Institute, 3University of Pretoria, 4Endangered Wildlife Trust 

Previous Assessor: Venter, J.A 

Previous Reviewer: Child, M.F. 

Previous Contributors: Gaylard, A. & Eksteen, J. 

Assessment Rationale 

Globally, Red Hartebeest is the most numerous subspecies (c. 130,000 animals) and is increasing. Although historically reduced from overhunting, it is now common within the assessment region, having been reintroduced into a number of formal and private protected areas across its range. The wildlife ranching industry also harbors a large number of animals on privately owned game farms and reserves. The population is widespread on formally protected areas and private land. Previously, the population increased in formally protected areas over three generations (1992–2015). Within the assessment region, there were at least 14,849 mature animals (assuming a 70% mature population structure) on formally protected areas, which increased to 38,511 mature animals by including private lands (2013/14 counts). However, based on recent data, many protected areas are showing a decline in numbers since 2016. As data were not robust enough to infer total estimates across the assessment region, the Least Concern listing remains. While there are no major threats, local threats, such as poaching, may cause declines outside protected areas. However, the effects of the wildlife industry on this species should be monitored, and hybridisation between Red Hartebeest, other hartebeest subspecies and other antelope species should be carefully regulated (for example, there should be no movement from the private sector into formally protected areas without genetic testing). This species is a key species for sustainable, wildlife-based rural economies and incentives should be put in place to conserve this species as wild and free-roaming herds on private land.  

Lichtenstein’s Hartebeest is Not Applicable within the assessment region, as there is much uncertainty over whether the subspecies was ever resident in both Kruger National Park (KNP) and northern KwaZulu-Natal Province (KZN) (for example, Pongola Nature Reserve). While they have been reintroduced into both KNP and private conservancies in the Lowveld, their numbers are currently very low within the assessment region (although their numbers were estimated to be 82,000 globally in 2008), probably comprising fewer than 50 individuals. Once further evidence has been produced to confirm or reject its historical residency in the assessment region, this subspecies should be reassessed. 

Regional population effects: Most of the population is fragmented through fencing. However, there is some local dispersal in the Kgalagadi Transfrontier Park between South Africa and Botswana depending on rainfall and local climatic variability. 

Reasons for Change 

Reason(s) for Change in Red List Category from the Previous Assessment: No change 

 Red List Index 

Red List Index: No change 

Recommended Citation: Venter JA & da Silva JM. 2025. A conservation assessment of Alcelaphus buselaphus caama. In Patel T, Smith C, Roxburgh L, da Silva JM & Raimondo D, editors. The Red List of Mammals of South Africa, Eswatini and Lesotho. South African National Biodiversity Institute and Endangered Wildlife Trust, South Africa.

Regional Distribution and occurrence

Geographic Range

Red Hartebeest occur throughout much of southern Africa (and marginally into Angola near the Namibian border) and, although much reduced by European colonists, their range is expanding again as they have been reintroduced into many protected areas and private game farms (and widely introduced outside their former range) (IUCN SSC Antelope Specialist Group 2016); for example, in Namibia (Skinner & Chimimba 2005). The bulk of the population in Botswana is in the southwest of the country in the Kalahari but they occur widely south of the Okavango (Skinner & Chimimba 2005). While Red Hartebeest historically occurred in the western lowlands of Lesotho, intense hunting and depredation have eradicated them from this area (Lynch 1994). They are widespread throughout South Africa extending eastwards from the Western Cape coastal areas along the coast and into the hinterland into the semiarid and savannah regions as well as Highveld grasslands, but the natural range does not extend into the Lowveld of Mpumalanga and Limpopo and northern KZN. It is widespread in protected areas throughout its range, and there is an increasing tendency for this species to be introduced onto private conservation areas. Currently, the subspecies now occurs in all provinces, which is echoed historically as numerous writers documented their occurrence throughout the Northern, Western and Eastern Cape provinces and in parts of the Free State, North West, Gauteng, KZN and Limpopo provinces (Handley 1961; Skinner & Chimimba 2005). Extra-limital introductions have, however, occurred in parts of the eastern Limpopo as well as Mpumalanga (where they are currently present in three provincial protected areas; J. Eksteen pers. comm. 2015) using animals from Namibia (Skinner & Chimimba 2005). They have also been introduced into Eswatini (IUCN SSC Antelope Specialist Group 2016). The Red Hartebeest as a subspecies (A. b. caama) naturally occurs in South Africa, Namibia, Botswana and Zimbabwe. 

