Abstract Introduction Study area Methods Results and discussion Acknowledgements References About the Author(s) Hendrik Sithole Scientific Services, South African National Parks, Hadison Park, Kimberley, South Africa School of Animal, Plant and Environmental Sciences, University of the Witwatersrand, Johannesburg, South Africa Nolubabalo Tantsi Department of Agriculture and Rural Development, Provincial Government of South Africa, Johannesburg, South Africa Hugo Bezuidenhout Scientific Services, South African National Parks, Hadison Park, Kimberley, South Africa Applied Behavioural Ecology and Ecosystem Research Unit, University of South Africa, Pretoria, South Africa Thinandavha C. Munyai School of Life Science, University of KwaZulu-Natal, Durban, South Africa Lufuno Munyai Scientific Services, South African National Parks, Hadison Park, Kimberley, South Africa Citation Sithole, H., Tantsi, N., Bezuidenhout, H., Munyai T.C. & Munyai, L., 2020, ‘Reconnaissance of epigeal ants at the degraded and control sites of Mountain Zebra and Mokala National Parks’, Koedoe 62(1), a1542. https://doi.org/10.4102/koedoe.v62i1.1542 Short Communication Reconnaissance of epigeal ants at the degraded and control sites of Mountain Zebra and Mokala National Parks Hendrik Sithole, Nolubabalo Tantsi, Hugo Bezuidenhout, Thinandavha C. Munyai, Lufuno Munyai Received: 03 May 2018; Accepted: 08 Mar. 2020; Published: 25 May 2020 Copyright: © 2020. The Author(s). Licensee: AOSIS. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract South African National Parks (SANParks) is implementing rehabilitation projects in parks where acquired lands have degrees of degradation. Such parks need to have empirical data to determine the degree of degradation and the success of the projects. We sampled epigeal ants at degraded and control sites in Mountain Zebra and Mokala National Parks to acquire the empirical data. With the data, our main aims were to: 1) determine the impact of degradation on the ant community; 2) determine if the rehabilitation period influences the difference between the degraded and control sites; and, 3) identify the degradation that affected the ant community the most. The majority of the degraded sites had lower abundance, species richness, Shannon-Wiener Diversity, common- and exclusive-species than their respective control sites. All the degraded sites had a lower abundance of ants compared to their respective controls. The majority of the degraded sites had lower species richness, higher Shannon-Weiner Diversity Index and higher ant species dominance than their respective controls. The rehabilitation periods differently influenced the difference between the degraded and control sites. Degraded sites that had undergone longer rehabilitation times had lower dissimilarity to their respective controls, while a degraded site with shorter rehabilitation period was very different to its control. Ploughing appears to have longer lasting degradation-impact on ant communities than herbicides applications. A site with ploughing degradation was very dissimilar to its control while sites with chemical degradation had lower disparities to their respective controls. Different degradation activities, therefor, affect ant recovery differently. Conservation implications: Attention should be paid to the type of degradations that are at the lands identified for expanding the conservation areas. Some of these degradations seem persistent and slow to rehabilitate. Variety of organisms (such as ants in this case) should be included when determining the degradation status of a conservation land. Keywords: disparity; indicator species; rehabilitation age; degradation method; conservation; ecology. Introduction Habitat loss is the decline of ecological (or environmental) area (or community) by any action resulting in unfavourable conditions for species to complete their lifecycles (Galvin 2007). Habitat loss is one of the main drivers for the decline of especially endemic species in South Africa as well as globally (International Union for Conservation of Nature (IUCN) 2015). To preserve the indigenous habitats that are within its jurisdiction, the South African National Parks (SANParks) is implementing rehabilitation projects where varying degrees and