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the vegetation types and veld condition - Maremani Nature Reserve

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Prepared by:<br />

Ekotrust CC<br />

THE VEGETATION TYPES AND VELD CONDITION<br />

Dr Noel van Rooyen<br />

272 Thatchers Fields<br />

Lynnwood 0081<br />

Tel/Fax (012) 348 9043<br />

Cell 082 7077541<br />

E-mail: gvrooyen@icon.co.za<br />

of<br />

<strong>Maremani</strong><br />

August 2002


CONTENTS<br />

EXECUTIVE SUMMARY .............................................................................................................................. 1<br />

TERMS OF REFERENCE ............................................................................................................................ 3<br />

CHAPTER 1: INTRODUCTION .................................................................................................................... 4<br />

CHAPTER 2: THE STUDY AREA................................................................................................................. 6<br />

CHAPTER 3: METHODS.............................................................................................................................. 9<br />

CHAPTER 4: VEGETATION....................................................................................................................... 11<br />

CHAPTER 5: VEGETATION STRUCTURE ............................................................................................... 34<br />

CHAPTER 6: VELD CONDITION AND GRAZING CAPACITY.................................................................. 36<br />

CHAPTER 7: GAME ................................................................................................................................... 47<br />

CHAPTER 8: MANAGEMENT .................................................................................................................... 48<br />

CHAPTER 9: MONITORING....................................................................................................................... 52<br />

ACKNOWLEDGEMENTS ........................................................................................................................... 55<br />

REFERENCES............................................................................................................................................ 56<br />

APPENDIX A: PLANT SPECIES LIST........................................................................................................ 58


EXECUTIVE SUMMARY<br />

The aim of this project was to classify, describe <strong>and</strong> map <strong>the</strong> <strong>vegetation</strong> <strong>types</strong>, assess <strong>the</strong> <strong>veld</strong> <strong>condition</strong><br />

<strong>and</strong> determine <strong>the</strong> economic carrying capacity for grazer <strong>and</strong> browser wildlife of <strong>Maremani</strong>.<br />

<strong>Maremani</strong> is situated in <strong>the</strong> Limpopo Province, east of Messina, between approximately 22Ε 18' <strong>and</strong> 22Ε<br />

32' South, <strong>and</strong> 30Ε 13' <strong>and</strong> 30Ε 25' East. The reserve covers approximately 36583 ha. The area is<br />

characterised by plains, undulating <strong>and</strong> gravelly hills, rocky outcrops, higher mountain ranges, <strong>and</strong> rivers<br />

<strong>and</strong> streams. The altitude varies from approximately 427 m along <strong>the</strong> Limpopo River to 833 m at Mount<br />

Ga-Dowe on <strong>the</strong> farm Palm Grove.<br />

The mean annual rainfall for <strong>the</strong> <strong>Maremani</strong> area varies from 331 mm at Messina in <strong>the</strong> west to342 mm at<br />

Tshipise in <strong>the</strong> south. The rainy season is predominantly from October to March with about 85% of <strong>the</strong><br />

mean annual rainfall occurring during <strong>the</strong>se months. The driest months are from June to August. The<br />

mean annual temperature measured at Messina is 23.4ΕC while <strong>the</strong> extreme maximum <strong>and</strong> minimum<br />

temperatures measured at Messina are 43.8ΕC <strong>and</strong> 2.7ΕC respectively. The area is regarded as frost<br />

free.<br />

Stereo aerial photographs were used to stratify <strong>the</strong> area into relatively homogeneous units on <strong>the</strong> basis of<br />

physiography <strong>and</strong> <strong>vegetation</strong> cover, at a scale of 1: 50 000. The <strong>vegetation</strong> survey consisted of recording<br />

all identifiable plant species <strong>and</strong> allocating a percentage cover value to each species. The density<br />

(individuals per ha) of <strong>the</strong> tree <strong>and</strong> shrub layers was determined by counting individuals in a number of<br />

quadrats. A point survey of <strong>the</strong> grass layer was made to determine <strong>the</strong> frequency of grass species to<br />

calculate <strong>veld</strong> <strong>condition</strong> <strong>and</strong> <strong>the</strong> economic carrying capacity. The disc pasture meter was used to<br />

determine <strong>the</strong> amount of grass biomass.<br />

A classification of <strong>vegetation</strong> data was done with <strong>the</strong> TURBOVEG <strong>and</strong> MEGATAB computer programmes.<br />

Seventeen plant communities were distinguished on <strong>Maremani</strong> <strong>and</strong> <strong>the</strong> description of <strong>the</strong> plant<br />

communities is accompanied by a <strong>vegetation</strong> map at a scale of 1: 50 000. The percentage canopy cover,<br />

density <strong>and</strong> height of <strong>the</strong> different growth forms were used to determine <strong>the</strong> structure of each plant<br />

community.<br />

The <strong>veld</strong> <strong>condition</strong> <strong>and</strong> economic carrying capacity of <strong>the</strong> plant communities were assessed <strong>and</strong> <strong>the</strong><br />

present economic carrying capacity for <strong>the</strong> entire area is calculated as 39.2 ha/LAU. O<strong>the</strong>r methods were<br />

also used to determine <strong>the</strong> carrying capacity of <strong>the</strong> area, i.e. <strong>the</strong> Veld <strong>condition</strong>/rainfall method (40.7<br />

ha/LAU); Phytomass method (48 ha/LAU); Rainfall method (25.7 ha/LAU); <strong>the</strong> LAU/BU method<br />

(Snyman)(36.8 ha/LAU for grazers <strong>and</strong> 9.2 BU/100 ha (browsers). The recommended carrying capacity<br />

according to <strong>the</strong> LAU/BU method is 41.4 ha/LAU for grazers <strong>and</strong> 8 BU/100 ha(browsers).<br />

1


The present low grass biomass <strong>and</strong> poor species composition indicate <strong>veld</strong> that is not suitable for high<br />

numbers of high-selective grazer species.<br />

Game species that historically occurred in <strong>the</strong> area are Black Rhinoceros, Blue Wildebeest, Bushbuck,<br />

Bushpig, Buffalo, Duiker, El<strong>and</strong>, Giraffe, Grey Rhebuck, Hippopotamus, Impala, Klipspringer, Kudu,<br />

Ostrich, Reedbuck, Steenbok, Roan antelope, Sable antelope, Tsessebe, Warthog, Waterbuck, White<br />

Rhinoceros <strong>and</strong> Zebra. Species occurring on <strong>Maremani</strong> that were not historically from that area include<br />

Blesbok, Gemsbok <strong>and</strong> Red Hartebeest. Provision is made for 9% low-selective or bulk feeders (grazers),<br />

13% high selective grazers, 38% mixed grazers/browsers <strong>and</strong> 40% browsers. The low percentage of<br />

grazers is due to <strong>the</strong> poor <strong>condition</strong> of <strong>the</strong> grass layer <strong>and</strong> at this stage <strong>the</strong> area is more suitable for<br />

mixed feeders <strong>and</strong> browsers.<br />

Monitoring is an important aspect of <strong>veld</strong> management. Aspects that should be monitored routinely are<br />

rainfall, game numbers, game mortalities, game distribution, herd composition <strong>and</strong> birth rates. O<strong>the</strong>r<br />

aspects that are necessary to monitor include <strong>the</strong> <strong>veld</strong> <strong>condition</strong> in terms of plant species composition,<br />

species frequency, density <strong>and</strong>/or cover; carrying capacity; <strong>the</strong> effects of water provision on <strong>veld</strong> <strong>condition</strong><br />

<strong>and</strong> animal movements; <strong>the</strong> effects of bush encroachment; bush control; <strong>veld</strong> reclamation measures such<br />

as soil erosion control; <strong>and</strong> <strong>the</strong> effects of browsing on indicator plant species e.g. Baobab (Adansonia<br />

digitata), Shepherd’s tree (Boscia albitrunca), Common star chestnut (Sterculia rogersii), Sesame bush<br />

(Sesamothamnus lugardii), Marula (Sclerocarya birrea) <strong>and</strong> Corkwood species (Commiphora species).<br />

Approximately 71 tree species, 92 shrub species, 76 grass species, 7 sedge species, 9 geophytes, 30<br />

succulents, 6 parasites, 2 palm species, 2 fern species, 290 forb species <strong>and</strong> 14 alien species are listed,<br />

representing a total of 599 plant species.<br />

2


The assignment is interpreted as follows:<br />

TERMS OF REFERENCE<br />

Classify, describe <strong>and</strong> map <strong>the</strong> <strong>vegetation</strong> <strong>types</strong>, assess <strong>the</strong> <strong>veld</strong> <strong>condition</strong> <strong>and</strong> determine <strong>the</strong> ecological<br />

capacity of suitable grazer <strong>and</strong> browser game species for <strong>the</strong> area.<br />

1. Initial preparation<br />

Obtain all relevant maps (topocadastral, geology, l<strong>and</strong> <strong>types</strong>), stereo aerial photographs, climatic data<br />

(rainfall <strong>and</strong> temperature), as well as information on <strong>the</strong> infrastructure <strong>and</strong> natural environment of <strong>the</strong> area<br />

concerned. Stratification of <strong>the</strong> area into relatively homogeneous units on aerial photographs, by using a<br />

stereoscope, on <strong>the</strong> basis of physiography <strong>and</strong> <strong>vegetation</strong> cover.<br />

1. Vegetation <strong>and</strong> habitat survey<br />

Survey <strong>the</strong> stratified units <strong>and</strong> record all identifiable plant species, as well as habitat features, e.g.<br />

geology, topography, aspect, slope <strong>and</strong> rock cover. Classify <strong>the</strong> data by means of <strong>the</strong> TURBOVEG <strong>and</strong><br />

MEGATAB computer programs <strong>and</strong> describe <strong>and</strong> map <strong>the</strong> different plant communities. Identify alien<br />

species <strong>and</strong> possible encroacher/invasive plant species.<br />

Determine <strong>the</strong> structure of <strong>the</strong> plant communities in terms of canopy cover <strong>and</strong> density for different strata.<br />

Quantitatively survey <strong>the</strong> grass species composition to assess <strong>veld</strong> <strong>condition</strong> to calculate <strong>the</strong> economic<br />

carrying capacity of each plant community. Determine <strong>the</strong> aboveground grass biomass was determined.<br />

Identify <strong>and</strong> map management units based on <strong>vegetation</strong> <strong>types</strong>, environmental features, rivers <strong>and</strong> <strong>the</strong><br />

present road network. Compile a checklist of <strong>the</strong> plant species of <strong>the</strong> area.<br />

2. Economic carrying capacity for game<br />

Determine <strong>the</strong> grazing <strong>and</strong> browsing capacity for <strong>the</strong> area under long-term average rainfall <strong>condition</strong>s.<br />

Calculate <strong>the</strong> stocking rate based on present game numbers. Recommend game numbers <strong>and</strong> ratios of<br />

grazers <strong>and</strong> browsers for <strong>the</strong> area, based on present <strong>veld</strong> <strong>condition</strong> <strong>and</strong> economic capacity.<br />

Identify ecologically sensitive areas <strong>and</strong>/or problem areas in need of special management, e.g. bush<br />

encroached, eroded <strong>and</strong> degraded areas.<br />

3. Monitoring <strong>and</strong> recommodations<br />

Recommend aspects of <strong>the</strong> <strong>vegetation</strong> that should be managed <strong>and</strong> monitored.<br />

3


CHAPTER 2<br />

INTRODUCTION<br />

During <strong>the</strong> last decade or two, wildlife management has developed into a complicated <strong>and</strong> sophisticated,<br />

scientifically based enterprise. In practice <strong>the</strong> management of <strong>the</strong>se enterprises is often not based on<br />

ecological principles, resulting in <strong>the</strong> deterioration of <strong>the</strong> environment, <strong>and</strong> consequently in <strong>the</strong> loss of<br />

valuable natural assets <strong>and</strong> also <strong>the</strong> loss of <strong>the</strong> potential productivity of <strong>the</strong> <strong>veld</strong>. This does not only have<br />

economic consequences, but from a conservation viewpoint, <strong>the</strong> biological diversity of <strong>the</strong> natural<br />

ecosystem is influenced. To enable <strong>the</strong> assessment of <strong>veld</strong> <strong>condition</strong> <strong>and</strong> economic carrying capacity, an<br />

ecological evaluation of <strong>the</strong> area is necessary.<br />

Vegetation is probably <strong>the</strong> single-most influential characteristic of <strong>the</strong> environment that can reveal many<br />

pieces of vital information on various aspects of an area under observation. Not only is <strong>vegetation</strong> a large<br />

contributor when assessing environments in terms of mineral wealth <strong>and</strong> current health status, it is one of<br />

<strong>the</strong> largest role players when it comes to rectifying <strong>and</strong> rehabilitating lost <strong>and</strong> damaged habitats.<br />

Plant communities <strong>and</strong> <strong>the</strong>ir associated habitats form <strong>the</strong> basis of scientifically based environmental <strong>and</strong><br />

<strong>veld</strong> management plans. Each plant community has a certain characteristic plant species composition,<br />

that is mainly a result of <strong>the</strong> specific environmental composition of its habitat (climate, geology, rock<br />

cover, topography, soil <strong>types</strong>, drainage, water regime, etc.). The habitat also influences <strong>the</strong> distribution<br />