The only part of their former range from which they were not entirely eliminated was the Northern Cape and presently herds move across the Botswana border onto farms in the province (Skinner & Chimimba 2005), which is corroborated by reports from the North West Province where the Moshita region harbours a naturally occurring, free-roaming subpopulation that probably originated from Botswana (Buijs 2010; Power 2014). 

Lichtenstein’s Hartebeest formerly occurred widely in the miombo woodlands of south-central Africa, but now occur mainly in wildlife areas in Tanzania, Mozambique and Zambia; they are extinct in Burundi (IUCN SSC Antelope Specialist Group 2016). Within the assessment region, they were probably present in low numbers in the Lowveld and northern KNP and KZN (du Plessis 1969; Milstein 1989; Skinner & Chimimba 2005), but were perhaps mistaken for Tsessebe (Damaliscus lunatus lunatus) in southern KNP (Penzhorn 1985). In 1985, 18 hartebeest were reintroduced from Malawi to KNP, a further 91 captive-bred individuals were released into northern KNP during 1990–1994, and 31 to the southern regions in 1994, but there are no further planned translocations into KNP (S. Ferreira pers. comm. 2014). In KZN, there were reports of hartebeest in Pongola as early as 1895 (Skinner & Chimimba 2005). Being ecologically unsuitable for Red Hartebeest, it is reasonable to assume the subspecies was Lichtenstein’s. They have also been reintroduced to some private reserves in the Lowveld. However, there is debate around whether this subspecies ever truly occurred in the assessment region or whether they were occasional visitors from their core range. For example, it was excluded from the previous assessment (Friedmann & Daly 2004). Supporting the exclusion, several older texts do not mention the subspecies as occurring in South Africa (Roberts 1951; Rautenbach 1982; Meester et al. 1986). More research is necessary to determine whether this subspecies was, or should be, native to the assessment region. 

Elevation / Depth / Depth Zones 

Elevation Lower Limit (in metres above sea level): 0 

Elevation Upper Limit (in metres above sea level): 4000 

Depth Lower Limit (in metres below sea level): (Not specified) 

Depth Upper Limit (in metres below sea level): (Not specified) 

Depth Zone: (Not specified) 

Map:

Figure 1: Distribution records for Red Hartebeest (Alcelaphus b. caama) within the assessment region (South Africa, Eswatini and Lesotho). Note that distribution data is obtained from multiple sources and records have not all been individually verified.

Biogeographic Realms 

Biogeographic Realm: Afrotropical, Palearctic 

Occurrence 

Countries of Occurrence 

Country  Presence  Origin  Formerly Bred  Seasonality 
Algeria  Extinct Post-1500  Native     
Angola  Extant  Native     
Benin  Extant  Native     
Botswana  Extant  Native     
Burkina Faso  Extant  Native     
Cameroon  Extant  Native     
Central African Republic  Extant  Native     
Chad  Extant  Native     
Congo, The Democratic Republic of the  Extant  Native     
Côte d’Ivoire  Extant  Native     
Egypt  Extinct Post-1500  Native     
Eritrea  Extant  Native     
Eswatini  Extant  Introduced     
Ethiopia  Extant  Native     
Gambia  Extant  Native     
Ghana  Extant  Native     
Guinea  Extant  Native     
Guinea-Bissau  Extant  Native     
Kenya  Extant  Native     
Lesotho  Extinct Post-1500  Native     
Libya  Extinct Post-1500  Native     
Mali  Extant  Native     
Morocco  Extinct Post-1500  Native     
Namibia  Extant  Native     
Niger  Extant  Native     
Nigeria  Extant  Native     
Senegal  Extant  Native     
Somalia  Extinct Post-1500  Native     
South Africa  Extant  Native     
Sudan  Extant  Native     
Tanzania, United Republic of  Extant  Native     
Togo  Extant  Native     
Tunisia  Extinct Post-1500  Native     
Uganda  Extant  Native     

Large Marine Ecosystems (LME) Occurrence 

Large Marine Ecosystems: (Not specified) 

FAO Area Occurrence 

FAO Marine Areas: (Not specified) 

Climate change

Climate change may make the western parts of South Africa drier in the coming years, and Red Hartebeest are particularly susceptible to drought. For example, many carcasses were found on Molopo Nature Reserve in North West Province following drought conditions (Nel 2015). Further research needs to be conducted on the possible effect of climate change on the vulnerability of this species. 

