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South African Journal of Science

On-line version ISSN 1996-7489
Print version ISSN 0038-2353

S. Afr. j. sci. vol.115 n.3-4 Pretoria Mar./Apr. 2019

http://dx.doi.org/10.17159/sajs.2019/4805 

REVIEW ARTICLE

 

The decline of the Knysna elephants: Pattern and hypotheses

 

 

Lizette MoolmanI; Sam M. FerreiraII; Angela GaylardI; Dave ZimmermanIII; Graham I.H. KerleyIV

IScientific Services, South African National Parks, Knysna, South Africa
IIScientific Services, South African National Parks, Skukuza, South Africa
IIIVeterinary Wildlife Services, South African National Parks, Port Elizabeth, South Africa
IVCentre for African Conservation Ecology, Department of Zoology, Nelson Mandela University, Port Elizabeth, South Africa

Correspondence

 

 


ABSTRACT

Understanding and identifying drivers of local population declines are important in mitigating future risks and optimising conservation efforts. The Knysna elephants have, after being afforded protection since the early 1900s, declined to near extinction today. We propose three hypotheses as to why the Knysna elephant population declined. The refugee hypothesis suggests that anthropogenic activities forced the elephants to take refuge in the forest and that the low-quality food acted as the primary driver of decline. The illegal killing hypothesis suggests that the elephants adapted to the forest and its immediate fynbos habitat, with the decline being a consequence of illegal kills. The stochastic founder population hypothesis postulates that the population size and structure left it vulnerable to demographic stochasticity. We critically reviewed available evidence for these hypotheses and found that, although the historical elephant range decline most likely resulted through the refugee hypothesis, the weak demographic and life-history information limits elimination of either of the other hypotheses. We touch on the implications for decision-makers and draw attention to information requirements.
Significance:
We highlight the knowledge and management challenges which exist for small, threatened populations of which long-term demographic data are sparse.
We provide the first unbiased evaluation of multiple drivers that may have caused the decline of the Knysna elephants

Keywords: refugee populations; illegal killing; stochasticity


 

 

Introduction

African elephants, Loxodonta africana, are declining across the continent, largely because they are poached for their ivory.1 In contrast to continental trends, elephant populations in South Africa have increased in recent years.2 The Knysna elephants, however, are an anomaly. They are the most southern group of elephants in Africa, the only remaining free-ranging elephants in South Africa and represent one of four relict populations in the country.3 This small population failed to flourish after official protection was afforded in 1908, and its chances for persistence are of concern. Here we review the history of this population and develop and explore hypotheses that may explain why this small population failed to recover after protection.

Based on an estimated 3000 elephants that roamed the Cape Floristic Region in pre-colonial times4, it is likely that about 1000 elephants occupied the Outeniqua-Tsitsikamma area5. Between 1856 and 1886, Knysna experienced a marked influx of people and a boom in development which increased human-elephant conflict, often at a cost to the elephants.6 During the late 1800s, an estimated 400 to 500 elephants lived in the area7, but by 1900, only 30-50 individuals were left3.

During the early 1900s, attitudes shifted from regarding the elephants as a nuisance towards favouring them as local assets.6 Since then, the question of how many elephants are left in the Knysna forest has prevailed among conservationists, scientists and the public. Numerous survey attempts followed, often accompanied by suggestions on how to recover the population.7-12

Management of this population is challenging if the cause of the decline is not clear.13 A key question is thus, why has the population declined even after official protection since 1908?9,11,14-17 We propose three hypotheses for the decline. The refugee species hypothesis suggests that human disturbance and encroachment displaced the local elephants from other more optimal habitats into poor-quality habitats of the forests and its surrounding fynbos.18 The decline then resulted from a limitation of good-quality food.17 The illegal killing hypothesis suggests that the decline resulted from illegal killing.11,19 The stochastic founder population hypothesis suggests that the founder population's small size and its structure lead to demographic stochasticity13 that significantly constrained recovery.

Here we review evidence for and perceptions around these three hypotheses. In addition, we discuss information gaps and the management implications of our findings for decision-making on the future of the Knysna elephants.

 

The refugee hypothesis

Refugee populations are separated from optimal habitats and are confined to suboptimal habitats. This in turn leads to decreased fitness and smaller populations.18 The Knysna elephants are candidates for refugee status based on their decline in range, fitness and density.18

Researchers have suggested that human settlement and agricultural development taking place in the more open areas confined the southern Cape elephant population's historical range to the southern Cape forests.17,20,21 As early as 1755, travellers in the southern Cape noted the ongoing shooting of the elephants, which subsequently resulted in the elephants seeking refuge in the forests in the Tsitsikamma area.22 This record implies that these elephants chose the forests as they provided safety from human disturbances, rather than for nutritional and other life-history needs.