types of habitat degradation occur (South African National Parks (SANParks) 2016). A reconnaissance was carried out in two SANParks, Mountain Zebra (MZNP) and Mokala (MoNP), to compare ant diversity and abundance in degraded and undisturbed control areas. Over-grazing, ploughing and eradication of alien species lead to degradation in MZNP, whilst chemical treatment to control woody plant species was the main factor in MoNP. We chose to use ants as they often respond temporally and spatially to degradation (Gollan et al. 2011). They exhibit relatively low mobility or dispersion within their habitats (Barrow & Parr 2008), and interact with different organisms at different trophic and symbiotic levels (Agosti, Schultz & Majer 2000; Hölldobler & Wilson 1990). Sampling ants is also relatively cheap (McGeoch et al. 2011). The main aims for this study are as follows: (1) To determine whether degradation affects the ant communities; this was conducted by comparing ant composition diversity between degraded and control sites of a specific locality. (2) To determine whether rehabilitation periods influence ant communities by comparing the specific biodiversity index disparity between the localities with varying rehabilitation periods. (3) To identify which of these degradation activities impacted most on ant communities by comparing the specific biodiversity index disparity between the localities. Study area The MZNP (32.20500° S, 25.45000° E) is situated in the Eastern Cape province of South Africa (Figure 1). Its vegetation consists of a mixture of dwarf shrubs and grasses (Bezuidenhout & Brown 2008). The area receives late summer rain, with the highest rainfall recorded in March and the lowest in June. Average temperature ranges from 0.5 °C to 28.4 °C (Bezuidenhout & Brown 2008). Three localities were selected in this park. The first locality was Groenfontein with the degraded site, at 32.215628° S, 25.119439° E, consisting of bare soil surface and debris left after clearance of the alien plant species Populus canescens. The control site for this was at Groenfontein (32.21563° S, 25.11844° E), which had no history of any degradation. Its proximity to the degraded site and similar habitat makes it a valid control site. The second locality was Juriesdam. This degraded site, at 32.18846° S, 25.49268° E, suffered from sheep overgrazing with its undisturbed control site situated at 32.19030° S, 25.40922° E on a similar habitat (Brown & Bezuidenhout 2018; Van der Walt 1980). The third locality was uBejani. The degraded site, at 32.16859° S, 25.47663° E, was formally a ploughed field, and the undisturbed control site was situated at 32.17062° S, 25.46189° E. The proximity and habitat similarity between these sites make the site a valid control site. FIGURE 1: The map showing the localities where ants were sampled from both degraded and control sites in Mountain Zebra and Mokala National Parks. The MoNP (29.10350° S, 24.39410° E) is located in the Northern Cape province of South Africa. The dominant vegetation types are Kimberley Thornveld, Vaalbos Rocky Shrubland and Northern Upper Karoo (Bezuidenhout et al. 2015a) (Figure 1). The area receives late summer rain with the highest rainfall recorded in March and the lowest in June. The temperature ranges from −6.61 °C to 39.95 °C (Bezuidenhout et al. 2015a). The two localities that were selected were Windpomp and Puntberg (Figure 1), where bush densification of Senegalia mellifera (Swarthaak) was treated chemically (Bezuidenhout, Kraaij & Baard 2015b). The degraded site of Windpomp was located at 29.11187° S, 24.37244° E and the control site was at 29.11069° S, 24.37556° E. The degraded site at Puntberg was situated at 29.13396° S, 24.31461° E with the control site at 29.14880° S, 24.32222° E. Methods Twenty pitfall traps (100 mL plastic cups), each containing 50 mL of 50% propylene glycol–water solution (Adis 1979), were placed at the centre of each site in a grid of 5 × 4 rows (each 10 m apart) for 96 hours. Ants were sampled in November 2015 at the MZNP sites, and in February 2016 for the MoNP sites. Only female workers were then identified to genus level using the keys of Bolton (1994). The morphospecies of the identified specimens from each genus were then given a code based on