<strong>and</strong> structure of plant communities. However, plant communities may also be affected by <strong>the</strong> utilization<br />

history of <strong>the</strong> area. The specific potential of each plant community, with regard to habitat type for animals,<br />

grazing <strong>and</strong> browsing capacity <strong>and</strong> resilience to utilization <strong>and</strong> drought, is a direct result of <strong>the</strong> combined<br />

influence of environmental factors <strong>and</strong> past management. Consequently each plant community will react<br />

differently to certain <strong>vegetation</strong> management practices, for example grazing pressure, fire <strong>and</strong> utilization<br />

by man. Certain plant communities will show signs of deterioration sooner, under a particular<br />

management regime. The soils of certain plant communities are also more susceptible to erosion.<br />

All components of <strong>the</strong> <strong>Maremani</strong> ecosystems (physical environment, <strong>vegetation</strong>, animals) are interrelated<br />

<strong>and</strong> interdependent. A holistic approach is <strong>the</strong>refore imperative to conserve <strong>and</strong> utilize <strong>the</strong> given natural<br />

resources effectively. Ideally <strong>the</strong> area should be managed to be self-sustaining, while <strong>the</strong> quality <strong>and</strong><br />

diversity of <strong>the</strong> resources should not be allowed to decrease, as this would inevitably lead to ecosystem<br />

degradation <strong>and</strong> lower productivity.<br />

The objectives of a <strong>vegetation</strong> survey <strong>and</strong> <strong>veld</strong> management plan for <strong>Maremani</strong> are <strong>the</strong>refore to:<br />

5


! identify, describe <strong>and</strong> map <strong>the</strong> different plant communities;<br />

! contribute to <strong>the</strong> conservation of <strong>the</strong> habitats (ecosystems) of <strong>the</strong> area;<br />

! assess <strong>veld</strong> <strong>condition</strong> <strong>and</strong> economic carrying capacity;<br />

! stock <strong>the</strong> area with suitable game according to its economic carrying capacity;<br />

! increase <strong>the</strong> value of <strong>the</strong> l<strong>and</strong>; <strong>and</strong><br />

! contribute to <strong>the</strong> sustainable utilization of <strong>the</strong> area.<br />

6


Location<br />

CHAPTER 2<br />

STUDY AREA<br />

<strong>Maremani</strong> is situated in <strong>the</strong> Limpopo Province, east of Messina, between approximately 22Ε 18' <strong>and</strong> 22Ε<br />

32' South, <strong>and</strong> 30Ε 13' <strong>and</strong> 30Ε 25' East. The study area covers approximately 36583 ha.<br />

Terrain morphology<br />

The terrain morphology of <strong>the</strong> area is described by Kruger (1983) as very irregular plains <strong>and</strong> low hills<br />

with a relief from 30 m to 210 m, while more than 80% of <strong>the</strong> slopes has a slope of less than 5%. The<br />

area is characterised by plains, undulating <strong>and</strong> rocky hills, rocky outcrops, higher mountain ranges, rivers<br />

<strong>and</strong> seasonal streams. The altitude varies from approximately 427 m along <strong>the</strong> Limpopo River to 833 m at<br />

Mount Ga-Dowe on <strong>the</strong> farm Palm Grove. The altitude on <strong>the</strong> sou<strong>the</strong>rn border of <strong>the</strong> farm Solitude is<br />

about 488 m (Topocadastral maps at scale of 1: 50 000: 2230AA & AC Messina; 2230AD Esmefour;<br />

2230 Ga<strong>and</strong>rik; Government Printer, Pretoria).<br />

Geology<br />

Broadly <strong>the</strong> geology (lithology) of <strong>the</strong> study area from north-west to south-east includes:<br />

! gneiss <strong>and</strong> quartzite with gabbro in between;<br />

! calc-silicate rocks <strong>and</strong> gneiss;<br />

! basalt;<br />

! s<strong>and</strong>stone;<br />

! siltstone;<br />

! shale <strong>and</strong> mudstone;<br />

! dolerite; <strong>and</strong><br />

! s<strong>and</strong>stone <strong>and</strong> grit.<br />

Alluvium is found along <strong>the</strong> rivers <strong>and</strong> streams (see 2230 Messina, 1: 250 000 Geological Series map,<br />

Government Printer, Pretoria).<br />

7


L<strong>and</strong> Types <strong>and</strong> soils<br />

Nine l<strong>and</strong> <strong>types</strong> have been described <strong>and</strong> mapped for <strong>the</strong> area. These are: L<strong>and</strong> <strong>types</strong> Ib314, Ah88,<br />

Ah89, Ah91, Fc482, Fc483, Fc484, Ae265 <strong>and</strong> Ae266.<br />

The Ib314 l<strong>and</strong> type is described as ‘rocky areas with miscellaneous soils’ <strong>and</strong> covers part of <strong>the</strong> hilly<br />

areas in <strong>the</strong> north. Soils are derived from gneiss <strong>and</strong> quartzite.<br />

The Ah88 l<strong>and</strong> type has reddish s<strong>and</strong>y clay loam soils derived from dolerite, with a high clay content. The<br />

Ah89 l<strong>and</strong> type is characterised by reddish loamy s<strong>and</strong> to s<strong>and</strong>y loam derived from gneiss, <strong>and</strong> <strong>the</strong> Ah91<br />

l<strong>and</strong> type has red <strong>and</strong> yellow loamy s<strong>and</strong> derived from shale, mudstone <strong>and</strong> siltstone, with a clay content<br />

of less than 15%.<br />

In <strong>the</strong> Fc l<strong>and</strong> <strong>types</strong> calcrete <strong>and</strong> calcareous soils are present. The Fc482 l<strong>and</strong> type is characterised by<br />

loamy s<strong>and</strong> derived from s<strong>and</strong>stone, calc-silicate <strong>and</strong> quartzite, <strong>the</strong> Fc483 l<strong>and</strong> type has s<strong>and</strong>y loam soils<br />

derived from gneiss, <strong>and</strong> <strong>the</strong> Fc484 l<strong>and</strong> type has loam s<strong>and</strong>y soils derived from gneiss <strong>and</strong> quartzite.<br />

The Ae265 l<strong>and</strong> type consists of reddish s<strong>and</strong>y loam to s<strong>and</strong>y clay loam soils derived from basalt. The<br />

soils are usually deeper than 300 mm. Within <strong>the</strong> Ae266 l<strong>and</strong> type reddish s<strong>and</strong>y loam soils, derived<br />

from gneiss, are found.<br />

Soils derived from gneiss, quartzite <strong>and</strong> s<strong>and</strong>stone are usually leached <strong>and</strong> have a low nutrient content<br />

whereas soils derived from shale, siltstone, mudstone, dolerite <strong>and</strong> basalt are usually more clayey <strong>and</strong><br />

have a higher nutrient content <strong>and</strong> water-holding capacity.<br />

Silty <strong>and</strong> clayey alluvial soils occur on flood plains along <strong>the</strong> Limpopo <strong>and</strong> Njelele Rivers as well as along<br />

streams <strong>and</strong> in <strong>the</strong> wetl<strong>and</strong> of <strong>the</strong> Mutanga River in <strong>the</strong> south of <strong>the</strong> farm Solitude.<br />

Climate<br />

The mean annual rainfall for <strong>the</strong> <strong>Maremani</strong> area varies from 331 mm at Messina in <strong>the</strong> west to 342 mm at<br />

Tshipise in <strong>the</strong> south (Tables 1 & 2; Erasmus 1987; Wea<strong>the</strong>r Bureau 1988). The rainy season is<br />

predominantly from October to March, with approximately 85% of <strong>the</strong> mean annual rainfall occurring<br />

during <strong>the</strong>se months. The driest months are from June to August (Table 1 <strong>and</strong> Figure 1). The maximum<br />

rainfall measured in 24 hours was 167 mm (Table 3). Evaporation is much higher than <strong>the</strong> annual rainfall.<br />

8


Rainfall is <strong>the</strong> primary driving force influencing productivity of <strong>the</strong> <strong>vegetation</strong>, <strong>the</strong>refore <strong>the</strong> economic<br />

carrying capacity for <strong>the</strong> area was calculated at a mean annual rainfall of 340 mm. After prolonged<br />

drought <strong>the</strong> area can become totally unsuitable for animal production (especially for grazers) <strong>and</strong><br />

appropriate measures should be taken to avoid animal losses, e.g. reducing animal numbers <strong>and</strong><br />

supplementary feeding.<br />

The mean annual temperature for <strong>the</strong> region is 23.4ΕC (Table 4). The mean daily maximum for<br />

December is 32.3ΕC <strong>and</strong> for July 26.6ΕC. The mean daily minimum for December is 21.1ΕC <strong>and</strong> for June<br />

10.6ΕC. The extreme maximum <strong>and</strong> minimum temperature measured at Messina over a period of 43<br />

years were 43.8ΕC <strong>and</strong> 2.7ΕC respectively (Table 4). The area is regarded as frost free.<br />

The mean percentage relative humidity for <strong>the</strong> area is given in Table 5.<br />

9


Approach<br />

CHAPTER 3<br />

METHODS<br />

Stereo aerial photographs were provided by <strong>the</strong> client. For proper <strong>and</strong> efficient surveying, an ecological<br />

stratification of 1: 50 000 scale aerial photographs on <strong>the</strong> basis of terrain morphology <strong>and</strong> <strong>vegetation</strong><br />

cover should be made beforeh<strong>and</strong>. This stratification is used to determine <strong>the</strong> position <strong>and</strong> number of<br />

sample plots, <strong>and</strong> is <strong>the</strong> basis for identifying habitat <strong>types</strong>.<br />

Vegetation surveys<br />

An assessment of <strong>the</strong> habitat, e.g. dominant plant species, topography, geology, rocky outcrops <strong>and</strong> rock<br />

cover, soil texture, soil depth, slope <strong>and</strong> aspect, <strong>and</strong> a visual assessment of <strong>veld</strong> <strong>condition</strong> were made at<br />

each sampling plot.<br />

The <strong>vegetation</strong> survey consisted of recording all identifiable trees, shrubs, grasses, sedges, ferns, forbs,<br />

geophytes, succulents, palms <strong>and</strong> alien (exotic) plants within each sample plot. Forbs are herbaceous<br />

plants not considered as grasses. Each species was allocated a percentage cover value which is required<br />

for <strong>the</strong> classification <strong>and</strong> description of <strong>the</strong> plant communities.<br />

An estimate of <strong>the</strong> total <strong>vegetation</strong> cover (%) was given for different strata: trees above 6 m, from 3 m to 6<br />

m, shrubs below 3 m, as well as <strong>the</strong> herbaceous layer (grasses <strong>and</strong> forbs). The density (individuals per<br />

ha) of <strong>the</strong> tree <strong>and</strong> shrub layers was determined by counting individuals in several quadrats. The average<br />

height of <strong>the</strong> different strata was estimated as well as <strong>the</strong> maximum height of <strong>the</strong> large trees.<br />

Where possible, a point survey of <strong>the</strong> grass layer was made to determine <strong>the</strong> frequency (%) of grass<br />

species which is an indication of <strong>the</strong> dominance or importance of <strong>the</strong> species. The information was used<br />

to calculate <strong>veld</strong> <strong>condition</strong> <strong>and</strong> <strong>the</strong> economic carrying capacity of each plant community.<br />

The disc pasture meter was used, where possible, to determine <strong>the</strong> amount of grass biomass (fuel load).<br />

The rocky outcrops were excluded from measurements with <strong>the</strong> disc pasture meter.<br />

10


Data analyses<br />

A classification of <strong>the</strong> <strong>vegetation</strong> data was done with <strong>the</strong> TURBOVEG <strong>and</strong> MEGATAB computer<br />

programmes (see Table 6). The description of plant communities includes <strong>the</strong> high tree, tree, shrub,<br />

grass <strong>and</strong> forb (herbaceous) layers. The plant species recorded for <strong>the</strong> quarter degree grids that include<br />

<strong>Maremani</strong> were obtained from <strong>the</strong> PRECIS data bank of <strong>the</strong> National Herbarium at <strong>the</strong> National Botanical<br />

Institute, Pretoria. All species recorded in <strong>the</strong> sample plots are listed in Table 6 <strong>and</strong> in Appendix A. The<br />

description of <strong>the</strong> plant communities is accompanied by a <strong>vegetation</strong> map at a scale of 1: 50 000 (Figure<br />

2).<br />

Vegetation structure in terms of canopy cover, density <strong>and</strong> height of <strong>the</strong> woody species are given in<br />

Tables 7, 8 & 9 <strong>and</strong> Figures 3 to 7. The phytomass production of <strong>the</strong> different <strong>vegetation</strong> <strong>types</strong> is given in<br />

Table 10.<br />

The subdivision of <strong>the</strong> area into larger units (zones or management units) is based on floristically related<br />

<strong>vegetation</strong> <strong>types</strong>, but geology, topography, existing roads <strong>and</strong> rivers were also taken into account to<br />

produce relatively homogeneous <strong>and</strong> practical units (Figure 8).<br />

The economic carrying capacity of each <strong>vegetation</strong> unit was determined with <strong>the</strong> Ecological Index<br />

Method. This incorporates <strong>the</strong> classification of species into ecological groups. These groups e.g.<br />

Decreasers <strong>and</strong> Increasers 1, 2a, 2b <strong>and</strong> 2c, are based on <strong>the</strong> reaction of <strong>the</strong> species to grazing<br />

pressure, its palatability, biomass production <strong>and</strong> preference by herbivores.<br />