The effects of human disturbances on elephant ranging, movement and distribution patterns and behaviour elsewhere illustrate how elephants avoid such disturbances23-26, which lead to declines in elephant ranges. Such populations remain fragmented within their original distribution range, often in suboptimal habitat that may lead to decreases in fitness.18

Here we review available evidence relevant to the refugee concept for the Knysna elephant population. We focus on the historical range decline followed by habitat and resource quality as limits of persistence for a refugee elephant population. We also use a once-off reintroduction of elephants as a case study to evaluate the refugee hypothesis.

Safety - historical range decline

The refugee concept suggests that the range of the Knysna elephant population declined from them living in historically open areas to being confined to the forest and its immediate surrounding fynbos habitat. Genetic evidence illustrates that the Knysna elephants once belonged to a single South African population27, which ranged widely across South Africa from the Cape Peninsula to Limpopo3,20. This large historical population occurred in eight different biomes - Fynbos, Succulent Karoo, Desert, Nama-Karoo, Grassland, Savanna, Albany Thicket and Forest.28 Today, the Knysna elephants have access to only two habitat types - the afro-temperate forest and immediate surrounding fynbos. Their modern-day range, about 185 km2 in size, spans the fragmented afro-temperate forest which occurs mostly on the footslopes of the Outeniqua mountain range, interspersed with fynbos and commercial pine plantations.

Historically, elephants occupied open areas of varied habitat types outside of the southern Cape afro-temperate forests. Elephants were observed between Mossel Bay and George in 1497 by Vasco da Gama, in 1601 by Paulus van Caerden29 and between 1773 and 1776 by other travellers30. Local farmers and residents regularly reported elephant sightings east of George in the late 1800s6 with records at Wittedrift (north of Plettenberg Bay) dated 1782 and 181629. Further away, in the Little Karoo, local newspapers31 reported a 'troop' of elephants barring the road to the Uitenhage Ostrich Farming Company in 1883. Further east, in the Langkloof, Sparrman recorded elephants close to Humansdorp in 1775, as did Rev C.l. la Trobe in 1816.29

Increases in human settlement and population growth, the growing ivory trade, and crop protection exterminated most of South Africa's elephant population between 1652 and 1870.3 Demand for ivory as well as habitat transformation were the main driving forces for the southern Cape elephants' demise in the 19th century.32 The expulsion of elephants from open areas outside the southern Cape forests6,15,17,33 started taking place in the late 1700s29. The pressures and dangers that existed for the elephants on the perimeters and in neighbouring areas to the Outeniqua (Knysna) and Tsitsikamma forests were ongoing during the 18th century. Anders Sparrman wrote in 1775 of the continuous shooting of elephants in the George and Knysna areas29 while Le Vaillant recorded elephant pitfalls at Kaaimansgat, east of George, in 178230. This small population survived most likely because hunters had difficulty in finding them in the forest terrain.29 These historical accounts suggest that elephants primarily moved into the forest areas to avoid human disturbances.

Food quality

A second element of the refugee hypothesis is that confinement of Knysna elephants to suboptimal habitats affected their fitness and that ultimately led to their decline. The range of modern-day Knysna elephants covers afro-temperate forest, fynbos and commercial pine plantations growing on nutrient-poor soils derived from sandstone.34 Several studies have attempted to evaluate the link between low nutrients of forest plants and the Knysna elephant decline15,17,21,35, but with no conclusive support or rejection of the suboptimal habitat concept.

Key studies focused on Knysna elephant faecal and browse mineral contents15,21,35 and faecal N/C ratios17. These studies hypothesised nutrient and mineral deficiencies as the primary drivers of the decline in elephant numbers. However, these assessments were lacking knowledge of what constitutes diet deficiencies that affect fitness for wildlife as most of this information is available mainly for domestic and laboratory animals.36 Koen and colleagues15,21,35 used nutrient limits set for domestic livestock for the Knysna elephant diet assessment, but acknowledged that livestock nutrient limits are unreliable standards for assessing elephant diet deficiencies.

Because of their simple digestive systems, which have relatively low digestive efficiency as a result of fast passage, and their low metabolic rate per unit of body mass, elephants can tolerate lower quality forage than smaller herbivores can, but require a higher abundance of plants.37 Olff38 illustrated that, on a global scale, the occurrence of elephant and Cape buffalo was independent of plant-available nutrients and dependent on plant-available moisture. In east and southern Africa, megaherbivore abundance increased with rainfall, but was independent of soil nutrient status and it was suggested that megaherbivores are therefore limited by food quantity and not quality.39

A second approach to quantify potential Knysna elephant diet deficiencies and consequences for fitness focused on comparing browse and faecal nutrient and mineral contents with those of fit elephant populations such as those of the Addo Elephant National Park (AENP) and Kruger National Park15,17,21, both of which have a higher soil nutrient status. Alternatively, more insightful comparisons would be between the Knysna population and healthy, growing populations occurring in other areas of low habitat quality or soil nutrient status e.g. in the Kalahari-sand region of Hwange National Park in Zimbabwe40 or Tembe Elephant Park in KwaZulu-Natal, South Africa41. Sodium concentrations are extremely low throughout elephant ranges40,42 which suggests that elephants may require much lower concentrations of sodium to maintain condition and survival than commonly perceived43.