Population information

Globally, East (1999) estimated the total population of all hartebeest at about 362,000 animals (including Lichtenstein’s), the majority of which are Red Hartebeest, estimated to number about 130,000 animals on both private and formally protected land. The population is widespread and thriving within the assessment region. On protected areas alone, there were a minimum observed number of 21,213 animals in 70 reserves (2013/14 counts), with the largest subpopulations occurring in the South African side of Kgalagadi Transfrontier Park (1,925 animals in the wet season of 2012; Ellis & Herbst 2013), Golden Gate Highlands National Park (1,646 animals in 2016; Bissett et al. 2016b), and Karoo National Park (1,650 animals in 2015; Gaylard et al. 2016). Interestingly, all of these protected areas have shown a decline in numbers since 2016 (SANParks data). 

Some large private wildlife reserves (such as Tswalu Kalahari Reserve and Khamab Kalahari Reserve) also contained subpopulations in excess of 1,000 animals. Including animals on private lands increased the population estimate to a minimum number of 55,016 animals (2013/14 counts) on 726 properties. This yields a total estimated mature population size (assuming 70% mature population structure) of 14,849–38,511 animals in 2013/14. However, the most recent count for Khamab Kalahari Reserve showed 485 individuals, indicating a decline in numbers in both protected and private reserves. 

Generation length has been calculated as 7.8 years (Pacifici et al. 2013), which yields a three-generation window of 23.5 years (1992–2015). During the 2016 assessment, trends on protected areas indicated a positive growth rate over three generations (Peinke & Gibisela 2014; for example, Nel 2015; Bissett et al. 2016a, 2016b; Ferreira et al. 2016; Gaylard et al. 2016). This trend has changed, however, and several state protected areas are showing significant declines since 2016. In North-West Province for example, the total population in provincial protected areas has declined by 7% with at least two protected areas losing more than 80% of their Red Hartebeest populations (NorthWest Parks and Tourism Board, 2023). This subspecies generally thrives in protected areas. Following the incorporation of QwaQwa National Park into Golden Gate Highlands National Park in 2008 (increasing the size of the protected area to 327 km2), Red Hartebeest increased from 346 in 2002 to 1,646 in 2016 (Bissett et al. 2016b). However, the population dropped to 762 in 2018, and further declined to 574 in 2020 (SANParks counts).  

Population Information 

Current population trend: Previously increasing, currently unknown – many protected and private areas are showing a decline in numbers since 2016. 

Continuing decline in mature individuals? Unknown 

Severely fragmented: Yes. Most subpopulations exist within fenced areas, relying on translocation for gene flow. However, some farms are fenced with cattle fencing which may allow herds to move between farms. 

Extreme fluctuations in the number of subpopulations: (Not specified) 

Continuing decline in number of subpopulations: (Not specified) 

All individuals in one subpopulation: (Not specified) 

Number of subpopulations: 70

Quantitative Analysis 

Probability of extinction in the wild within 3 generations or 10 years, whichever is longer, maximum 100 years: (Not specified) 

Probability of extinction in the wild within 5 generations or 20 years, whichever is longer, maximum 100 years: (Not specified) 

Probability of extinction in the wild within 100 years: (Not specified) 

Population genetics

The eight recognised subspecies of A. buselaphus were described based on variation in horn shape and size, coat colour and body size (Sidney, 1965); however, these designations are not validated using molecular evidence. Instead, the eight subspecies have been shown to cluster within two evolutionarily significant units (ESUs) – northern and southern (Arctander et al. 1999; Flagstad et al. 2001; Ouma et al. 2011; Russo, unpublished data). The composition of each ESU is as follows: Northern – A. b. buselaphus, A. b. major, A. b. tora, A. b. lelwel, A. b. swaynei, A. b. cokii – and Southern – A. b. caama; A. b. lichtensteinii.  Within the assessment region, a single ESU (Southern) is present.    