O<strong>the</strong>r methods to determine <strong>the</strong> economic carrying capacity for wildlife on game ranches were used <strong>and</strong><br />

<strong>the</strong> values obtained compared with <strong>the</strong> Ecological Index method e.g. <strong>the</strong> Combined <strong>veld</strong> <strong>condition</strong> <strong>and</strong><br />

rainfall method (Danckwerts 1989); <strong>the</strong> Herbaceous Phytomass method (Moore & Odendaal 1987); <strong>the</strong><br />

Rainfall method (Coe, Cumming & Philllipson 1976); <strong>and</strong> <strong>the</strong> Graze/ Browse Unit method (Snyman 1991;<br />

Dekker 1996; 1997).<br />

The economic carrying capacity, game numbers obtained from recent (2001) counts, <strong>and</strong> recommended<br />

numbers of species are given in Tables 12 to 15. Game that historically occurred in <strong>the</strong> area, are listed<br />

(see Chapter 10) <strong>and</strong> <strong>the</strong> ratio of suitable species in terms of low <strong>and</strong> high selective grazers, mixed<br />

feeders <strong>and</strong> browsers, are given in Tables 12 & 15.<br />

11


CHAPTER 4<br />

VEGETATION<br />

The area was described <strong>and</strong> mapped by Acocks (1988) as Mopane Veld (<strong>veld</strong> dominated by<br />

Colophospermum mopane), while Low & Rebelo (1998) classified <strong>the</strong> area as Mopane Bush<strong>veld</strong>.<br />

According to <strong>the</strong>ir estimate about 38% of <strong>the</strong> Mopane Bush<strong>veld</strong> is conserved, mainly in <strong>the</strong> nor<strong>the</strong>rn<br />

Kruger National Park (Low & Rebelo 1998).<br />

Differences in topography, geology, rockiness, drainage, soil texture <strong>and</strong> depth, slope, <strong>the</strong> presence of<br />

calcrete <strong>and</strong> previous l<strong>and</strong>-use have resulted in differences in <strong>vegetation</strong>. Each <strong>vegetation</strong> unit <strong>the</strong>refore<br />

represents a different ecosystem, with its own set of habitat <strong>condition</strong>s <strong>and</strong> plant species composition.<br />

The area is arid <strong>and</strong> relies on rainfall events for fodder production to sustain <strong>the</strong> animals. Supplementary<br />

feeding is sometimes needed to prevent severe loss of <strong>condition</strong> or mortalities among animals.<br />

Seventeen plant communities were distinguished on <strong>Maremani</strong> (Table 6) <strong>and</strong> mapped as such<br />

(Figure 2).<br />

These 17 plant communities on <strong>Maremani</strong> can be grouped into six main <strong>vegetation</strong> <strong>types</strong>:<br />

A. Rocky outcrops with <strong>the</strong> Small-leaved rock fig (Ficus tettensis), Large-leaved rock fig<br />

(Ficus abutilifolia), Paperbark corkwood (Commiphora marlothii) <strong>and</strong> Mountain grass<br />

(Danthoniopsis dinteri) <strong>the</strong> conspicuous species (communities 1, 2 <strong>and</strong> 3);<br />

B. Mopane <strong>veld</strong> on gneiss <strong>and</strong> quartzite dominated by Mopane (Colophospermum<br />

mopane), Low<strong>veld</strong> cluster-leaf (Terminalia prunioides), White syringa (Kirkia<br />

acuminata), Red bushwillow (Combretum apiculatum), Resin gardenia (Gardenia<br />

resiniflua,) <strong>and</strong> Mountain grass (Danthoniopsis dinteri)(communities 4, 5, 6, 7 & 8).<br />

This broad <strong>vegetation</strong> type is fur<strong>the</strong>r divided into two sub<strong>types</strong> based on environmental<br />

features:<br />

! Mopane bush<strong>veld</strong> on undulating low rocky hills <strong>and</strong> gravelly slopes on<br />

12


shallow soils derived from gneiss <strong>and</strong> quartzite (community 4, Table 6), with Mopane<br />

(Colophospermum mopane), Red bushwillow (Combretum apiculatum), Jacket-plum<br />

(Pappea capensis), Stunted plane (Ochna inermis), White-stem corkwood<br />

(Commiphora tenuipetiolata), Xerophyta viscosa <strong>and</strong> Mountain grass<br />

(Danthoniopsis dinteri) <strong>the</strong> diagnostic species.<br />

! Mopane woodl<strong>and</strong> on plains with moderately deep, to deep soils derived<br />

from gneiss <strong>and</strong> quartzite, <strong>and</strong> a low rock cover (communities 5, 6, 7 & 8, Table 6). Tall<br />

trees of Mopane (Colophospermum mopane), White syringa (Kirkia acuminata) <strong>and</strong><br />

Marula (Sclerocarya birrea) are prominent. O<strong>the</strong>r abundant trees include Red<br />

bushwillow (Combretum apiculatum), Velvet corkwood (Commiphora mollis),<br />

Common star chestnut (Sterculia rogersii), Blue-thorn (Acacia erubescens), Silver<br />

raisin (Grewia monticola) <strong>and</strong> False marula (Lannea schweinfurthii).<br />

C. Low Mopane bush<strong>veld</strong> <strong>and</strong> thickets on calcrete, shale <strong>and</strong> basalt dominated by<br />

Mopane (Colophospermum mopane), Stink shepherd’s tree (Boscia foetida), Mopane<br />

pomegranate (Rhigozum zambesiacum), Trumpet thorn (Catophractes alex<strong>and</strong>ri),<br />

Transvaal sesame bush (Sesamothamnus lugardii), Narrow-leaved mustard tree<br />

(Salvadora australis), <strong>the</strong> grasses Tetrapogon tenellus <strong>and</strong> Thimble grass<br />

(Fingerhuthia africana) <strong>and</strong> <strong>the</strong> forb Monechma divaricatum (communities 9, 10 <strong>and</strong><br />

11).<br />

D. Species-poor Mopane thickets <strong>and</strong> forests in lowl<strong>and</strong>s <strong>and</strong> along watercourses, where<br />

Mopane (Colophospermum mopane), Low<strong>veld</strong> cluster-leaf (Terminalia prunioides)<br />

<strong>and</strong> Shepherd’s tree (Boscia albitrunca) are <strong>the</strong> dominant species (communities 11, 12<br />

<strong>and</strong> 13).<br />

E. Disturbed areas (overgrazed <strong>veld</strong>, old fields, watering points <strong>and</strong> kraals) where Umbrella<br />

thorn (Acacia tortilis) <strong>and</strong> Sickle bush (Dichrostachys cinerea) are <strong>the</strong> dominant<br />

species (community 14); <strong>and</strong><br />

F. Riverine communities on alluvial floodplains, with Leadwood (Combretum imberbe),<br />

Apple-leaf (Philenoptera violacea), Nyala tree (Xanthocercis zambesiaca), Ilala palm<br />

(Hyphaene coriacea) <strong>and</strong> Cyperus sexangularis <strong>the</strong> dominant species (communities 15,<br />

16 <strong>and</strong> 17) (Table 6 <strong>and</strong> Figure 2).<br />

The following plant communities were distinguished:<br />

13


1. Croton gratissimus - Danthoniopsis dinteri rocky outcrops<br />

(Lavender feverberry - Mountain grass rocky outcrops)<br />

1.1 Ent<strong>and</strong>rophragma caudatum - Portulacaria afra mountain bush<strong>veld</strong><br />

(Mountain mahogany - Porkbush mountain bush<strong>veld</strong>)<br />

2. Androstachys johnsonii - Terminalia sericea s<strong>and</strong>stone hills<br />

(Lebombo iron wood - Silver cluster-leaf s<strong>and</strong>stone hills)<br />

3. Combretum apiculatum - Danthoniopsis dinteri - Tricholaena monachne rocky outcrops<br />

(Red bushwillow - Mountain grass - Blue-seed grass rocky outcrops)<br />

4. Colophospermum mopane - Xerophyta viscosa open to dense bush<strong>veld</strong> on low hills <strong>and</strong> rocky<br />

outcrops<br />

(Mopane - Xerophyta viscosa open to dense bush<strong>veld</strong> <strong>and</strong> low hills <strong>and</strong> rocky outcrops)<br />

5. Colophospermum mopane - Terminalia prunioides - Psiadia punctulata bush<strong>veld</strong><br />

(Mopane - Low<strong>veld</strong> cluster-leaf - Psiadia bush<strong>veld</strong><br />

6. Sclerocarya birrea - Aristida stipitata - Eragrostis lehmanniana open grass <strong>and</strong> bush<strong>veld</strong><br />

(Marula - Long-awned three-awn - Lehmann’s love grass open grass <strong>and</strong> bush<strong>veld</strong>)<br />

7. Colophospermum mopane - Kirkia acuminata - Acacia erubescens plains bush<strong>veld</strong> <strong>and</strong> woodl<strong>and</strong><br />

(Mopane - White syringa - Blue thorn plains bush<strong>veld</strong> <strong>and</strong> woodl<strong>and</strong>)<br />

8. Colophospermum mopane - Boscia albitrunca - Terminalia prunioides open to dense bush<strong>veld</strong> on<br />

plains <strong>and</strong> low rocky hills<br />

(Mopane - Shepherd’s tree - Low<strong>veld</strong> cluster-leaf open to dense bush<strong>veld</strong> on plains <strong>and</strong> low rocky<br />

hills)<br />

9. Colophospermum mopane - Catophractes alex<strong>and</strong>ri - Vernonia cinarescens low <strong>and</strong> dense<br />

bush<strong>veld</strong><br />

(Mopane - Trumpet thorn - Vernonia low <strong>and</strong> dense bush<strong>veld</strong>)<br />

10. Colophospermum mopane - Sesamothamnus lugardii - Acacia tortilis open to dense low bush<strong>veld</strong><br />

(Mopane - Transvaal sesame bush - Umbrella thorn open to dense low bush<strong>veld</strong>)<br />

11. Colophospermum mopane - Gardenia resiniflua - Tetrapogon tenellus low thicket<br />

(Mopane - Resin gardenia - Tetrapogon low thicket)<br />

12. Colophospermum mopane - Aristida adscensionis bush<strong>veld</strong><br />

(Mopane - Nine-awned grass bush<strong>veld</strong><br />

13. Colophospermum mopane - Acacia tortilis - Eragrostis lehmanniana low dense bush<strong>veld</strong><br />

(Mopane - Umbrella thorn - Lehmann’s love grass low dense bush<strong>veld</strong>)<br />

14. Acacia tortilis - Eragrostis lehmanniana old fields<br />

(Umbrella thorn - Lehmann’s love grass old fields)<br />

14


15. Pechuel-loeschia leubnitziae - Urochloa mosambicensis open grassl<strong>and</strong> to dense bush<strong>veld</strong><br />

(Wild sage - Common signal grass open grassl<strong>and</strong> to dense bush<strong>veld</strong>)<br />

16. Combretum imberbe - Philenoptera violacea stream community<br />

(Leadwood - Apple-leaf stream community)<br />

17. Xanthocercis zambeziaca - Acacia robusta - Cyperus sexangularis riparian community<br />

(Nyala tree - Brack thorn - Cyperus riparian community)<br />

Description of <strong>the</strong> plant communities:<br />

1. Croton gratissimus - Danthoniopsis dinteri rocky outcrops<br />

(Lavender feverberry - Mountain grass rocky outcrops)<br />

This community occurs scattered on s<strong>and</strong>stone, dolerite <strong>and</strong> gneiss rocky outcrops in <strong>the</strong><br />

Steenbokr<strong>and</strong>jes <strong>and</strong> Palm Grove area <strong>and</strong> in <strong>the</strong> east <strong>and</strong> south on Frampton, Skirbeek, Dawn, Solitude<br />

<strong>and</strong> Bosbokpoort, <strong>and</strong> covers approximately 936 ha (Figure 2). It occurs on shallow red to brown s<strong>and</strong>y<br />

loam soils with a rock cover of 60% to 100%.<br />

The diagnostic species are <strong>the</strong> Lavender feverberry (Croton gratissimus), Cork bush (Mundulea sericea)<br />

<strong>and</strong> Natal guarri (Euclea natalensis) (species group 1, Table 6).<br />

High trees (>6 m) have an average canopy cover of 2% <strong>and</strong> are characterised by <strong>the</strong> Shepherd’s tree<br />

(Boscia albitrunca), Paperbark corkwood (Commiphora marlothii), White syringa (Kirkia acuminata),<br />

Mountain False-thorn (Albizia brevifolia) <strong>and</strong> Small-leaved rock fig (Ficus tettensis).<br />

Trees cover on average 5% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are <strong>the</strong> Lavender fever-berry (Croton<br />

gratissimus), Red bushwillow (Combretum apiculatum), Large-leaved rock fig (Ficus abutilifolia),<br />

Sjambokpod (Cassia abbreviata) <strong>and</strong> <strong>the</strong> Low<strong>veld</strong> milkberry (Manilkara mochisia).<br />

Shrubs cover on average 20% of <strong>the</strong> area <strong>and</strong> are characterised by <strong>the</strong> Corkbush (Mundulea sericea),<br />

Natal guarri (Euclea natatensis), <strong>and</strong> Knobbly creeper (Combretum mossambicense).<br />