their external morphological characteristics (viz. body sculptures, body colouring, hair/setae colour, hair/setae shape and petiole shape). All samples were kept at Scientific Services, Kimberley, SANParks, for the future reference. The biodiversity indices used to determine the composition of ant communities from each site were abundance, species richness, dominant species (i.e. the most abundant) and similarity (Anderson et al. 2008; Dandan & Zhiwei 2007; Spellerberg & Fedor 2003). Sampled ant specimens and the morphospecies were counted to get the ant abundance and ant species richness for each site. The total abundance of all ant species for each site and the relative abundance of each ant species were calculated. The relative abundance of all ant species was ranked in decreasing order to get species that contributed ≥ 75% of the total abundance of each site. The Shannon–Wiener Index and Simpson’s Diversity Index were used to calculate the ant diversity per site (Spellerberg & Fedor 2003). Sorenson’s Coefficient (Dandan & Zhiwei 2007) was used to determine ant community similarities between the sites of each locality. The difference between the degraded and control sites of each locality, for each biodiversity index, was compared with its counterparts from other localities. The differences were given a score ranging from 1 (for the least difference) to 5 (for the highest difference) (Roux et al. 2002) for the following indices: abundance, species richness, Shannon–Wiener Diversity Index and Simpson’s Diversity Index. The scores for the dominant species were given 0 (where at least three of the five most abundant species at the degraded and control sites were of the same species – regardless of the order of their abundance at top five) or 1 (where at least three of the five most abundant species were different between the degraded and the control sites – regardless of the order of their abundance at top five). The scores for Sorenson’s Coefficient Index ranged from 1 (for a locality with the highest Sorenson’s Coefficient) to 5 (for the lowest Sorenson’s Coefficient). All the scores for each locality were then summed up and compared with other localities. Ethical considerations This article followed all ethical standards for a research without direct contact with human or animal subjects. Results and discussion All the degraded sites had lower abundance values than their controls (Figure 2), with the largest difference at Groenfontein and the least difference at Juriesdam (Figure 2, Table 1). FIGURE 2: Diversity indices of ants sampled on degraded and control sites from localities at the Mountain Zebra National Park and Mokala National Park. TABLE 1: Index values from the degraded and control sites of each locality and their disparity rankings relative to other localities. Species richness was lower at the degraded sites of Groenfontein, uBejani and Puntberg relative to their controls (Figure 2) but was higher at the degraded sites of Juriesdam. The species richness was similar at the degraded and control sites of Windpomp. The degraded and control sites of the uBejani locality had the most dissimilar species richness, whilst the degraded and control sites of the Windpomp locality were least dissimilar (Figure 2, Table 1). The Shannon–Wiener Diversity Index indicated that ant diversity was higher at the degraded sites of Groenfontein, Juriesdam, uBejani and Windpomp, and lowest at Puntberg (Figure 2). The largest Shannon–Wiener Diversity Index difference was at uBejani and the least difference was at Juriesdam (Figure 2, Table 1). The Simpson’s Index showed that Groenfontein, uBejani and Windpomp had higher dominance at the degraded sites, whilst the degraded sites of Juriesdam and Puntberg had lower dominance in relation to their control sites (Figure 2). The uBejani sites had the highest Simpson’s Index difference, whilst Puntberg sites had the least Simpson’s Index difference (Figure 2, Table 1). Although the degraded and control sites of most localities had similar dominating ant species (except Juriesdam and Windpomp) (Table 1), most of the ant species contributing ≥75% of the total abundance of the locality were less abundant (and in fewer traps) at the degraded sites (Table 2). TABLE 2: Species list of ants