Within this southern ESU, two Management Units (MUs) have been identified. The South-Western MU comprises A. b. lichtensteinii individuals and is believed to span South Africa (Kruger National Park only), Zimbabwe, Mozambique, Zambia, southern Democratic Republic of the Congo, Malawi, southern Tanzania.  

Habitats and ecology

Red Hartebeest prefer open habitat and mainly occur in grasslands of various types (Skinner & Chimimba 2005). More tolerant of woodland areas and high grass than other alcelaphines, Hartebeest prefer the edge to the middle of open plains (Gosling & Capellini 2013). They thus appear to be an edge or ecotone species (Booth 1985), generally avoiding more closed woodland, and sometimes they occupy high-lying areas that are avoided by most other larger grazers (J. Eksteen unpubl. data). They occur on floodplain grassland, vleis, semi-desert savannah and open woodland (Skinner & Chimimba 2005). 

Red Hartebeest are considered to be predominantly selective grazers that will make use of browse under limited resource conditions (Murray & Brown 1993). They feed selectively in medium-height grassland; they are less water-dependent than other alcelaphines, but nonetheless dependent on the availability of surface drinking water (IUCN SSC Antelope Specialist Group 2016). In areas with much moribund vegetation, the Red Hartebeest faces particular constraints because nearly all vegetation biomass is of low quality, which reduces food intake rates (Drescher et al. 2006a, 2006b; van Langevelde et al. 2008). Under these conditions grassland fire plays an important role in providing suitable grazing conditions for this species (Venter et al. 2014). Additionally, the hartebeest skull morphology is specially adapted to be very selective at times when good forage is scarce (Schuette et al. 1998). They are gregarious, occurring in herds of up to 20 but can occur in much larger herds (Skinner & Chimimba 2005). Among the various hartebeest subspecies, a positive correlation between mean body size and rainfall suggests that habitat productivity may drive morphological evolution between ecotypes (Capellini & Gosling 2007). 

Ecosystem and cultural services: In Bushman folklore the hartebeest and the Eland (Taurotragus oryx) have magical power. A woman who has a young child does not eat hartebeest meat. The head and hide of a Hartebeest were sometimes worn over men’s shoulders when hunting large animals like African Elephants (Loxodonta Africana) or Eland. Whilst advancing towards their quarry through the grass, they would carefully mimic the actions of the hartebeest. 

IUCN Habitats Classification Scheme 

Habitat  Season  Suitability  Major Importance? 
1.5. Forest -> Forest – Subtropical/Tropical Dry    Marginal   
1.6. Forest -> Forest – Subtropical/Tropical Moist Lowland    Suitable   
1.9. Forest -> Forest – Subtropical/Tropical Moist Montane    Suitable   
2.1. Savanna -> Savanna – Dry    Suitable   
2.2. Savanna -> Savanna – Moist    Suitable   
3.4. Shrubland -> Shrubland – Temperate    Suitable   
3.5. Shrubland -> Shrubland – Subtropical/Tropical Dry    Suitable   
4.4. Grassland -> Grassland – Temperate    Suitable   
4.5. Grassland -> Grassland – Subtropical/Tropical Dry    Suitable   

Life History 

Generation Length: 7.8 years (Pacifici et al. 2013) 

Age at maturity: Female or unspecified: (Not specified) 

Age at Maturity: Male: (Not specified) 

Size at Maturity (in cms): Female: (Not specified) 

Size at Maturity (in cms): Male: (Not specified) 

Longevity: (Not specified) 

Average Reproductive Age: (Not specified) 

Maximum Size (in cms): (Not specified) 

Size at Birth (in cms): (Not specified) 

Gestation Time: 8 months 

Reproductive Periodicity: (Not specified) 

Average Annual Fecundity or Litter Size: One calf 

Natural Mortality: (Not specified) 

Does the species lay eggs? No 

Does the species give birth to live young: Yes 

Does the species exhibit parthenogenesis: No 

Does the species have a free-living larval stage? No 

Does the species require water for breeding? No 

Movement Patterns 

Movement Patterns: (Not specified) 

Congregatory: (Not specified) 

Systems 

System: Terrestrial 

General Use and Trade Information

This species is used in live animal trading at game auctions, and has a subsistence value as bushmeat or for recreational biltong hunters as they have high-quality meat (Gosling & Capellini 2013). The hartebeest also has national and international value as a species suitable for trophy hunting. This appears to have had no negative effect on the population as its value as a trophy animal ensures an increase in numbers due to reintroductions to game farms. Hunting quotas also benefit communal areas in some regions (Buijs 2010). There is also some captive breeding of hartebeest (IUCN SSC Antelope Specialist Group 2016), but this is limited. 