The grass layer covers on average 40% of <strong>the</strong> area. Grass species such as Mountain grass<br />

(Danthoniopsis dinteri), Finger grass (Digitaria eriantha), S<strong>and</strong> quick (Schmidtia pappophoroides), <strong>and</strong><br />

Blue-seed grass (Tricholaena monachne) are locally abundant.<br />

15


Herbaceous species in this community cover 5% of <strong>the</strong> area, with Barleria affinis a prominent perennial<br />

species.<br />

1.1 Ent<strong>and</strong>rophragma caudatum - Portulacaria afra mountain bush<strong>veld</strong><br />

(Mountain mahogany - Porkbush mountain bush<strong>veld</strong>)<br />

This community occurs on gneiss <strong>and</strong> quartzitic mountains in <strong>the</strong> north of <strong>Maremani</strong>. The <strong>vegetation</strong> on<br />

<strong>the</strong>se high mountains of Palm Grove <strong>and</strong> Malalahoek e.g. Ga-Dowe, differ floristically from <strong>the</strong> o<strong>the</strong>r hills<br />

<strong>and</strong> rocky outcrops on <strong>Maremani</strong> due to <strong>the</strong> presence of diagnostic species such as Mountain mahogany<br />

(Ent<strong>and</strong>rophragma caudatum), Porkbush (Portulacaria afra), Wild apricot (Ancylobotrys capensis) <strong>and</strong><br />

Aloe globuligemma. This community covers approximately 381 ha.<br />

2. Androstachys johnsonii - Terminalia sericea s<strong>and</strong>stone hills<br />

(Lebombo iron wood - Silver cluster-leaf s<strong>and</strong>stone hills)<br />

This community occurs mainly on <strong>the</strong> rocky s<strong>and</strong>stone ridge in <strong>the</strong> south-eastern parts of <strong>Maremani</strong> <strong>and</strong><br />

covers approximately 491 ha (Figure 2). It forms <strong>the</strong> sou<strong>the</strong>rn border of <strong>the</strong> farms Dawn, Frampton <strong>and</strong><br />

Skirbeek, <strong>and</strong> <strong>the</strong> nor<strong>the</strong>rn border of Solitude. It occurs on shallow to deep red-brown loamy s<strong>and</strong> with a<br />

rock cover varying from 50 to 100%.<br />

Some of <strong>the</strong> diagnostic species are <strong>the</strong> Lebombo iron wood (Androstachys johnsonii), Silver cluster-leaf<br />

(Terminalia sericea), Herringbone grass (Pogonarthria squarrosa), <strong>the</strong> grass Digitaria milanjiana <strong>and</strong> <strong>the</strong><br />

sedge Coleochloa pallidior (see species group 2, Table 6).<br />

High trees (>6 m) have an average canopy cover of 1% <strong>and</strong> are characterised by Mountain false-thorn<br />

(Albizia brevifolia), Propeller tree (Gyrocarpus americanus), Shepherd’s tree (Boscia albitrunca) <strong>and</strong> <strong>the</strong><br />

Low<strong>veld</strong> milk berry (Manilkara mochisia).<br />

Trees (>3 - 6 m) cover on average 13% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are <strong>the</strong> Lebombo iron wood<br />

(Androstachys johnsonii), Silver cluster-leaf (Terminalia sericea), Small-leaved rock fig (Ficus tettensis)<br />

<strong>and</strong> Paperbark corkwood (Commiphora marlothii).<br />

Shrub species (


pseudopulchellus), Shakama plum (Hexalobus monopetalus) <strong>and</strong> <strong>the</strong> Large-leaved rock fig (Ficus<br />

abutilifolia).<br />

The grass layer is well developed <strong>and</strong> covers on average 85% of <strong>the</strong> area. The dominant grass species<br />

<strong>and</strong> <strong>the</strong>ir percentage frequency are:<br />

Lehmann’s love grass (Eragrostis lehmanniana) 74%<br />

Herringbone grass (Pogonarthria squarrosa) 14%<br />

Guinea grass (Panicum maximum) 10%<br />

Annual three-awn (Aristida adscensionis) 2%<br />

O<strong>the</strong>r conspicuous grass species are Aristida transvaalensis, Danthoniopsis dinteri, Tricholaena<br />

monachne <strong>and</strong> Digitaria milanjiana.<br />

Herbaceous forb, fern <strong>and</strong> sedge species in this sub-community cover 5% of <strong>the</strong> area <strong>and</strong> include<br />

Tephrosia villosa, Coleochloa pallidior <strong>and</strong> Pellaea calomelanos.<br />

An interesting feature found in <strong>the</strong> Tshipise s<strong>and</strong>stone ridges to <strong>the</strong> south of Dawn, Frampton <strong>and</strong><br />

Skirbeek are <strong>the</strong> round or oval-shaped hollows on <strong>the</strong> rocky summits. These hollows are usually one to<br />

three metres in diameter <strong>and</strong> more or less 1 metre deep. They resemble potholes <strong>and</strong> were probably<br />

created by water <strong>and</strong> wind erosion. These ‘rock tanks’ or pools accumulate some soil at <strong>the</strong> bottom where<br />

plants become established. During <strong>the</strong> rainy season <strong>the</strong> hollows are filled with water <strong>and</strong> <strong>the</strong> plant<br />

species have to complete <strong>the</strong>ir life cycle before <strong>the</strong> pools dry up during winter. Some species are<br />

submerged, e.g. bladder wort (Utricularia stellaris) <strong>and</strong> ‘babergras’ (Lagarosiphon crispus); floating<br />

species are duck weed (Lemna species), rooted <strong>and</strong> floating species are <strong>the</strong> water lily (Nymphaea<br />

caerulea) <strong>and</strong> Aponogeton junceus; <strong>and</strong> in <strong>the</strong> moist soil on <strong>the</strong> edges, sedge species (Cyperus spp.) as<br />

well as water clover (Marsilea ephippiocarpa), Kyllinga alba <strong>and</strong> <strong>the</strong> grass Eragrostis tenella are found.<br />

When <strong>the</strong> hollows dry out <strong>the</strong>se plants survive as seed, spores or rhizomes until <strong>the</strong> next rainy season.<br />

3. Combretum apiculatum - Danthoniopsis dinteri - Tricholaena monachne rocky outcrops<br />

(Red bushwillow - Mountain grass - Blue-seed grass rocky outcrops)<br />

This community occurs widespread on mostly isolated gneiss <strong>and</strong> quartzite rocky outcrops <strong>and</strong> <strong>the</strong> crests<br />

of ridges (Figure 2). It covers approximately 763 ha (Figure 2) <strong>and</strong> occurs on shallow <strong>and</strong> gravelly red-<br />

brown loamy s<strong>and</strong> to s<strong>and</strong>y loam soils with a rock cover varying from 40% to 100%. Slopes vary from 8 to<br />

15°. The <strong>vegetation</strong> composition occurring on <strong>the</strong> white <strong>and</strong> black rocky outcrops is very similar.<br />

17


The diagnostic species are <strong>the</strong> Carrot tree (Steganotaenia araliaceae), Spear grass (Heteropogon<br />

contortus) <strong>and</strong> Abutilon pycnodon (species group 4, Table 6).<br />

High trees (>6 m) have an average canopy cover of 3% <strong>and</strong> are characterised by <strong>the</strong> Small-leaved rock<br />

fig (Ficus tettensis), Mopane (Colophospermum mopane), White syringa (Kirkia acuminata), Shepherd’s<br />

tree (Boscia albitrunca), Marula (Sclerocarya birrea) <strong>and</strong> Boabab (Adansonia digitata).<br />

Trees (>3 - 6 m) cover on average 14% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are <strong>the</strong> Large-leaved rock<br />

fig (Ficus abutilifolia), Red bushwillow (Combretum apiculatum), Mopane (Colophospermum mopane),<br />

Low<strong>veld</strong> cluster-leaf (Terminalia prunioides), Common star chestnut (Sterculia rogersii) <strong>and</strong> <strong>the</strong> Giant<br />

raisin (Grewia hexamita).<br />

Shrubs (


ocky outcrops<br />

(Mopane - Xerophyta viscosa open to dense bush<strong>veld</strong> <strong>and</strong> low hills <strong>and</strong> rocky outcrops)<br />

This community occurs on <strong>the</strong> rocky crests <strong>and</strong> slopes of <strong>the</strong> lower hills <strong>and</strong> ridges in <strong>the</strong> nor<strong>the</strong>rn part of<br />

<strong>Maremani</strong>, north-west of <strong>the</strong> Malaladrif road <strong>and</strong> covers approximately 1398 ha (Figure 2). The slopes<br />

vary from 5 to 20Ε. It occurs on a shallow <strong>and</strong> gravelly red to brown s<strong>and</strong>y loam soil derived from gneiss<br />

<strong>and</strong> quartzite with a rock cover varying from 20% against <strong>the</strong> lower slopes to 80% on <strong>the</strong> crests of <strong>the</strong> low<br />

hills.<br />

Locally <strong>the</strong> <strong>vegetation</strong> resembles a woodl<strong>and</strong> with high trees of White syringa (Kirkia acuminata) <strong>and</strong><br />

Marula (Sclerocarya birrea) <strong>the</strong> prominent species. Small knobwood (Zanthoxylum capense), Mountain<br />

grass (Danthoniopsis dinteri) <strong>and</strong> Blue-seed grass (Tricholaena monachne) are also conspicuous<br />

species.<br />

The diagnostic species are Jacket-plum (Pappea capensis), Xerophyta viscosa <strong>and</strong> Hippocratea<br />

africana (species group 6, Table 6).<br />

High trees (>6 m) have an average canopy cover of 6% <strong>and</strong> are characterised by White syringa (Kirkia<br />

acuminata), Mopane (Colophospermum mopane), Marula (Sclerocarya birrea), Shepherd’s tree (Boscia<br />

albitrunca) <strong>and</strong> Knobthorn (Acacia nigrescens).<br />

Trees (>3 m - 6 m) cover on average 10% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane), Red bushwillow (Combretum apiculatum), Low<strong>veld</strong> cluster-leaf (Terminalia<br />

prunioides) <strong>and</strong> White-stem corkwood (Commiphora tenuipetiolata).<br />

Shrubs (


Species such as Stink grass (Bothriochloa radicans) <strong>and</strong> Nine-awn grass (Enneapogon cenchroides)<br />

occur locally abundant.<br />

Forb species in this community cover 4% of <strong>the</strong> area <strong>and</strong> dense st<strong>and</strong>s of Tephrosia villosa occur locally.<br />

O<strong>the</strong>r forb species include Indigofera heterotricha, Justicia betonica <strong>and</strong> Ptycholobium contortum.<br />

5. Colophospermum mopane - Terminalia prunioides - Psiadia punctulata bush<strong>veld</strong><br />

(Mopane - Low<strong>veld</strong> cluster-leaf - Psiadia bush<strong>veld</strong><br />

This mopane bush<strong>veld</strong> occurs on <strong>the</strong> low hills of <strong>the</strong> farms Bosbokpoort, Dawn, Reitz <strong>and</strong> Senator in <strong>the</strong><br />

central parts of <strong>Maremani</strong>. The geological substrate consists mainly of gneiss, quartzite <strong>and</strong> basalt<br />

(Figure 2). This bush<strong>veld</strong> covers approximately 893 ha <strong>and</strong> occurs on shallow <strong>and</strong> gravelly greyish s<strong>and</strong>y<br />

loam soils with a rock cover varying from 10% to 70%. Slopes vary from 1 to 4°.<br />

The diagnostic species are Psiadia punctulata <strong>and</strong> Abutilon angulatum var. angulatum (species group 7,<br />

Table 6).<br />

High trees (>6 m) have an average canopy cover of 5% <strong>and</strong> are characterised by scattered individuals of<br />

White syringa (Kirkia acuminata), Knobthorn (Acacia nigrescens), Mopane (Colophospermum mopane),<br />

Tall common corkwood (Commiphora gl<strong>and</strong>ulosa), Slender three-hook thorn (Acacia senegal var.<br />

leiorhachis) <strong>and</strong> Shepherd’s tree (Boscia albitrunca).<br />

Trees >3 m - 6 m) cover on average 12% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane), Low<strong>veld</strong> cluster-leaf (Terminalia prunioides), Red bushwillow (Combretum<br />

apiculatum), Common star chestnut (Sterculia rogersii) <strong>and</strong> Velvet corkwood (Commiphora mollis)<br />

Shrubs (


S<strong>and</strong> quick (Schmidtia pappophoroides) 3%<br />

Blue buffalo grass (Cenchrus ciliaris) 2%<br />

Dwarf grass (Oropetium capense) 2%<br />

Species with a frequency of 2% <strong>and</strong> lower are listed in Table 6.<br />

Forb species in this community cover 6% of <strong>the</strong> area <strong>and</strong> include Tephrosia villosa, Abutilon austro-<br />

africanum <strong>and</strong> Ocimum americanum.<br />

6. Sclerocarya birrea - Aristida stipitata - Eragrostis lehmanniana open grass <strong>and</strong> bush<strong>veld</strong><br />

(Marula - Long-awned three-awn - Lehmann’s love grass open grass <strong>and</strong> bush<strong>veld</strong>)<br />