sampled from each locality with their abundance and indications stating their roles in dissimilarity contributions and exclusivity between the degraded and control sites. The low abundance and species richness at the degraded sites suggest that the treatments applied in the habitats were not supportive to ant communities (Table 1). Ant sampling should be included in the methodology used to assess achievement of the aims of rehabilitation interventions. These data and the sampling methodology can also be used in monitoring projects to assess the temporal trends of ant communities to assess rehabilitation actions. Ants are dominant in the terrestrial ecosystems based on their biomass, interactions with other organisms, their roles in the ecosystem and their response to disturbances, as suggested by this study. We suggest that the lower biodiversity indices from the degraded sites (Figure 2) are driven by the disturbance (or even the diminution) of microhabitats. These disturbances may have altered the effects of driving factors (such as temperature and humidity) to levels beyond the tolerance of some species (Gibb et al. 2015; Hölldobler & Wilson 1990). These changes may have favoured species that are able to adapt to harsher conditions, for instance, Ocymyrmex species (Hölldobler & Wilson 1990; Marsh 1985; Sommer et al. 2013). Ocymyrmex sp. 1 was more abundant at degraded sites of all the localities, except Juriesdam, where it was not recorded (Table 2). The abundance of Ocymyrmex species, where it occurs, could further be used as a general indicator that determines the progress of rehabilitation actions (Table 2). This could be performed by comparing the abundance disparities of Ocymyrmex sp. 1 at a degraded site relative to its control, or by temporally comparing its abundance in a specific degraded site to determine the trend followed by abundance. The lower ant abundance at all the degraded sites, and the lower species richness at most of the degraded sites (Figure 2), could have affected the important myrmecophile roles at these sites as there could be relatively fewer ants to fulfil their roles in ecosystems in both intraspecific and interspecific symbioses such as competition, mutualism, parasitism and feeding behaviours (Hölldobler & Wilson 1990). Therefore, this could have affected organisms that rely on myrmecophile relationships (positive interactions between ants and other organisms) (Hölldobler & Wilson 1990). Differences between degraded and control sites suggest that time plays an important role in the rehabilitation process. Sites that had been recently rehabilitated, such as Groenfontein, had the highest overall differences, whilst the ones that had been rehabilitated before, such as Windpomp and Puntberg, had the lowest overall (Table 1) differences. The narrower disparities at Puntberg and Windpomp could be attributed to improved habitat because of longer recovery time (Table 1). This follows data findings of Andersen, Hoffmann and Somes (2003), who also found ants recover better with increasing rehabilitation time. We therefore anticipate that in the future the differences in younger rehabilitated localities would decrease. In addition to the time of rehabilitation, the type of degradation also influences the recovery (Vasconcelos 1999). uBejani site has the longest rehabilitation time but had the second highest overall differences between its sites (Table 1). We relate this difference to the ploughing that took place at the degraded site. Chan (2001) reported that ploughing disturbs the soil profile and its associated organisms. This again could have had an impact on the ant community by affecting their myrmecophily association with the soil, other arthropods and plant species (Agosti et al. 2000; Hölldobler & Wilson 1990). We anticipate there will be a slower narrowing of differences at uBejani relative to other localities because of the type of degradation it experienced. The type of degradation can sometimes have no direct impact on ants, as was seen at Puntberg, Juriesdam and Windpomp which have the least disparities between the sites and controls (see overall score in Table 1). The degraded sites at Puntberg and Windpomp experienced chemical degradations, mostly with Tebuthiuron as the active