Finally, a key mechanism associated with the low N/C ratio in the Knysna elephant faeces, results from the lack of C4 grasses in the Knysna elephants' forest range.17 In areas where African elephant populations have access to woodlands, forests and grassland habitats, they prefer grass species during the rainy season and browse species during the dry season.44,45 Isotope records in historical and prehistoric elephant bones originating from areas in the Western Cape, however, illustrate that these elephants utilised much less C4 grass than elephants in the Kruger National Park, suggesting that C4 grasses cannot be considered a limiting factor in elephant distribution.46 This finding implies that the lack of C4 grasses in the Knysna elephant range may not be an indicator of suboptimal habitat.

The failure of an introduction of some elephants sourced from Kruger National Park to the Knysna forest was linked to the low quality of the local food17, which would support the suboptimal habitat concept and refugee hypothesis. This link was based on a prediction that the introduced elephants would bond and remain with the native elephants in the forest. The Kruger elephants, however, rejected the forest habitat and spent most of their time on neighbouring farmland.16,17 It was suggested that they did so in search of more nutritious food.17 However, more recent knowledge on elephant behaviour and translocations suggests otherwise (Box 1).

Calf mortality may reflect the outcomes of nutritional stress. If the habitat quality in the Knysna forest and fynbos is inadequate as suggested15,17,21,35, it may have contributed to the high calf mortality observed. Female elephants under nutritional stress have been shown to have calves which have lower survivorship.51 A high calf mortality was reported for the Knysna population in the 1900s.7-10,52,53 Phillips7 noted for the Knysna population that several calves died between 1922 and 1925 and dead calves were found in 1937, 19429 and in 196816. Calf mortality of the Knysna population was estimated to be between 60% and 80%, compared with 7.5% for the AENP population.53

Historical records support the refugee hypothesis by illustrating how people forced the southern Cape's elephants out of open areas and into the forest and its surrounding fynbos. A link between the Knysna elephant decline and habitat quality could, however, not be made with the information available.

 

The illegal killing hypothesis

The illegal killing hypothesis suggests that elephants were adapted to the forest and fynbos habitats, and their decline resulted from illegal killing.11,19 Predictions of forest adaptation focused on attempts to describe the Knysna elephants as a different sub-species.11,54 Lydekker54 assigned the Knysna elephant as Elephas africanus toxotis, based on comparisons of ear-shapes of specimens from Knysna and AENP, but later discovered that the museum specimen labelled as a Knysna elephant, was in fact a specimen from the Addo area14. Carter11 speculated that although these elephants are L. africana and not a sub-species, their 'habits appeared to have become modified for existence in the forest'. This perception of forest adaptation remains, and media, blogging sites and local tourism and property agencies' brochures refer to Knysna's forest elephants. There is, however, no published evidence of genetic, behavioural or morphological adaptations of the Knysna elephants to forest habitats.

Official protection was realised when the Knysna elephants were declared Royal Game in 1908.17 In 1920, authorities issued Major P.J. Pretorius with a permit to shoot one elephant for scientific purposes - a hunt which ultimately caused the death of five elephants.16 In 1971, an old bull known as Aftand was shot by forestry officials because of his crop-raiding behaviour on smallholdings.16 Apart from this shooting, there were no elephant shootings officially reported after 1908.17

Although the elephants roamed mostly on forestry land, forestry officials had no authority to protect the elephants when they moved off forestry land, even after they were declared Royal Game.53 Speculations claimed that the Forestry Department harboured a negative attitude towards the elephants and that 'the total destruction of the elephants was advocated in some quarters' during the 1920s because of the considerable damage they caused to State Blackwood plantings.8 Later, Carter11,55 reported the killing of four elephants between 1940 and 1970 and found the remains of a young elephant that had apparently been shot.

Several advocates of the illegal killing hypothesis argued that protection required more effort than mere declaration of protection, such as physical protection on the ground or fencing the elephants.10,11,14,52,53 The Knysna elephants' crop-raiding excursions10,11,52,53 often made headlines56-59. A major concern was that landowners shot at the elephants to chase them off their land and that these injured animals died only later of their injuries.9,11 In 1976, a local newspaper60 reported several requests to the Knysna Department of Forestry to destroy a damage-causing elephant. In addition, indirect and long-lasting effects of traumatic events, such as poaching or attempted poaching, have been reported elsewhere61 and include social fragmentation, potentially higher calf mortalities and lowered reproductive success.