This open s<strong>and</strong><strong>veld</strong> covers approximately 1106 ha <strong>and</strong> occurs mainly on <strong>the</strong> plains <strong>and</strong> gentle foot slopes<br />

of <strong>the</strong> hills as well as old fields or previously cultivated areas on Frampton, Skirbeek <strong>and</strong> Dawn in <strong>the</strong><br />

south of <strong>Maremani</strong> (Figure 2). It occurs on deep red loamy s<strong>and</strong> derived from s<strong>and</strong>stone, calc-silicate<br />

<strong>and</strong> quartzite. The s<strong>and</strong>y soils are underlain by calcrete in places. Rocks are mostly absent in this<br />

community. Silver cluster-leaf (Terminalia sericea), S<strong>and</strong> quick (Schmidtia pappohoroides) <strong>and</strong> Silky<br />

bushman grass (Stipagrostis uniplumis) are some of <strong>the</strong> characteristic species.<br />

The diagnostic species are Long-awned three-awn (Aristida stipitata) <strong>and</strong> Wild medlar (Vangueria<br />

infausta) (Species group 8, Table 6).<br />

High trees (>6 m) have an average canopy cover of 3% <strong>and</strong> are characterised by scattered individuals of<br />

Marula (Sclerocarya birrea), Mopane (Colophospermum mopane) <strong>and</strong> Boabab (Adansonia digitata).<br />

Trees (>3 m - 6 m) cover on average 9% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane), Marula (Sclerocarya birrea), Silver cluster-leaf (Terminalia sericea),<br />

Umbrella thorn (Acacia tortilis) <strong>and</strong> Shepherd’s tree (Boscia albitrunca).<br />

Shrubs (


Lehmann’s love grass (Eragrostis lehmanniana) 55%<br />

Natal Redtop (Melinis repens) 8%<br />

Silky bushman grass (Stipagrostis uniplumis) 8%<br />

Annual three-awn (Aristida adscensionis) 7%<br />

S<strong>and</strong> quick (Schmidtia pappophoroides) 7%<br />

Guinea grass (Panicum maximum) 7%<br />

Long-awned three-awn (Aristida stipitata) 6%<br />

Species with a frequency of 6% or lower are listed in Table 6 <strong>and</strong> include Giant three-awn (Aristida<br />

meridionalis).<br />

Forb species in this community cover 5% of <strong>the</strong> area <strong>and</strong> include Abutilon austro-africanum, Ocimum<br />

americanum, Dicerocaryum eriocarpum <strong>and</strong> Ptycholobium contortum.<br />

7. Colophospermum mopane - Kirkia acuminata - Acacia erubescens plains bush<strong>veld</strong> <strong>and</strong><br />

woodl<strong>and</strong><br />

(Mopane - White syringa - Blue thorn plains bush<strong>veld</strong> <strong>and</strong> woodl<strong>and</strong>)<br />

Communities 7 <strong>and</strong> 8 are closely related, but <strong>the</strong> presence of species such as Blue thorn (Acacia<br />

erubescens), Zebra-bark corkwood (Commiphora viminea), Cissus cornifolia <strong>and</strong> Jatropha spicata<br />

differentiate between <strong>the</strong>se two communities. The <strong>veld</strong> of community 7 is also in very poor <strong>condition</strong> in<br />

comparison with community 8.<br />

This community is found north <strong>and</strong> west of <strong>the</strong> Njelele River, mainly on undulating low hills <strong>and</strong> plains<br />

(valleys)(Figure 2). This open woodl<strong>and</strong> is characterise by high trees of White syringa (Kirkia acuminata),<br />

Marula (Sclerocarya birrea) <strong>and</strong> Mopane (Colophospermum mopane), with Red bushwillow (Combretum<br />

apiculatum) one of <strong>the</strong> prominent lower trees. This community covers approximately 6630 ha (Figure 2)<br />

<strong>and</strong> occurs on shallow <strong>and</strong> gravelly red to brown loamy s<strong>and</strong> to s<strong>and</strong>y loam soils derived from gneiss <strong>and</strong><br />

quartzite, with a rock or gravel cover varying from 5 to 20%, <strong>and</strong> locally up to 80% where outcrops occur.<br />

The area is mostly flat <strong>and</strong> <strong>the</strong> gentle slopes vary from 1 to 5Ε.<br />

The diagnostic species consist of Blue thorn (Acacia erubescens), Cissus cornifolia <strong>and</strong> Jatropha<br />

spicata (species group 9, Table 6).<br />

22


High trees (>6 m) have an average canopy cover of 7% <strong>and</strong> are characterised by White syringa (Kirkia<br />

acuminata), Marula (Sclerocarya birrea), Mopane (Colophospermum mopane), Boabab (Adansonia<br />

digitata), Slender three-hook thorn (Acacia senegal var. leiorhachis) <strong>and</strong> Knobthorn (Acacia nigrescens).<br />

Trees (>3 m - 6 m) cover on average 15% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane), Red bushwillow (Combretum apiculatum), Zebra-bark corkwood<br />

(Commiphora viminea), Velvet corkwood (Commiphora mollis), Low<strong>veld</strong> cluster leaf (Terminalia<br />

prunioides), Tall common corkwood (Commiphora gl<strong>and</strong>ulosa) <strong>and</strong> Common star chestnut (Sterculia<br />

rogersii).<br />

Shrubs (


This <strong>vegetation</strong> type varies from a low <strong>and</strong> dense bush<strong>veld</strong> to an open woodl<strong>and</strong> in places. It occurs on<br />

<strong>the</strong> undulating plains <strong>and</strong> lowl<strong>and</strong>s (valleys) north <strong>and</strong> west of <strong>the</strong> Njelele River (Figure 2) <strong>and</strong> covers<br />

approximately 9813 ha (Figure 2). It occurs on shallow <strong>and</strong> gravelly to moderately deep red to brown<br />

s<strong>and</strong>y loam soils derived from gneiss <strong>and</strong> quartzite. The gravel <strong>and</strong> rock cover varying from 3 to 20% <strong>and</strong><br />

up to 40% in places. The slopes vary from 1 to 12Ε.<br />

Diagnostic species are absent, but <strong>the</strong> absence of species from species groups 6 to 9 (Table 6), <strong>and</strong> <strong>the</strong><br />

presence of species from species groups 10, 11 <strong>and</strong> 12 , characterise this community.<br />

High trees (>6 m) have an average canopy cover of 7% <strong>and</strong> are characterised by White syringa (Kirkia<br />

acuminata), Shepherd’s tree (Boscia albitrunca), Slender three-hook thorn (Acacia senegal var.<br />

leiorhachis), Mopane (Colophospermum mopane), Marula (Sclerocarya birrea), <strong>and</strong> Baobab (Adansonia<br />

digitata).<br />

Trees (>3 m - 6 m) cover on average 17% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Red bushwillow<br />

(Combretum apiculatum), Velvet corkwood (Commiphora mollis), Mopane (Colophospermum mopane),<br />

Tall common corkwood (Commiphora gl<strong>and</strong>ulosa), Green-stem corkwood (Commiphora neglecta),<br />

Common star chestnut (Sterculia rogersii), False marula (Lannea schweinfurthii) <strong>and</strong> Low<strong>veld</strong> cluster-leaf<br />

(Terminalia prunioides). The valleys have dense st<strong>and</strong>s of Colophospermum mopane, while Corkwoods<br />

(Commiphora species) form dense st<strong>and</strong>s locally.<br />

Shrubs (


Dwarf grass (Oropetium capense) 3%<br />

Flaccid finger grass (Digitaria velutina) 3%<br />

Blue-seed grass (Tricholaena monachne), S<strong>and</strong> Quick (Schmidtia pappophoroides) <strong>and</strong> Guinea grass<br />

(Panicum maximum), occur locally. O<strong>the</strong>r grass species with a frequency of less than 3% are listed in<br />

Table 6.<br />

Forb species cover 11% of <strong>the</strong> area <strong>and</strong> include Indigofera bainesii, Blepharis subvolubilis, Barleria<br />

prionitis, Abutilon austro-africanum, Tephrosia villosa <strong>and</strong> Ocimum americanum.<br />

9. Colophospermum mopane - Catophractes alex<strong>and</strong>ri - Vernonia cinarescens low <strong>and</strong> dense<br />

bush<strong>veld</strong><br />

(Mopane - Trumpet thorn - Vernonia low <strong>and</strong> dense bush<strong>veld</strong>)<br />

This community covers approximately 7000 ha (Figure 2) <strong>and</strong> can be found on <strong>the</strong> gabbro plains of<br />

Boschr<strong>and</strong>, Steenbokr<strong>and</strong>jes, Vryheid <strong>and</strong> Bok<strong>veld</strong> in <strong>the</strong> north-west, as well as on <strong>the</strong> basalt, calc-<br />

silcrete <strong>and</strong> gneiss of Woodhall, Skirbeek, Frampton <strong>and</strong> Njeleles Drift in <strong>the</strong> east of <strong>Maremani</strong>. It occurs<br />

on shallow <strong>and</strong> gravelly red to brown s<strong>and</strong>y loam calcareous soils <strong>and</strong> although rocks are absent in<br />

places, up to 30% of <strong>the</strong> area can be covered by rocks. The slopes vary from 0 to 2Ε. Calcrete is common<br />

in <strong>the</strong> soil horizon. Bush densification is clearly visible in this <strong>vegetation</strong> type as a result of an abundance<br />

of watering points <strong>and</strong> overgrazing in <strong>the</strong> past <strong>and</strong> <strong>the</strong> presence of ab<strong>and</strong>oned old fields.<br />

The presence of Stink shepherd’s tree (Boscia foetida), Trumpet thorn (Catophractes alex<strong>and</strong>ri) <strong>and</strong><br />

Mopane pomegranate (Rhigozum zambesiacum) shows <strong>the</strong> relationship between communities 9, 10 <strong>and</strong><br />

11 (species group 17, Table 6).<br />

The diagnostic species are Trumpet thorn (Catophractes alex<strong>and</strong>ri), Gymnosporia pubescens <strong>and</strong><br />

Vernonia cinarescens (species group 13, Table 6).<br />

High trees (>6 m) have an average canopy cover of 1% <strong>and</strong> are characterised by Mopane<br />

(Colophospermum mopane), Tall common corkwood (Commiphora gl<strong>and</strong>ulosa), Slender three-hook thorn<br />

(Acacia senegal var. leiorhachis) <strong>and</strong> Shepherd’s tree (Boscia albitrunca).<br />

Trees (>3 m - 6 m) cover on average 19% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane), Low<strong>veld</strong> cluster-leaf (Terminalia prunioides), Common star chestnut<br />

(Sterculia rogersii), White-stem corkwood (Commiphora tenuipetiolata) <strong>and</strong> Velvet corkwood<br />

25


(Commiphora mollis).<br />

Shrubs (


There are also open grassy patches dominated by Pan dropseed (Sporobolus ioclados), dense patches<br />

of high Mopane forest as well as dense low scrub Mopane, especially along <strong>the</strong> drainage lines.<br />

The diagnostic species are Transvaal sesame bush (Sesamothamnus lugardii), Three-hook thorn<br />

(Acacia senegal var. rostrata), Horned thorn (Acacia gr<strong>and</strong>icornuta), Small green thorn (Balanites<br />

pedicellaris) <strong>and</strong> <strong>the</strong> Kalahari s<strong>and</strong> raisin (Grewia retinervis) (species group 14, Table 6).<br />

High trees (>6 m) have an average canopy cover of 3% <strong>and</strong> are characterised by Mopane<br />

(Colophospermum mopane).<br />

Trees (>3 m - 6 m ) cover on average 14% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Umbrella thorn<br />

(Acacia tortilis), Mopane (Colophospermum mopane), Horned thorn (Acacia gr<strong>and</strong>icornuta), Low<strong>veld</strong><br />

cluster leaf (Terminalia prunioides), Tall common corkwood (Commiphora gl<strong>and</strong>ulosa) <strong>and</strong> Shepherd’s<br />

tree (Boscia albitrunca).<br />

Shrubs (


Forb species in this community cover 9% of <strong>the</strong> area <strong>and</strong> include Blepharis diversispina, Abutilon austro-<br />

africanum <strong>and</strong> Ocimum americanum.<br />

11. Colophospermum mopane - Gardenia resiniflua - Tetrapogon tenellus thicket<br />

(Mopane - Resin gardenia - Tetrapogon thicket)<br />

This thicket community occurs in <strong>the</strong> south on <strong>the</strong> plains of <strong>the</strong> farms Woodhall, Frampton <strong>and</strong> Dawn <strong>and</strong><br />

<strong>the</strong> irregular terrain of Solitude <strong>and</strong> covers approximately 418 ha (Figure 2). It occurs on moderately deep<br />

red s<strong>and</strong>s on calcrete as well as shallow yellow to red s<strong>and</strong>y clay loam derived from shale, mudstone <strong>and</strong><br />

siltstone. The s<strong>and</strong>y soils are underlain by calcrete in some places. The rock cover varies from 3 to 20%<br />

<strong>and</strong> locally up to 80%. The slopes are less than 4Ε.<br />

Thimble grass (Fingerhuthia africana) is a poor diagnostic species for community 11 (species group 15,<br />

Table 6), but o<strong>the</strong>r characteristic species are Tetrapogon tenellus <strong>and</strong> Resin gardenia (Gardenia<br />

resiniflua).<br />

High trees (>6 m) have an average canopy cover of less than 1% <strong>and</strong> are characterised by Mopane<br />

(Colophospermum mopane) <strong>and</strong> <strong>the</strong> Shepherd’s tree (Boscia albitrunca).<br />