ingredient (Bezuidenhout et al. 2015b) to eradicate woody plant species. As this chemical is systemic and absorbed through the roots (Blaise & Harwood 1991), it may not have been in direct contact with epigeal ants. The chemical may, therefore, had little impact on the ants. We are unsure whether the difference in these localities would remain relatively low because Johnsen and Morto (1989) reported that the concentration of Tebuthiuron and its depth in the soil changes under different rainfall conditions. It may be possible to show this by samplings during different rainfall conditions. Because this is only a preliminary study conducted during local drought conditions, we recommend further sampling when the rainfall is back to previous averages. We hope also that additional samplings could verify whether the differences still hold for all different sampled degradations. In conclusion, we suggest that environmental authorities should consider the importance of the degradation types when acquiring lands for expanding conservation areas with consideration for brother organisms. As some of these degradation types seem to be persistent and take longer and more effort to be rehabilitated whilst others need lesser effort. They should also consider including different organisms when determining the degradation condition of the concerned conservation land. Including different organisms when assessing such land would inform the management as to how degraded is that land, in general, and therefore make the decision based on the assessment that would include different avenues. Acknowledgements SANParks and Biodiversity Social Projects in SANParks provided funding and manpower for this project. The following people contributed immensely towards collecting data for this article: Clodene Ackerman, Pulane Daemane, Letlhogonolo Kotsokoane, Abel Matsapula, Phindile Mbele, Kelebogile Mohudi, Spencely Motloung, Mazwi Mthethwa, Shadi Ndouvhada, Lucky Ramabulana, Bruce Taplin and Nosidima Vumindaba. Laboratory space to identify ant specimen was provided by the Arid Lands Node of the South African Environmental Observation Network (SAEON) in Kimberley. The authors would like to thank the referees who reviewed the article. Competing interests The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article. Authors’ contributions H.S. was the project leader and responsible for sampling design, project implementation, data analysis and article writing. N.T. was responsible for project implementation, data analyses and article writing. H.B. and T.C.M. were responsible for article writing. L.M. was responsible for sampling. Funding information SANParks and Biodiversity Social Projects in SANParks provided funding and manpower for this project. Data availability statement Data sharing is not applicable to this article as no new data were created or analysed in this study. Disclaimer The views and opinions expressed in this article are those of the authors and do not necessarily reflect the official policy or position of any affiliated agency of the authors. References Adis, J., 1979, ‘Problems of interpreting arthropod sampling with pitfall traps’, Zoologischer Anzeiger 202, 117–184. Agosti, D., Schultz, T. & Majer, J.D. (eds.), 2000, Ants, Smithsonian Institution Press, Washington, DC. Andersen, A.N., Hoffmann, B.D. & Somes, J., 2003, ‘Ants as indicators of minesite restoration: Community recovery at one of eight rehabilitation sites in central Queensland’, Ecological Management & Restoration 4(s1), S12–S19. https://doi.org/10.1046/j.1442-8903.4.s.2.x Anderson, M., Gorley, R. & Clarke, K.P., 2008, PERMANOVA+ for PRIMER: Guide to software and statistical methods, PRIMER-E, Plymouth. Barrow, L. & Parr, C.L., 2008, ‘A preliminary investigation of temporal patterns in semi-arid ant communities: Variation with habitat type’, Austral Ecology 33(5), 653–662. https://doi.org/10.1111/j.1442-9993.2008.01832.x Bezuidenhout, H. & Brown, L.R., 2008, ‘Vegetation description of the Doornhoek section of the Mountain Zebra National Park (MZNP), South Africa’, Koedoe 50(1), 82–92. https://doi.org/10.4102/koedoe.v50i1.142 Bezuidenhout, H., Bradshaw, P.L., Bradshaw, M. & Zietsman, P.C., 2015a, ‘Landscape units of Mokala National Park, Northern Cape Province, South