Similarly, it was suggested that mere declaration of protection of the AENP elephants, with the proclamation of the park in 1931, did not lead to a recovery of the population as wandering elephants were shot on neighbouring farms.62 Reduction in elephant mortality and population recovery was only realised by erecting a boundary elephant-proof fence 23 years after park proclamation.53,62 Whitehouse and Hall-Martin63 identified the loss of the founder population's sexually mature bulls, between 1932 and 1940 as another factor that caused the initial slow growth rate of AENP's elephant population. The remaining young bulls reached sexual maturity by 1946, after which the population started its recovery.62,63

The available evidence highlighted here does not allow for a robust evaluation of the illegal killing hypothesis. However, it is likely that some illegal killing contributed to the slow demise of the Knysna elephants.

 

The stochastic founder hypothesis

Demographic stochasticity is a fluctuation in a population's growth rate caused by chance independent events of individual mortality and reproduction.13,64 With regard to extinction risk, small populations are particularly vulnerable to demographic stochasticity.13,64 The stochastic founder hypothesis suggests that after protection, the small population size and structure of the Knysna elephants exposed them to demographic stochasticity.

Between 1920 and 1970, it was estimated that four cows of breeding age were present in the Knysna elephant population.17 Forestry scientists argued that more than the observed two calves should therefore have been present if breeding was normal and suboptimal habitat did not reduce fertility.17 However, available information on the Knysna elephant population size, structure and individual life histories is vague or lacking. Between 1920 and 1970, a number of surveys recorded only one or two adult cows8,9,52, while Carter's11 survey concluded the presence of three adult cows (Table 1). The assumption of four sexually mature cows present during this time17 may therefore be an overestimate. In addition, even if there were four adult cows between 1920 and 1970, not all of them may have been fertile.

The differences between the Knysna and AENP elephants' founder populations lend credibility to the stochastic founder population hypothesis by illustrating how the Knysna population's small size and structure likely enhanced chance events that determined its fate. The Knysna elephant founder population consisted of 1-4 adult cows of unknown reproductive status, whereas the AENP founder population consisted of six sexually mature adult cows.63 By 1935/1936, eight sexually mature cows were present and eight calves were born during this time.63

Another difference between the populations is that the AENP cows seemed to have existed as one social group63 whereas the Knysna elephants were mostly sighted in small groups, containing only one adult cow and her offspring8,11,19,52. Such minimal group sizes may have contributed to the high calf mortality reported for the Knysna population.7-10,52,53 Elephants live in matriarchal societies consisting of family units of related adult females and their calves66,67 in which allomothering enhances survivorship68. One can therefore speculate that if there were sexually mature bulls and cows present between 1920 and the late 1900s, and the cows were mostly split into small groups consisting of an adult cow and her calf, the lack of allomothering may have played a significant role in reduced calf survival. Additionally, small group sizes may cause higher stress levels in African elephant cows which subsequently could lead to lowered reproductive outputs.61

It is highly likely that demographic stochasticity played a role in the inability of the small founder Knysna elephant population to recover after protection had been afforded.

 

Synthesis

Historical accounts illustrate how the southern Cape elephants were decimated by humans in the more open areas outside the afro-temperate forests, with the survivors taking up refuge in the forests during the late 1700s and 1800s. The elephant range thus decreased from a diverse array of habitats to only two habitat types: the afro-temperate forest and the surrounding fynbos. Ever-increasing human development eventually confined these elephants to the forests and isolated them from previously available habitat types. Range restriction - being one of the predictions of the refugee hypothesis - was thus realised.

Why the small surviving group of elephants in the Knysna forest never recovered, even after being afforded protection through their declaration of Royal Game in 1908, is less clear. Most of the scientific undertakings attempted to answer this question by linking habitat quality and population fitness by using density estimations obtained during the 1900s. Apart from the unreliability of the Knysna elephant density figures52, density can be a misleading indicator of habitat quality without demographic data to validate it18,69. The importance of demographic data in understanding processes that influence elephant populations has been clearly illustrated.70 In addition, habitat quality has been assessed in terms of food quality only, and other habitat aspects, for example, the availability of areas for socialising, that may be important to elephant, have been ignored. In light of this, we argue that the published works to date are too weak to link habitat quality to fitness, and the refugee hypothesis can thus not be eliminated.

Records of conflict between humans and the small surviving group of elephants on land neighbouring the Knysna forests suggest that landowners occasionally shot at elephants. In addition, some locals were of the opinion that the Forestry Department, in charge of the elephants' protection, harboured a negative attitude towards the elephants at the time. Besides the recorded Major Pretorius hunt, which saw five elephants killed in 1920, and the killing of a bull in 1971 by the Forestry Department, no records of killings are available. In addition, once again, demographic data are lacking. The illegal killing hypothesis can therefore not be eliminated.