Trees (>3 m - 6 m) cover on average 19% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane) <strong>and</strong> <strong>the</strong> Shepherd’s tree (Boscia albitrunca).<br />

Shrubs (


Tetrapogon tenellus 5%<br />

Species with a frequency of 5% or lower include Nine-awned grass (Enneapogon cenchroides), Flaccid<br />

finger grass (Digitaria velutina), Sweet signal grass (Brachiaria erusiformis), Natal Redtop (Melinis<br />

repens), False signal grass (Brachiaria deflexa) <strong>and</strong> Blue buffalo grass (Cenchrus ciliaris). Thimble grass<br />

(Fingerhuthia africana) <strong>and</strong> Tetrapogon tenellus are conspicuous on <strong>the</strong> hilly <strong>and</strong> gravelly areas.<br />

Forb species in this community cover 3% of <strong>the</strong> area <strong>and</strong> include Abutilon austro-africanum.<br />

12. Colophospermum mopane - Aristida adscensionis bush<strong>veld</strong><br />

(Mopane - Nine-awned grass bush<strong>veld</strong><br />

This plant community occurs scattered over <strong>Maremani</strong> (Vryheid, Palm Grove, Njelele’s Drift, Woodhall,<br />

Lenin) on <strong>the</strong> lowl<strong>and</strong>s, plains <strong>and</strong> lower slopes of <strong>the</strong> hills <strong>and</strong> covers approximately 2041 ha (Figure 2).<br />

It occurs on a shallow to deep red s<strong>and</strong>y loam derived from s<strong>and</strong>stone, gneiss <strong>and</strong> gabbro. The rock<br />

cover varies from 0 to 30% <strong>and</strong> <strong>the</strong> slopes are less than 4Ε. Forests of Mopane are found locally in <strong>the</strong><br />

valleys in <strong>the</strong> west.<br />

A diagnostic species group is absent but species such as Stunted plane (Ochna inermis), Mallow raisin<br />

(Grewia villosa), Melhania rehmannii <strong>and</strong> Zebra-bark corkwood (Commiphora viminea) are characteristic<br />

species (species groups 18 & 19, Table 6).<br />

High trees (>6 m) have an average canopy cover of 8% <strong>and</strong> are characterised by Mopane<br />

(Colophospermum mopane), Shepherd’s tree (Boscia albitrunca) <strong>and</strong> White syringa (Kirkia acuminata).<br />

Trees (>3 m - 6 m) cover on average 19% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane), Shepherd’s tree (Boscia albitrunca), Zebra-bark corkwood (Commiphora<br />

viminea), Low<strong>veld</strong> cluster-leaf (Terminalia prunioides) <strong>and</strong> Slender three-hook thorn (Acacia senegal var.<br />

leiorhachis).<br />

Shrubs (


Lehmann’s love grass (Eragrostis lehmanniana) 14%<br />

Dwarf grass (Oropetium capense) 9%<br />

False signal grass (Brachiaria deflexa) 4%<br />

Silky bushman grass (Stipagrostis uniplumis) 4%<br />

Natal Redtop (Melinis repens) 4%<br />

Carrot seed grass (Tragus berteronianus) 3%<br />

Forb species in this community cover 6% of <strong>the</strong> area <strong>and</strong> include Abutilon austro-africanum <strong>and</strong> Barleria<br />

prionitis.<br />

13. Colophospermum mopane - Eragrostis lehmanniana low dense bush<strong>veld</strong><br />

(Mopane - Lehmann’s love grass low dense bush<strong>veld</strong>)<br />

This species poor thicket to open bush<strong>veld</strong> occurs mainly on <strong>the</strong> plains of Senator <strong>and</strong> Lenin but is also<br />

found locally in Riverview, Reitz, Njelele’s Drift <strong>and</strong> Dawn (Figure 2). It is dominated by Mopane<br />

(Colophospermum mopane), <strong>and</strong> Low<strong>veld</strong> cluster-leaf (Terminalia prunioides). It covers approximately<br />

1738 ha. This community occurs on shallow to deep grey to red s<strong>and</strong>y loam soils derived from gneiss <strong>and</strong><br />

quartzite. The rock cover varies from 1 to 10% <strong>and</strong> locally up to 50%. The slopes are less than 2Ε.<br />

A diagnostic species group is absent but species such as Mopane (Colophospermum mopane), Low<strong>veld</strong><br />

cluster leaf (Terminalia prunioides) <strong>and</strong> <strong>the</strong> Shepherd’s tree (Boscia albitrunca) are abundant species<br />

(species groups 20 & 21, Table 6). This community is <strong>the</strong>refore also characterised by <strong>the</strong> absence of<br />

diagnostic species from species groups 1 to 19 (Table 6).<br />

High trees (>6 m) have an average canopy cover of 3% <strong>and</strong> are characterised by <strong>the</strong> Mopane<br />

(Colophospermum mopane), Shepherd’s tree (Boscia albitrunca), Marula (Sclerocarya birrea) <strong>and</strong><br />

Boabab (Adansonia digitata).<br />

Trees (>3 m - 6 m) cover on average 11% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Mopane<br />

(Colophospermum mopane), Low<strong>veld</strong> cluster-leaf (Terminalia prunioides), Velvet corkwood (Commiphora<br />

mollis), Common star chestnut (Sterculia rogersii), Red bushwillow (Combretum apiculatum) <strong>and</strong> Tall<br />

common corkwood (Commiphora gl<strong>and</strong>ulosa).<br />

Shrubs (


The grass layer is in poor <strong>condition</strong> <strong>and</strong> covers on average 15% of <strong>the</strong> area. The dominant grass species<br />

<strong>and</strong> <strong>the</strong>ir percentage frequency are:<br />

Annual three-awn (Aristida adscensionis) 25%<br />

Lehmann’s love grass (Eragrostis lehmanniana) 24%<br />

Silky bushman grass (Stipagrostis uniplumis) 7%<br />

Spreading three-awn (Aristida congesta subsp. barbicollis) 6%<br />

False signal grass (Brachiaria deflexa) 6%<br />

S<strong>and</strong> quick (Schmidtia pappophoroides) 2%<br />

Forb species in this community cover 4% of <strong>the</strong> area <strong>and</strong> include Abutilon austro-africanum, Ocimum<br />

americanum <strong>and</strong> Indigofera bainesii.<br />

14. Acacia tortilis - Eragrostis lehmanniana old fields<br />

(Umbrella thorn - Lehmann’s love grass old fields)<br />

These disturbed areas (overgrazed <strong>veld</strong>, old fields, watering points <strong>and</strong> kraals) occur scattered over <strong>the</strong><br />

plains of <strong>Maremani</strong> (Figure 2). This community covers approximately 460 ha <strong>and</strong> occurs on deep red<br />

s<strong>and</strong>y loam soils derived from gneiss, s<strong>and</strong>stone <strong>and</strong> basalt, as well as on alluvial soils along <strong>the</strong><br />

seasonal streams. Rocks are absent.<br />

A diagnostic species group is absent but species such as Umbrella thorn (Acacia tortilis), Sickle bush<br />

(Dichrostachys cinerea), Mopane (Colophospermum mopane), Lehmann’s love grass (Eragrostis<br />

lehmanniana) <strong>and</strong> Annual three-awn (Aristida adscensionis) are prominent (species groups 22 & 23,<br />

Table 6). This community is <strong>the</strong>refore also characterised by <strong>the</strong> absence of species from species group<br />

20 & 21, for example Low<strong>veld</strong> cluster-leaf (Terminalia prunioides), Red bushwillow (Combretum<br />

apiculatum), Slender three-hook thorn (Acacia senegal var. leiorhachis), Tall common corkwood<br />

(Commiphora gl<strong>and</strong>ulosa), White syringa (Kirkia acuminata), Common star chestnut (Sterculia rogersii)<br />

<strong>and</strong> Blue sourplum (Ximenia americana).<br />

High trees (>6 m) cover less than 1% <strong>and</strong> are characterised by Mopane (Colophospermum mopane) <strong>and</strong><br />

Marula (Sclerocarya birrea).<br />

Trees (>3 m - 6 m) cover on average 5% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species is Umbrella thorn (Acacia<br />

tortilis), Mopane (Colophospermum mopane), Shepherd’s tree (Boscia albitrunca) <strong>and</strong> Knobthorn (Acacia<br />

nigrescens).<br />

31


Shrubs (


Trees (>3 m - 6 m) cover on average 5% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are <strong>the</strong> Umbrella thorn<br />

(Acacia tortilis).<br />

Shrubs (


The diagnostic species are for example Leadwood (Combretum imberbe), Buffalo thorn (Ziziphus<br />

mucronata), Ilala palm (Hyphaene coriacea), Sporobolus consimilis <strong>and</strong> Weeping boer-bean (Schotia<br />

brachypetala) (species group 26, Table 6). Species such as Cyperus sexangularis, Apple-leaf<br />

(Philenoptera violacea), Red spike-thorn (Gymnosporia senegalensis) <strong>and</strong> Nyala tree (Xanthocercis<br />

zambeziaca) are also prominent species in this community (species group 28, Table 6). Community 16 is<br />

related to community 17 through <strong>the</strong> presence of species from species group 28 (Table 6).<br />

High trees (>6 m) have an average canopy cover of 10% <strong>and</strong> are characterised by Leadwood<br />

(Combretum imberbe), Weeping boer-bean (Schotia brachypetala) <strong>and</strong> Knobthorn (Acacia nigrescens).<br />

Trees (>3 m - 6 m) cover on average 8% of <strong>the</strong> area <strong>and</strong> <strong>the</strong> dominant species are Umbrella thorn<br />

(Acacia tortilis) <strong>and</strong> Buffalo thorn (Ziziphus mucronata).<br />

Shrubs (


prominent species in this community (species group 25, Table 6) as well as Cyperus sexangularis, Apple-<br />

leaf (Philenoptera violacea), Red spike-thorn (Gymnosporia senegalensis), Nyala tree (Xanthocercis<br />

zambeziaca), Leadwood (Combretum imberbe) (species group 28, Table 6).<br />

High trees (>6 m) include <strong>the</strong> Common cluster fig (Ficus sycomorus), Nyala tree (Xanthocercis<br />

zambeziaca), Brack thorn (Acacia robusta subsp. clavigera), Leadwood (Combretum imberbe), Apple-leaf<br />

(Philenoptera violacea), Large-leaved false thorn (Albizia versicolor), Ana tree (Faidherbia albida), <strong>and</strong><br />

Fever tree (Acacia xanthophloea).<br />

The dominant tree species are Flame thorn (Acacia ataxacantha), Apple-leaf (Philenoptera violacea),<br />

Knobthorn (Acacia nigrescens), Umbrella thorn (Acacia tortilis), Buffalo thorn (Ziziphus mucronata),<br />

Brown ivory (Berchemia discolor), Jackal berry (Diospyros mespiliformis), Large feverberry (Croton<br />

megalobotrys) <strong>and</strong> Flame creeper (Combretum paniculatum).<br />

Shrubs cover on average 9% of <strong>the</strong> area <strong>and</strong> are characterised by Red spike-thorn (Gymnosporia<br />

senegalensis), Large feverberry (Croton megalobotrys), Savanna gardenia (Gardenia volkensii), Magic<br />

guarri (Euclea divinorum), Wild sage (Pechuel-loeschia leubnitziae), Bulrush (Typha capensis), <strong>and</strong><br />

Woolly caper bush (Capparis tomentosa).<br />

The grass layer is well developed <strong>and</strong> covers on average 49% of <strong>the</strong> area. The dominant sedge species<br />

is Cyperus sexangularis while grass species are represented by <strong>the</strong> Common reed (Phragmites australis),<br />

Broad-leaved panicum (Panicum deustum), Guinea grass (Panicum maximum), Common signal grass<br />

(Urochloa mosambicensis), Swamp grass (Diplachne fusca), Blue buffalo grass (Cenchrus ciliaris) <strong>and</strong><br />

Pearly love grass (Eragrostis rotifer). Herbaceous <strong>and</strong> weedy species in this community cover 10% of <strong>the</strong><br />

area <strong>and</strong> include Abutilon angulatum, Pluchea dioscoridis, Xanthium strumarium, Ageratum conyzoides,<br />

Schoenoplectus corymbosus <strong>and</strong> Datura stramonium.<br />

35


Introduction<br />

CHAPTER 5<br />

VEGETATION STRUCTURE<br />

The primary elements of <strong>vegetation</strong> structure are growth form, stratification <strong>and</strong> cover. Vertical structure is<br />

a function of different growth forms (or size classes) dominating certain layers <strong>and</strong> can be expressed in<br />

terms of canopy cover <strong>and</strong>/or density of each growth form. Density also indicates <strong>the</strong> spatial distribution of<br />

different growth forms, populations or individual species. Vegetation can be classified according to<br />

structure without reference to species names, <strong>and</strong> layer or size class diagrams can be used to illustrate<br />

structure by using for example cover or density of each layer.<br />

Size classes are considered to be good indicators of browse quality <strong>and</strong> quantity. Although a plant<br />

community is defined to have a relatively homogeneous floristic composition, structure <strong>and</strong> habitat,<br />

different floristic communities can have <strong>the</strong> same structure or vice versa. Structure can also relate to <strong>the</strong><br />

feeding pattern of animals as well as <strong>the</strong> suitability of a habitat for different animal species. The available<br />

leaf mass <strong>and</strong> volume at different height levels are valuable in determining <strong>the</strong> suitability of a habitat for<br />

browser species.<br />

Density of <strong>the</strong> woody species can affect <strong>the</strong> <strong>condition</strong> of <strong>the</strong> herbaceous layer. Several studies have<br />

indicated that <strong>the</strong> grass production declines when <strong>the</strong> tree <strong>and</strong> shrub density exceeds 1500 individuals<br />

per hectare.<br />

Cover<br />

The mean percentage canopy cover <strong>and</strong> <strong>the</strong> variation within <strong>the</strong> communities for different strata <strong>and</strong><br />