Africa’, Navorsinge van die Nasionale Museum Bloemfontein 31, 1–27. Bezuidenhout, H., Kraaij, T. & Baard, J., 2015b, ‘Persistent effects of chemicals used to control shrub densification in semi-arid Savanna’, Earth Science Research 4(1), 31–39. https://doi.org/10.5539/esr.v4n1p31 Blaise, C. & Harwood, M., 1991, ‘Ecotoxicological assessment of Tebuthiuron – A substituted urea class herbicide’, Revue des Sciences de l’eau/Journal of Water Science 4(1), 121–134. https://doi.org/10.7202/705093ar Bolton, B., 1994, Identification guide to the ant genera of the world, Harvard University Press, Cambridge. Brown, L.R. & Bezuidenhout, H., 2018, ‘Ecosystem description and diversity of the Jurisdam-Seekoegat sections of the Mountain Zebra National Park, South Africa’, South African Journal of Botany 118, 166–178. https://doi.org/10.1016/j.sajb.2018.07.013 Chan, K.Y., 2001, ‘An overview of some tillage impacts on earthworm population abundance and diversity – Implications for functioning in soils’, Soil and Tillage Research 57(4), 179–191. https://doi.org/10.1016/S0167-1987(00)00173-2 Dandan, Z. & Zhiwei, Z., 2007, ‘Biodiversity of arbuscular mycorrhizal fungi in the hot-dry valley of the Jinsha River, southwest China’, Applied Soil Ecology 37(1), 118–128. https://doi.org/10.1016/j.apsoil.2007.06.003 Galvin, K.A., 2007, Fragmentation in semi-arid and arid landscapes: Consequences for human and natural systems, Springer, Dordrecht. Gibb, H., Sanders, N.J., Dunn, R.R., Watson, S., Photakis, M., Abril, S. et al., 2015, ‘Climate mediates the effects of disturbance on ant assemblage structure’, Proceedings of the Royal Society B 282(1808), 20150418. https://doi.org/10.1098/rspb.2015.0418 Gollan, J.R, De Bruyn, L.L., Reid, N., Smith, D. & Wilkie, L., 2011, ‘Can ants be used as ecological indicators of restoration progress in dynamic environments? A case study in a revegetated riparian zone’, Ecological Indicator 11(6), 1517–1525. https://doi.org/10.1016/j.ecolind.2009.09.007 Hölldobler, B. & Wilson, E.O., 1990, The ants, Springer-Verlag, Berlin. International Union for Conservation of Nature (IUCN), 2015, The IUCN red list of threatened species, version 2015.1, viewed October 2016, from http://www.iucnredlist.org. Johnsen, T.N. & Morton, H.L., 1989, ‘Tebuthiuron persistence and distribution in some semiarid soils’, Journal of Environmental Quality 18(4), 433–438. https://doi.org/10.2134/jeq1989.00472425001800040006x Marsh, A.C., 1985, ‘Microclimatic factors influencing foraging patterns and success of the thermophilic desert ant’, Ocymyrmex Barbiger. Insectes Sociaux 32(3), 286–296. https://doi.org/10.1007/BF02224917 McGeoch, M.A., Sithole, H., Samways, M.J., Simaika, J.P., Pryke, J.S., Picker, M. et al., 2011, ‘Conservation and monitoring of invertebrates in terrestrial protected areas’, Koedoe 53(2), 137–149. https://doi.org/10.4102/koedoe.v53i2.1000 Roux, D., De Moor, F., Cambray, J. & Barber-James, H., 2002, ‘Use of landscape-level river signatures in conservation planning: A South African case study’, Conservation Ecology 6(2), 6, viewed October 2016, from http://www.consecol.org/vol6/iss2/art6. Sommer, S., Weibel, D., Blaser, N., Furrer, A., Wenzler, N.E., Rossler, W. et al., 2013, ‘Group recruitment in a thermophilic desert ant, Ocymyrmex robustior’, Journal of Comparative Physiology A – Neuroethology Sensory Neural and Behavioral Physiology 199(8), 711–722. https://doi.org/10.1007/s00359-013-0830-x South African National Parks (SANParks), 2016, Park management plan for the period 2016–2026, viewed October 2016, from https://www.sanparks.org/assets/docs/conservation/park_man/mznp-plan.pdf. Spellerberg, I.F. & Fedor, P.J., 2003, ‘A tribute to Claude Shannon (1916–2001) and a plea for more rigorous use of species richness, species diversity and the “Shannon–Wiener” Index’, Global Ecology and Biogeography 12(3), 177–179. https://doi.org/10.1046/j.1466-822X.2003.00015.x Van der Walt, P.T., 1980, ‘A phytosociological reconnaissance of the Mountain Zebra National Park’, Koedoe 23(1), 1–32. https://doi.org/10.4102/koedoe.v23i1.632 Vasconcelos, H.L., 1999, ‘Effects of forest disturbance on the structure of ground-foraging ant communities in central Amazonia’, Biodiversity & Conservation 8(3), 407–418. https://doi.org/10.1023/A:1008891710230