The comparative records of the AENP and Knysna elephant founder populations' group structures reflect on potential stochastic effects. The small size and fragmented structure of the founder population may have played a significant role in the population decline, exacerbated by human disturbances such as illegal killings. We can thus not eliminate the stochastic effect hypothesis.

The results suggest that the failure of Knysna elephants to recover result from synergistic mechanisms.71 After the decimation of the southern Cape population in the 1700 and 1800s, the surviving population experienced a range restriction and took up refuge in the forests. Recovery of this refugee population was challenged because the habitat was sub-optimal. Conflict with humans, including illegal killings, most likely imposed an additional stressor on recovery. It is likely that small population stochastic effects accentuated the consequences of illegal killing and suboptimal habitats.

The Knysna elephant population exhibits similarities to other wildlife populations identified as refugee populations.18,72 Individuals of these refugee populations elsewhere had no access to historically optimal habitats and were subsequently managed and confined to suboptimal habitats. In these cases, population fitness was reduced with consequent declines in numbers. A major conservation risk is when authorities actively manage such populations under the false perception that the focal population occupies suitable habitats. Such perceptions restrict the development of appropriate mitigating management strategies.18

Determining the Knysna elephants' refugee status would therefore be a crucial and responsible consideration for their future short- and long-term management planning. The challenge, however, is the limited demographical data available as illustrated throughout this review. To overcome this challenge, we propose that an alternative approach be to investigate how the southern Cape elephants used the landscape before human barriers denied them the choice and access to more suitable habitat. The estuarine lake system, which has a higher soil nutrient status compared to the forest and fynbos habitats73 and which occurs along the southern Cape coast only 15-30 km south of the elephants' current range, could potentially be a more suitable habitat. These lake systems became cut-off from the current elephant range by farmlands, a national highway and towns. A scientific investigation into the historical southern Cape elephant population's seasonal habitat use patterns and potential diet shifts could be undertaken by analysing the stable isotopes of elements such as carbon, nitrogen and oxygen along ivory growth trajectories74 and the Knysna elephant population refugee status can thereby be robustly tested.

 

Management implications

The synergistic mechanisms of decline that we highlight have three implications for management. If elephant presence is desirable in the Knysna forest, the recovery of elephants requires innovative elephant reintroductions from elsewhere, as the forests have been isolated from potential elephant source populations for a long time and constructed barriers will prevent natural colonisation. A primary challenge is how to reintroduce elephants given the failure of the previous reintroduction.16,17 However, reintroductions will overcome the predictions of the stochastic small population hypothesis. Furthermore, the persistence of elephants will require regular supplementary introductions to overcome the predictions of the suboptimal habitat element of the refugee hypothesis. Additionally, the availability of optimal habitat types, close to the Knysna elephant range, and the possibilities of range expansion, should be investigated. In addition, authorities will need to implement effective anti-poaching and law enforcement programmes to overcome the predictions of the illegal killing hypothesis.

 

Authors' contributions

L.M.: Conceptualisation, data collection, writing the initial draft, writing revisions, preparing the submitted draft. S.M.F.: Conceptualisation, writing revisions. A.G. and D.Z.: Writing revisions. G.I.H.K.: Conceptualisation, writing the initial draft, writing revisions, project leadership.

 

References

1.Robson AS, Trimble MJ, Purdon A, Young-Overton KD, Pimm SL, Van Aarde RJ. Savanna elephant numbers are only a quarter of their expected values. PLoS ONE. 2017;12(4), e0175942, 14 pages. https://doi.org/10.1371/journal.pone.0175942        [ Links ]

2.Chase MJ, Schlossberg S, Griffin CR, Bouché PJ, Djene SW, Elkan PW, et al. Continent-wide survey reveals massive decline in African savannah elephants. PeerJ. 2016;4, e2354, 24 pages. https://doi.org/10.7717/peerj.2354        [ Links ]

3.Hall-Martin AJ. Distribution and status of the African elephant Loxodonta africana in South Africa, 1652-1992. Koedoe. 1992;35(1):65-88. https://doi.org/10.4102/koedoe.v35i1.390        [ Links ]

4.Kerley GIH, Pressey RL, Cowling RM, Boshoff AF, Sims-Castley R. Options for the conservation of large and medium sized mammals in the Cape Floristic Region hotspot, South Africa. Biol Conserv. 2003;112:169-190. https://doi.org/10.1016/S0006-3207(02)00426-3        [ Links ]

5.Boshoff AF, Kerley GI, Cowling RM. Estimated spatial requirements of the medium-to large-sized mammals, according to broad habitat units, in the Cape Floristic Region, South Africa. Afr J Range For Sci. 2002;19:29-44. https://doi.org/10.2989/10220110209485772        [ Links ]

6.Roche CJ. 'The Elephants at Knysna' and 'The Knysna Elephants': From Exploitation to conservation: Man and elephants at Knysna 1856-1920 [Hons thesis]. Cape Town: University of Cape Town; 1996.         [ Links ]