<strong>vegetation</strong> <strong>types</strong> are summarised in Table 7 <strong>and</strong> Figures 3 & 4. The percentage cover of <strong>the</strong> high tree<br />

stratum is <strong>the</strong> lowest in communities 1, 2, 9, 11, 14 <strong>and</strong> 15, representing <strong>the</strong> communities on rocks,<br />

calcareous soils <strong>and</strong> disturbed areas (old fields)(Figure 3). Tree cover was higher tha 15% in communities<br />

7, 8, 9, 11 <strong>and</strong> 12, while communities with a dense shrub layer are communities 2, 10, 11 <strong>and</strong> 12. The<br />

highest grass cover was found in <strong>the</strong> south-east on <strong>the</strong> footslopes of <strong>the</strong> gneiss <strong>and</strong> s<strong>and</strong>stone hills<br />

(community 6), as well as in <strong>the</strong> old fields along <strong>the</strong> major rivers <strong>and</strong> <strong>the</strong> riverine communities<br />

(communities 15, 16 <strong>and</strong> 17)(Figure 4). Forbs were abundant in areas where calcrete occurs, for example<br />

community 9. It is apparent that <strong>the</strong> communities with <strong>the</strong> lowest shrub <strong>and</strong> rock cover were associated<br />

with a high grass cover (communities 6, 15, 16 <strong>and</strong> 17).<br />

36


Density<br />

The mean densities of <strong>the</strong> different height classes <strong>and</strong> <strong>the</strong> variation within <strong>the</strong> communities are<br />

summarised in Figures 5, 6 <strong>and</strong> 7 <strong>and</strong> Table 8. Community 4 has <strong>the</strong> most tall trees, with community 9<br />

<strong>and</strong> 11 <strong>the</strong> most trees per ha (Table 8 <strong>and</strong> Figures 5, 6 <strong>and</strong> 7). The highest mean shrub density of all <strong>the</strong><br />

communities was found in communities 11, 12 <strong>and</strong> 13 where up to 2400 individuals per hectare occurred<br />

in places. This seems to be above <strong>the</strong> threshold where <strong>the</strong> <strong>vegetation</strong> density has an effect on grass<br />

production.<br />

Tree height<br />

The mean height of <strong>the</strong> woody strata, as well as <strong>the</strong> maximum height of <strong>the</strong> high tree stratum are<br />

summarised in Table 9.<br />

37


Introduction<br />

CHAPTER 6<br />

VELD CONDITION AND ECONOMIC CARRYING CAPACITY<br />

<strong>Maremani</strong> is representative of <strong>the</strong> Mopane Bush<strong>veld</strong> <strong>and</strong> <strong>the</strong> grazing can be considered as sweet <strong>veld</strong>.<br />

Veld <strong>condition</strong> as well as <strong>the</strong> carrying capacity of <strong>the</strong> area in general, will vary from season to season,<br />

depending mainly on <strong>the</strong> rainfall, <strong>and</strong> also to a certain extent on past <strong>and</strong> present utilization. Each of <strong>the</strong><br />

recognised plant communities is associated with a specific habitat, has its own diagnostic species<br />

composition, <strong>and</strong> <strong>the</strong>refore also has its own grazing <strong>and</strong> browsing potential <strong>and</strong> economic <strong>and</strong> ecological<br />

carrying capacity.<br />

The concepts of economic <strong>and</strong> ecological carrying capacities need to be explained. Game numbers<br />

will increase from an initial low to a level where <strong>the</strong> available food, water <strong>and</strong> shelter resources become<br />

limiting (Caughley 1977). Numbers increase slowly at first <strong>and</strong> once a critical stage is reached, <strong>the</strong> growth<br />

rate is exponential <strong>and</strong> numbers increase rapidly. At a certain upper level, density-dependent factors such<br />

as competition for resources, lower fecundity <strong>and</strong> increased mortalities result in a leveling-off of population<br />

growth to a point where births equal deaths, <strong>and</strong> net growth (or yield) is zero. In practice, <strong>the</strong> ultimate<br />

population density fluctuates around a fluctuating upper level, which arises from, for example, variations in<br />

rainfall, inter-specific competition, predator-prey relations or accidental fires. The level around which <strong>the</strong><br />

population oscillates is known as <strong>the</strong> ecological carrying capacity. It is <strong>the</strong> population level that is likely<br />

to exist in unmanaged large natural areas. Fluctuations in numbers can be quite dramatic, with severe<br />

crashes occurring during periods of prolonged drought or disease epidemics. Allowing certain species to<br />

attain high densities may impact negatively on o<strong>the</strong>r more sensitive species. Therefore, should <strong>the</strong><br />

management objective be to increase species diversity, <strong>the</strong> numbers of aggressively competitive species<br />

need to be controlled.<br />

If a population is maintained below <strong>the</strong> ecological carrying capacity by cropping, <strong>the</strong> net growth of <strong>the</strong><br />

population is positive, as <strong>the</strong>re is room for expansion in <strong>the</strong> form of resource abundance. The population<br />

is <strong>the</strong>n at an economic carrying capacity. There is no one single economic carrying capacity but <strong>the</strong>re is<br />

a point at which maximum sustained yield (MSY) is obtained, usually around 70 to 80% of <strong>the</strong> ecological<br />

carrying capacity.<br />

Different equations have been proposed to calculate carrying capacity of an area. In general, by<br />

combining an ecological or <strong>veld</strong> <strong>condition</strong> index, <strong>the</strong> grass production <strong>and</strong>/or canopy cover, rainfall, <strong>the</strong><br />

incidence of fire, accessibility of <strong>the</strong> terrain, grazing habits <strong>and</strong> social behaviour of animal species, it is<br />

39


possible to estimate an economic capacity for a particular plant community or game ranch. The ecological<br />

capacity is usually conservatively estimated to be 20% to 30% higher than <strong>the</strong> economic capacity.<br />

Methods<br />

The following approach is based on <strong>the</strong> Ecological Index Method (Vorster 1982), but was adapted for <strong>the</strong><br />

specific area.<br />

The grass species found in <strong>the</strong> different plant communities were arranged according to <strong>the</strong>ir percentage<br />

frequencies within <strong>the</strong> communities. This indicates of <strong>the</strong> degree of dominance <strong>and</strong> <strong>the</strong> distribution of <strong>the</strong><br />

relevant species. The grass species were also classified into categories that are based on <strong>the</strong>ir reaction to<br />

grazing, palatability <strong>and</strong> production potential (see Appendix A - grasses).<br />

The categories are:-<br />

D = Decreaser - <strong>the</strong>se species are abundant in <strong>veld</strong> in a good <strong>condition</strong> <strong>and</strong> decrease when <strong>the</strong> <strong>veld</strong> is<br />

over- or under-utilized (valuable grass species)<br />

I1 = Increaser 1 - <strong>the</strong>se species increase in <strong>veld</strong> that is under-utilized.<br />

I2a = Increaser 2a - <strong>the</strong>se species increase in <strong>veld</strong> that is lightly <strong>and</strong>/or selectively over-utilized.<br />

I2b = Increaser 2b - <strong>the</strong>se species increase in <strong>veld</strong> that is moderately <strong>and</strong>/or selectively over-utilized.<br />

I2c = Increaser 2c - <strong>the</strong>se species increase in <strong>veld</strong> that is severely over-utilized (weeds <strong>and</strong><br />

encroacher species.<br />

Bare areas were recorded when <strong>the</strong>re was no grass species within a metre from <strong>the</strong> step point.<br />

By using <strong>the</strong>se categories, an ecological index is calculated to express <strong>veld</strong> <strong>condition</strong>. Theoretically, <strong>the</strong><br />

maximum ecological index value that can be obtained, is 100 %, i.e. if all species present are classified as<br />

Decreasers. Veld in a good <strong>condition</strong>, with a high grazing capacity, has a high percentage Decreaser <strong>and</strong><br />

Increaser 1 grass species. By using <strong>the</strong> ecological index, <strong>the</strong> total grass canopy cover, <strong>the</strong> percentage<br />

canopy cover of trees <strong>and</strong> shrubs, annual rainfall, fire regime <strong>and</strong> accessibility of <strong>the</strong> area, an economic<br />

capacity is calculated for each plant community. The economic capacity of <strong>Maremani</strong> was calculated for<br />

game at a mean annual rainfall of 340 mm. The availability of bush (for browsing), <strong>the</strong> selective grazing<br />

habits of many game species, social behaviour (home range <strong>and</strong> territoriality) <strong>and</strong> also <strong>the</strong> restrictions of a<br />

40


one-camp system (lack of control over animal movements), are taken into consideration in <strong>the</strong> calculation<br />

of <strong>the</strong> economic carrying capacity for game.<br />

The grazing capacity for livestock is given in large animal units per hectare or hectares per large animal<br />

unit (LAU). One large animal unit is regarded as a steer of 450 kg. Conversion values to convert from<br />

game to large animal units or vice versa are used (see Table 12) <strong>and</strong> on <strong>the</strong> basis of <strong>the</strong> metabolizable<br />

energy requirements <strong>and</strong> probable food intake of <strong>the</strong> animals, comparisons are <strong>the</strong>n made in large animal<br />

units. For example a value of 6.03 impala is given as equivalent to one large animal unit.<br />

However, because <strong>the</strong> conversion table does not take into account <strong>the</strong> differences in food <strong>and</strong> habitat<br />

preferences of <strong>the</strong> different game species, <strong>the</strong> diversity in <strong>vegetation</strong> <strong>types</strong>, <strong>the</strong>ir <strong>condition</strong> <strong>and</strong> production,<br />

availability of browse <strong>and</strong> grazing, <strong>and</strong> accessibility of <strong>the</strong> terrain, <strong>the</strong>se tables should be used with<br />

circumspection <strong>and</strong> only as a broad <strong>and</strong> general guideline. Never<strong>the</strong>less, it is a practical method with<br />

which <strong>the</strong> different habitat <strong>types</strong> on a game ranch can be compared to estimate <strong>the</strong> potential economic<br />

carrying capacity of <strong>the</strong> ranch.<br />

The predictive value of this approach can be enhanced with an intensive study of <strong>the</strong> habitats on a game<br />

ranch, which includes surveys of <strong>the</strong> <strong>veld</strong> <strong>condition</strong> <strong>and</strong> grass <strong>and</strong> browse production of each of <strong>the</strong>se<br />

habitats. The area covered by each habitat <strong>and</strong> its suitability for different game species should be<br />

included when determining grazer/browser capacity. Varying rainfall influences range <strong>condition</strong> <strong>and</strong><br />

frequent assessments are essential to assist in management decisions.<br />

Results <strong>and</strong> discussion<br />

The total economic carrying capacity for <strong>Maremani</strong> was calculated from <strong>the</strong> economic capacities of <strong>the</strong><br />

individual plant communities, excluding communities 1 (rocky outcrops) <strong>and</strong> 17 (riverine areas) (Table 12).<br />

The present economic capacity with a mean annual rainfall of 340 mm is calculated as 39.2 ha/LAU for<br />

game. The area will be able to support a high number of browsers as browsing material is in abundance.<br />

However, it should be emphasized that <strong>the</strong> carrying capacity decreases drastically during prolonged<br />

periods of drought. The carrying capacity according to <strong>the</strong> previous Department of Agriculture was 17<br />

ha/LAU, but presently <strong>the</strong> Limpopo extention officers prescribe a stocking rate of 25 ha/LAU.<br />

The <strong>veld</strong> <strong>condition</strong> <strong>and</strong> economic capacities for <strong>the</strong> individual plant communities are discussed below:<br />

Communities 1 (rocky outcrops) <strong>and</strong> 17 (riverine <strong>vegetation</strong>) are not included. A <strong>veld</strong> <strong>condition</strong> index lower<br />

than 45%, reflects a low grass cover, unpalatable grasses, low biomass production <strong>and</strong> annual grass<br />

species, <strong>and</strong> consequently indicates <strong>veld</strong> in poor <strong>condition</strong> for grazing species. Veld in good <strong>condition</strong><br />

should have an index of higher than 60%, with a high grass cover <strong>and</strong> a high presence of perennial<br />

41


Decreaser, Increaser 1 <strong>and</strong> some Increaser 2a species.<br />

2. Androstachys johnsonii - Terminalia sericea s<strong>and</strong>stone hills<br />

(Lebombo iron wood - Silver cluster-leaf s<strong>and</strong>stone hills)<br />

This community covers approximately 491 ha <strong>and</strong> has a <strong>veld</strong> <strong>condition</strong> index of 48.6% (Table 12). The<br />

mean grass cover is only 15% <strong>and</strong> <strong>the</strong> presence of mostly Decreaser <strong>and</strong> Increaser 2a species indicates<br />

that <strong>the</strong> area is in moderate <strong>condition</strong>. The high percentage rock cover contributes to <strong>the</strong> low grass cover.<br />