Wildlife ranching and the private sector have generally had a positive effect on this species as it has been widely reintroduced onto private properties within its natural distribution range. Most populations on wildlife ranches are free-roaming. Ranches are generally a few hundred hectares in the central and northern parts of the country to several thousand hectares in the more arid areas of the Northern Cape. Some of the very large privately owned reserves in this area have populations in excess of 1,000 individuals and therefore contribute significantly to the regional population. Due to its value (medium priced) and popularity as a trophy hunting animal, it is a popular species to have amongst game farm owners. Captive breeding of this species is not common and currently hybrids or colour variants do not feature in the live sale market. 

Subsistence:  Rationale:  Local Commercial:  Further detail including information on economic value if available: 
Yes  Bushmeat and biltong hunting.  Yes  Trophy hunting and live sales. 

National Commercial Value: Yes 

International Commercial Value: No 

End Use  Subsistence 
1. Food – human  true 
15. Sport hunting/specimen collecting  true 

Is there harvest from captive/cultivated sources of this species? Yes 

Harvest Trend Comments: Most commercial use occurs in wildlife ranches and game farms. Limited captive breeding.  

Threats

Globally, as the bushmeat trade escalates out of control (Lindsey et al. 2013), many hartebeest populations are being hunted to extinction (IUCN SSC Antelope Specialist Group 2016). The Red Hartebeest population within the assessment region occur in a number of protected and private reserves, however, many are experiencing declines. Poaching is a localised threat; for example, on Borakalalo National Park, North West Province (Nel 2015). 

Ongoing threats to this subspecies are habitat loss and habitat degradation. Ongoing habitat conversion from agriculture, livestock farming and commercial development make habitat less available or less suitable for future reintroductions into such areas. The distributions of most hartebeest subspecies are likely to become increasingly fragmented until they are confined to those areas where there is effective control of poaching and encroachment by livestock and settlement (IUCN SSC Antelope Specialist Group 2016). However, the Songimvelo subpopulation showed an increasing trend despite an increase in competition from livestock; in the same period that the Sable (Hippotragus niger niger) subpopulation declined (J. Eksteen unpubl. data). 

This subspecies is suspected to be hybridised with other hartebeest subspecies and with Blesbok (Damaliscus pygargus phillipsi), Bontebok (D. p. pygargus) and Tsessebe (Damaliscus lunatus lunatus) on private lands. This may make certain subpopulations ineligible for Red List assessment and may threaten the genetic integrity of the subspecies overall. This practice, while currently not common, should be disincentivised. 

Conservation

Red Hartebeest are well protected across their range within the assessment region. No direct interventions are currently necessary for this subspecies. However, continued protected area expansion to connect fragmented subpopulations and restrictions on the introduction of extra-limital subspecies/species, especially on private lands, will increase the long-term resilience of the population.

Recommendations for land managers and practitioners 

Drop internal fences to form conservancies so as to encourage greater movement within the landscape and thus less habitat degradation at the local scale.  

 Research priorities

Research is currently being conducted by Eastern Cape Parks and Tourism Agency on movement and feeding ecology of the subpopulation in Mkambati Nature Reserve. UNISA’s College of Agriculture and Environmental Sciences is conducting some research on the physiology of the subspecies in the Northern Cape.

Research priorities include: 

  • Determine the current estimate of Red Hartebeest within the assessment region. 
  • Quantifying the severity of bushmeat poaching. 
  • Quantifying vulnerability to climate change. 
  • Genetic work on wild subpopulations (Kalahari, Namibia and other regions) to establish if any genetically distinct subpopulations exist. 

Encouraged citizen actions: 

  • Landowners should create conservancies for this species and engage local stakeholders to create sustainable, wildlife-based rural economies. 
  • Report sightings of free-roaming herds outside private lands or protected areas on virtual museum platforms (for example, iNaturalist and MammalMAP). 

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