7.Phillips JF. The Knysna elephant: A brief note on their history and habits. S Afr J Sci. 1925;22:287-293.         [ Links ]

8.Dommisse EJ. The Knysna elephants, historical sketch of a world-famous herd. Afr Wildl. 1951;5:195-199.         [ Links ]

9.Woods DH. Report on the Bernard Carp Knysna elephant expedition. Afr Wildl. 1952;6:6-7.         [ Links ]

10.Hey D. The elephants of the Knysna forest. Afr Wildl. 1962;16:101-108.         [ Links ]

11.Carter B. Knysna elephant survey, February 1969-January 1970. Port Elizabeth: Wild Life Protection and Conservation Society of South Africa, Eastern Province Branch; 1970.         [ Links ]

12.Eggert LS, Patterson G, Maldonado JE. The Knysna elephants: A population study conducted using faecal DNA. Afr J Ecol. 2007;46:19-23. https://doi.org/10.1111/j.1365-2028.2007.00794.x        [ Links ]

13.Caughley G. Directions in conservation biology. J Anim Ecol. 1994;63:215-244. https://doi.org/10.2307/5542        [ Links ]

14.Greig JC. Are the Knysna elephants a distinct race? Afr Wildl. 1982;36:210-215.         [ Links ]

15.Koen JH, Hall-Martin AJ, Erasmus T. Macro nutrients in plants available to the Knysna, Addo, and Kruger National Park elephants. S Afr J Wildl Res. 1988;18:69-71.         [ Links ]

16.Mackay M. The Knysna elephants and their forest home. Knysna: Wildlife and Environment Society of South Africa; 1996.         [ Links ]

17.Seydack AH, Vermeulen C, Huisamen J. Habitat quality and the decline of an African elephant population: Implications for conservation. S Afr J Wildl Res. 2000;30:34-42.         [ Links ]

18.Kerley GIH, Kowalczyk R, Cromsigt JP. Conservation implications of the refugee species concept and the European bison: King of the forest or refugee in a marginal habitat? Ecography. 2012;35:519-529. https://doi.org/10.1111/j.1600-0587.2011.07146.x        [ Links ]

19.Carter B. The elephants of Knysna. Cape Town: Purnell; 1971.         [ Links ]

20.Fairall N. The Knysna elephants - a non-issue. Afr Wildl. 1982;36:197.         [ Links ]

21.Koen JH. Trace elements and some other nutrients in the diet of the Knysna elephants. S Afr J Wildl Res. 1988;18:109-110.         [ Links ]

22.Smithers RHN. The mammals of the southern African subregion. Pretoria: University of Pretoria; 1983.         [ Links ]

23.Granados A, Weladji RB, Loomis MR. Movement and occurrence of two elephant herds in a human-dominated landscape, the Bénoué Wildlife Conservation Area, Cameroon. Trop Conserv Sci. 2012;5:150-162. https://doi.org/10.1177/194008291200500205        [ Links ]

24.Jachowski DS, Slotow R, Millspaugh JJ. Physiological stress and refuge behavior by African elephants. PLoS ONE. 2012;7, e31818, 11 pages. https://doi.org/10.1371/journal.pone.0031818        [ Links ]

25.Gunn J, Hawkins D, Barnes RF, Mofulu F, Grant RA, Norton GW. The influence of lunar cycles on crop-raiding elephants; evidence for risk avoidance. Afr J Ecol. 2013;52:129-137. https://doi.org/10.1111/aje.12091        [ Links ]

26.Murai M, Ruffler H, Berlemont A, Campbell G, Esono F, Agbor A, et al. Priority areas for large mammal conservation in Equatorial Guinea. PLoS ONE. 2013;8, e75024, 13 pages. https://doi.org/10.1371/journal.pone.0075024        [ Links ]

27.Essop MF, Hall-Martin AJ, Harley EH. Mitochondrial DNA analysis of two southern African elephant populations. Koedoe. 1996;39:85-88. https://doi.org/10.4102/koedoe.v39i1.284        [ Links ]

28.Boshoff AF, Landman M, Kerley GIH. Filling the gaps on the maps: Historical distribution patterns of some larger mammals in part of southern Africa. Trans R Soc S Afr. 2016;71:23-87. https://doi.org/10.1080/0035919X.2015.1084066        [ Links ]

29.Skead CJ. Historical incidence of the larger land mammals in the broader Western and Northern Cape. 2nd ed. Port Elizabeth: Centre for African Conservation Ecology, Nelson Mandela Metropolitan University; 2011.         [ Links ]

30.Rookmaaker LC. The zoological exploration of southern Africa 1650-1790. Rotterdam: AA Balkema; 1989.         [ Links ]

31.Elephant again. The George and Knysna Herald. 1883 May 23; no. 74:3 (col. 3).         [ Links ]

32.Carruthers J, Boshoff AF, Slotow R, Biggs H, Avery G, Matthews W. The elephant in South Africa: History and distribution. In: Scholes RJ, Mennell KG, editors. Elephant management: A scientific assessment for South Africa. Johannesburg: Wits University Press, 2008; p. 23-83.         [ Links ]

33.Skinner JD, Chimimba CT. The mammals of the southern African sub-region. Cambridge: Cambridge University Press; 2005. https://doi.org/10.1017/CBO9781107340992        [ Links ]

34.Van Daalen JC. Distinguishing features of forest species on nutrient-poor soils in the Southern Cape. Bothalia. 1984;15:29-39. https://doi.org/10.4102/abc.v15i1/2.1123        [ Links ]

35.Koen JH. A study of the distribution, population composition, movements and feeding of the Knysna elephants Loxodonta africana africana (Blumebach 1797). Knysna: Forestry Department, 1984.         [ Links ]

36.Robbins CT. Wildlife feeding and nutrition. New York: Academic Press; 1983.         [ Links ]

37.Illius AW, Gordon IJ. Modelling the nutritional ecology of ungulate herbivores: Evolution of body size and competitive interactions. Oecologia. 1992;89:428-434. https://doi.org/10.1007/BF00317422        [ Links ]

38.Olff H, Ritchie ME, Prins HH. Global environmental controls of diversity in large herbivores. Nature. 2002;415:901-904. https://doi.org/10.1038/415901a        [ Links ]

39.Fritz H, Duncan P, Gordon IJ, Illius AW. Megaherbivores influence trophic guilds structure in African ungulate communities. Oecologia. 2002;131:620-625. https://doi.org/10.1007/s00442-002-0919-3        [ Links ]

40.Holdø RM, Dudley JP, McDowell LR. Geophagy in the African elephant in relation to availability of dietary sodium. J Mammal. 2002;83:652-664. https://doi.org/10.1644/1545-1542(2002)083<0652:GITAEI>2.0.CO;2        [ Links ]

41.Matthews WS, Van Wyk AE, Van Rooyen N, Botha GA. Vegetation of the Tembe Elephant Park, Maputaland, South Africa. S Afr J Bot. 2001;67:573-594. https://doi.org/10.1016/S0254-6299(15)31188-1        [ Links ]

42.Weir JS. Spatial distribution of elephants in an African National Park in relation to environmental sodium. Oikos. 1972;23:1-13. https://doi.org/10.2307/3543921        [ Links ]

43.Rode KD, Chiyo PI, Chapman CA, McDowell LR. Nutritional ecology of elephants in Kibale National Park, Uganda, and its relationship with crop-raiding behaviour. J Trop Ecol. 2006;22:441-449. https://doi.org/10.1017/S0266467406003233        [ Links ]

44.Kabigumila J. Feeding habits of elephants in Ngorongoro Crater, Tanzania. Afr J Ecol. 1993;31:156-164. https://doi.org/10.1111/j.1365-2028.1993.tb00528.x        [ Links ]

45.De Boer WF, Ntumi CP, Correia AU, Mafuca JM. Diet and distribution of elephant in the Maputo Elephant Reserve, Mozambique. Afr J Ecol. 2000;38:188-201. https://doi.org/10.1046/j.1365-2028.2000.00243.x        [ Links ]

46.Radloff FGT. The ecology of large herbivores native to the coastal lowlands of the Fynbos Biome in the Western Cape, South Africa [PhD thesis]. Stellenbosch: Stellenbosch University; 2008.         [ Links ]

47.Stamps JA, Swaisgood RR. Someplace like home: Experience, habitat selection and conservation biology. Appl Anim Behav Sci. 2007;102:392-409. https://doi.org/10.1016/j.applanim.2006.05.038        [ Links ]

48.Davis JM, Stamps JA. The effect of natal experience on habitat preferences. Trends Ecol Evol. 2004;19:411-416. https://doi.org/10.1016/j.tree.2004.04.006        [ Links ]

49.Pinter-Wollman N. Spatial behaviour of translocated African elephants (Loxodonta africana) in a novel environment: using behaviour to inform conservation actions. Behaviour. 2009;146:1171-1192. https://doi.org/10.1163/156853909X413105        [ Links ]

50.Fernando P, Leimgruber P, Prasad T, Pastorini J. Problem-elephant translocation: translocating the problem and the elephant? PLoS ONE. 2012;7, e50917, 9 pages. https://doi.org/10.1371/journal.pone.0050917        [ Links ]

51.Lee PC, Moss CJ. Early maternal investment in male and female African elephant calves. Behav Ecol Sociobiol. 1986;18:353-361. https://doi.org/10.1007/BF00299666        [ Links ]

52.Fraser A. Report: Survey of elephant population of the Knysna Forest. Knysna: South African National Park; 1957.         [ Links ]

53.Hall-Martin A. Elephant survivors. Oryx. 1980;15:355-362. https://doi.org/10.1017/S0030605300028830        [ Links ]

54.Lydekker R. The ears as a race-character in the African elephant. Proc Zool Soc Lond. 1907;77:380-403. https://doi.org/10.1111/j.1096-3642.1907.tb01824.x        [ Links ]

55.Carter B. Counting the Knysna elephants. Afr Wildlife. 1969;23:279-286.         [ Links ]

56.Elephants again. The George and Knysna Herald. 1957 February 01; no. 3830:6 (col. 7).         [ Links ]

57.Olifante eis eerste slagoffer [Elephants claim first victim]. The George and Knysna Herald. 1963 June 21; no. 3070:4 (col. 5). Afrikaans.         [ Links ]

58.No elephant hunt at Knysna. The George and Knysna Herald. 1964 September 11;1 (col. 3).         [ Links ]

59.How to get rid of an elephant. The George and Knysna Herald. 1970 July 17;1 (col. 5).         [ Links ]

60.Request to kill Knysna elephant. EP Herald. 1967 October 20.         [ Links ]

61.Gobush KS, Mutayoba BM, Wasser SK. Long-term impacts of poaching on relatedness, stress physiology, and reproductive output of adult female African elephants. Conserv Biol. 2008;22:1590-1599. https://doi.org/10.1111/j.1523-1739.2008.01035.x        [ Links ]

62.Whitehouse AM. Tusklessness in the elephant population of the Addo Elephant National Park, South Africa. J Zool. 2002;257:249-254. https://doi.org/10.1017/S0952836902000845        [ Links ]

63.Whitehouse AM, Hall-Martin AJ. Elephants in Addo Elephant National Park, South Africa: Reconstruction of the population's history. Oryx. 2000;34:46-55. https://doi.org/10.1017/S0030605300030891        [ Links ]

64.Lee AM, Sæther BE, Engen S. Demographic stochasticity, allee effects, and extinction: The influence of mating system and sex ratio. Am Nat. 2011;177:301-313. https://doi.org/10.1086/658344        [ Links ]

65.Woods DH. The Knysna elephants. Afr Wildlife. 1958;12:118-124.         [ Links ]

66.Moss CJ. The demography of an African elephant (Loxodonta africana) population in Amboseli, Kenya. J Zool. 2001;255:145-156. https://doi.org/10.1017/S0952836901001212        [ Links ]

67.Archie EA, Moss CJ, Alberts SC. The ties that bind: Genetic relatedness predicts the fission and fusion of social groups in wild African elephants. Proc R Soc Lond B Biol Sci. 2006;273:513-522. https://doi:10.1098/rspb.2005.3361        [ Links ]

68.Lee PC. Allomothering among African elephants. Anim Behav. 1987;35:278-291. https://doi.org/10.1016/S0003-3472(87)80234-8        [ Links ]

69.Van Horne B. Density as a misleading indicator of habitat quality. J Wildl Manage. 1983;47:893-901. https://doi.org/10.2307/3808148        [ Links ]

70.Wittemyer G, Daballen D, Douglas-Hamilton I. Comparative demography of an at-risk African elephant population. PLoS ONE. 2013;8, e53726, 10 pages. https://doi.org/10.1371/journal.pone.0053726        [ Links ]

71.Brook BW, Sodhi NS, Bradshaw CJ. Synergies among extinction drivers under global change. Trends Ecol Evol. 2008;23:453-460. https://doi.org/10.1016/j.tree.2008.03.011        [ Links ]

72.Lea JM, Kerley GI, Hrabar H, Barry TJ, Shultz S. Recognition and management of ecological refugees: A case study of the Cape mountain zebra. Biol Conserv. 2016;203:207-215. https://doi.org/10.1016/j.biocon.2016.09.017        [ Links ]

73.Whitfield AK, Lubke RA. Estuarine and coastal lake ecology. In: Lubke RA, De Moor I, editors. Field guide to the eastern and southern Cape coasts. Cape Town: University of Cape Town Press; 1998. p. 216-232.         [ Links ]

74.Codron J. Annals of ivory: Perspectives on African elephant Loxodonta africana (Blumenbach 1797) feeding ecology from a multi-decadal record [PhD thesis]. Cape Town: University of Cape Town; 2008.         [ Links ]

75.Moolman L, De Morney MA, Ferreira SM, Ganswindt A, Poole JH, Kerley GI. And then there was one: A camera trap survey of the declining population of African elephants in Knysna, South Africa. Afr J Wildl Res. 2019;49(1):16-26.         [ Links ]

 

 

Correspondence:
Lizette Moolman
Lizette.moolman@sanparks.org

Received: 23 Mar. 2018
Revised: 29 Sep. 2018
Accepted: 24 Jan. 2019
Published: 27 Mar. 2019

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