The economical capacity for this <strong>veld</strong> is 25 ha/LAU for game.<br />

3. Combretum apiculatum - Danthoniopsis dinteri - Tricholaena monachne rocky outcrops<br />

(Red bushwillow - Mountain grass - Blue-seed grass rocky outcrops)<br />

This community covers approximately 763 ha <strong>and</strong> has a <strong>veld</strong> <strong>condition</strong> index of 44.7% (Table 12). The<br />

mean grass cover is only 11% <strong>and</strong> although some Decreaser species occur, <strong>the</strong> high presence of<br />

Increaser 2a, 2b <strong>and</strong> 2c species indicates that <strong>the</strong> community is in a relatively poor <strong>condition</strong> for grazers.<br />

This is due to ei<strong>the</strong>r high grazing pressure <strong>and</strong>/or <strong>the</strong> result of frequent droughts. The high percentage<br />

rock cover contributes to <strong>the</strong> low grass cover. Unpalatable grass species are also associated with s<strong>and</strong>y<br />

soils. The grazing capacity for this <strong>veld</strong> is 51.7 ha/LAU for game.<br />

4. Colophospermum mopane - Xerophyta viscosa open to dense bush<strong>veld</strong> on low hills <strong>and</strong><br />

rocky outcrops<br />

(Mopane - Xerophyta viscosa open to dense bush<strong>veld</strong> <strong>and</strong> low hills <strong>and</strong> rocky outcrops)<br />

This community covers about 1398 ha <strong>and</strong> is in poor <strong>condition</strong> with a <strong>veld</strong> <strong>condition</strong> index of only 31.7%<br />

(Table 12). The mean grass cover is only 15% <strong>and</strong> <strong>the</strong> high presence of Increaser 2a <strong>and</strong> 2c species<br />

indicates that <strong>the</strong> area has been over-utilized <strong>and</strong>/or subjected to frequent droughts. The high percentage<br />

rock cover contributes to <strong>the</strong> low grass cover. The grazing capacity for this <strong>veld</strong> is 56.6 ha/LAU for game.<br />

5. Colophospermum mopane - Terminalia prunioides - Psiadia punctulata bush<strong>veld</strong><br />

(Mopane - Low<strong>veld</strong> cluster-leaf - Psiadia bush<strong>veld</strong><br />

This community covers about 893 ha <strong>and</strong> is in poor <strong>condition</strong> with a <strong>veld</strong> <strong>condition</strong> index of 37.9% (Table<br />

12). The mean grass cover is 15% <strong>and</strong> <strong>the</strong> high presence of Increaser 2c species indicates that <strong>the</strong> area<br />

has been over-utilized <strong>and</strong>/or subjected to frequent droughts. The grazing capacity for this <strong>veld</strong> is 38.5<br />

ha/LAU for game.<br />

42


6. Sclerocarya birrea - Aristida stipitata - Eragrostis lehmanniana open grass <strong>and</strong> bush<strong>veld</strong><br />

(Marula - Long-awned three-awn - Lehmann’s love grass open grass <strong>and</strong> bush<strong>veld</strong>)<br />

This community covers about 1106 ha <strong>and</strong> has a <strong>veld</strong> <strong>condition</strong> index of 50.5% (Table 12). The mean<br />

grass cover is 66% <strong>and</strong> <strong>the</strong> presence of mostly Decreaser <strong>and</strong> Increaser 2a species indicates that <strong>the</strong><br />

area is in moderate to good <strong>condition</strong>. The grazing capacity for this <strong>veld</strong> is 11.8 ha/LAU for game.<br />

7. Colophospermum mopane - Kirkia acuminata - Acacia erubescens plains bush<strong>veld</strong> <strong>and</strong><br />

woodl<strong>and</strong><br />

(Mopane - White syringa - Blue thorn plains bush<strong>veld</strong> <strong>and</strong> woodl<strong>and</strong>)<br />

This community covers approximately 6630 ha <strong>and</strong> is in a very poor <strong>condition</strong> for grazers with a <strong>veld</strong><br />

<strong>condition</strong> index of only 26.3% (Table 12). The mean grass cover is 15% <strong>and</strong> <strong>the</strong> high presence of<br />

Increaser 2c species indicates that <strong>the</strong> area has been severely over-utilized <strong>and</strong>/or subjected to frequent<br />

droughts. The grazing capacity for this <strong>veld</strong> is 83.7 ha/LAU for game, indicating <strong>the</strong> poor <strong>condition</strong> of this<br />

<strong>vegetation</strong> type.<br />

8. Colophospermum mopane - Boscia albitrunca - Terminalia prunioides open to dense<br />

bush<strong>veld</strong> on plains <strong>and</strong> low rocky hills<br />

(Mopane - Shepherd’s tree - Low<strong>veld</strong> cluster-leaf open to dense bush<strong>veld</strong> on plains <strong>and</strong><br />

low rocky hills)<br />

This community covers about 9813 ha <strong>and</strong> is in a poor <strong>condition</strong> for grazers with a <strong>veld</strong> <strong>condition</strong> index of<br />

33.8% (Table 12). The mean grass cover is 20% <strong>and</strong> <strong>the</strong> high presence of Increaser 2a, 2b <strong>and</strong> 2c<br />

species indicates that <strong>the</strong> area has been over-utilized <strong>and</strong>/or subjected to frequent droughts. The grazing<br />

capacity for this <strong>veld</strong> is 35.1 ha/LAU for game.<br />

9. Colophospermum mopane - Catophractes alex<strong>and</strong>ri - Vernonia cinarescens low <strong>and</strong> dense<br />

bush<strong>veld</strong><br />

(Mopane - Trumpet thorn - Vernonia low <strong>and</strong> dense bush<strong>veld</strong>)<br />

This community covers about 7000 ha <strong>and</strong> is in a poor <strong>condition</strong> for grazers with a <strong>veld</strong> <strong>condition</strong> index of<br />

33.4% (Table 12). The mean grass cover is 20% <strong>and</strong> <strong>the</strong> high presence of Increaser 2a, 2b <strong>and</strong> 2c<br />

species <strong>and</strong> bare soil indicates that <strong>the</strong> area has been severely over-utilized <strong>and</strong>/or is very sensitive to<br />

frequent droughts. The grazing capacity for this <strong>veld</strong> is 36 ha/LAU for game, indicating <strong>the</strong> poor <strong>condition</strong><br />

43


of this <strong>vegetation</strong> type.<br />

10. Colophospermum mopane - Sesamothamnus lugardii - Acacia tortilis open to dense low<br />

bush<strong>veld</strong><br />

(Mopane - Transvaal sesame bush - Umbrella thorn open to dense low bush<strong>veld</strong>)<br />

This community covers about 1461 ha <strong>and</strong> has a <strong>veld</strong> <strong>condition</strong> index of 44.1% (Table 12). The mean<br />

grass cover is 23% <strong>and</strong> <strong>the</strong> fairly high percentage Decreaser <strong>and</strong> Increaser 2a species, indicates that <strong>the</strong><br />

area is in poor to moderate <strong>condition</strong>. The grazing capacity for this <strong>veld</strong> is 19.7 ha/LAU for game.<br />

11. Colophospermum mopane - Gardenia resiniflua - Tetrapogon tenellus thicket<br />

(Mopane - Resin gardenia - Tetrapogon thicket)<br />

This community covers about 418 ha <strong>and</strong> has a <strong>veld</strong> <strong>condition</strong> index of 48.3%, indicating <strong>veld</strong> in moderate<br />

good <strong>condition</strong>. Although a high percentage Decreasers occurs in this community, <strong>the</strong> mean grass cover<br />

is however only 11% <strong>and</strong> contributes to <strong>the</strong> relatively low grazing capacity of 40.3 ha/LAU.<br />

12. Colophospermum mopane - Aristida adscensionis bush<strong>veld</strong><br />

(Mopane - Nine-awned grass bush<strong>veld</strong><br />

This community covers approximately 2041 ha <strong>and</strong> has a <strong>veld</strong> <strong>condition</strong> index of 24.1% (Table 12). The<br />

grass cover is only 14% <strong>and</strong> <strong>the</strong> very high presence of Increaser 2c species indicates that this area has<br />

been severely over-utilized <strong>and</strong>/or is very sensitive to frequent droughts. The carrying capacity for this<br />

<strong>veld</strong> is 124 ha/LAU for game.<br />

13. Colophospermum mopane - Acacia tortilis - Eragrostis lehmanniana low dense bush<strong>veld</strong><br />

(Mopane - Umbrella thorn - Lehmann’s love grass low dense bush<strong>veld</strong>)<br />

This community covers about 1738 ha. The <strong>veld</strong> <strong>condition</strong> index is poor at 29.7% <strong>and</strong> with a grass cover<br />

of 12% <strong>and</strong> high percentages of Increaser 2a <strong>and</strong> 2c species, <strong>the</strong> carrying capacity is a low 81.7 ha/LAU.<br />

14. Acacia tortilis - Eragrostis lehmanniana old fields<br />

(Umbrella thorn - Lehmann’s love grass old fields)<br />

This area covers about 460 ha <strong>and</strong> is in poor <strong>condition</strong> with a <strong>veld</strong> <strong>condition</strong> index of only 34.4%. The<br />

mean grass cover is 24% <strong>and</strong> <strong>the</strong> high presence of Increaser 2a <strong>and</strong> 2c species indicates that <strong>the</strong> area<br />

44


has been disturbed <strong>and</strong> over-utilized in <strong>the</strong> past. The grazing capacity for this <strong>veld</strong> is 32.8 ha/LAU for<br />

game.<br />

15. Pechuel-loeschia leubnitziae - Urochloa mosambicensis open grassl<strong>and</strong> to dense<br />

bush<strong>veld</strong><br />

(Wild sage - Common signal grass open grassl<strong>and</strong> to dense bush<strong>veld</strong>)<br />

This area covers about 260 ha. The <strong>veld</strong> <strong>condition</strong> index is fairly high at 50.8%, indicating <strong>veld</strong> in<br />

moderate to good <strong>condition</strong> in places. The grass cover is also high at 79% <strong>and</strong> <strong>the</strong> relatively high<br />

presence of Decreaser <strong>and</strong> Increaser 2b species indicates light to moderately utilized <strong>veld</strong>. The grazing<br />

capacity for this <strong>veld</strong> is 12.3 ha/LAU, <strong>the</strong> highest of all <strong>the</strong> communities.<br />

16. Combretum imberbe - Philenoptera violacea stream community<br />

(Leadwood - Apple-leaf stream community)<br />

This area covers approximately 210 ha <strong>and</strong> has a <strong>veld</strong> <strong>condition</strong> index of 43.4% (Table 12). The mean<br />

grass cover is 49% <strong>and</strong> because no Increaser 2c species were recorded, <strong>the</strong> grazing capacity for this <strong>veld</strong><br />

is relatively high at 15.8 ha/LAU for game. The high Increaser 2a <strong>and</strong> 2b species indicates some<br />

moderately utilized <strong>veld</strong>.<br />

Alternative approaches to determine economic carrying capacity<br />

O<strong>the</strong>r methods can be used to estimate short <strong>and</strong> long-term economic carrying capacities. These<br />

methods were developed in savanna regions of South Africa.<br />

Combined <strong>veld</strong> <strong>condition</strong> <strong>and</strong> rainfall method (Danckwerts 1989)<br />

The model was developed in <strong>the</strong> Eastern Cape:<br />

GC = {-0.03 +0.00289 x (X1) + [(X2 - 419.7) x 0.000633]}<br />

where: GC = grazing capacity in large stock units per hectare (LAU/ha)<br />

X1 = percentage <strong>veld</strong> <strong>condition</strong> score<br />

X2 = mean annual rainfall (mm)<br />

45


The above model requires sample site <strong>veld</strong> <strong>condition</strong> scores to be expressed as percentages of a<br />

benchmark <strong>veld</strong> <strong>condition</strong> score. Because of <strong>the</strong> present fairly poor <strong>veld</strong> <strong>condition</strong> of <strong>the</strong> area it was not<br />

possible to use a reference or benchmark sample area. When <strong>the</strong> <strong>veld</strong> <strong>condition</strong> indices given in Table 12<br />

were used, <strong>the</strong> average economic grazing capacity for <strong>Maremani</strong> was calculated as 40.7 ha/LAU. The<br />

grazing capacity between communities varied from 15.1 to 185 ha/LAU. The herbaceous layer in<br />

communities 7 <strong>and</strong> 12 are in such a poor <strong>condition</strong> that this model indicates a zero grazing capacity.<br />

Herbaceous phytomass method (Moore & Odendaal 1987)<br />

The stocking rate for grazer species is calculated from herbaceous phytomass data <strong>and</strong> <strong>the</strong> method was<br />

developed in <strong>the</strong> eastern Kalahari Thorn<strong>veld</strong>:<br />

SR = phytomass (kg/ha) x 0.35 b /10 bb x 365 bbb<br />

where: SR = stocking rate in large stock units per hectare per year<br />

b = utilisation factor: only 35% of <strong>the</strong> herbaceous material is grazed while<br />

40% remains as tufts <strong>and</strong> stubbles <strong>and</strong> 25% is lost to environmental<br />

factors<br />

bb = 10 kg feed per day is required per large stock unit<br />

bbb = number of days in a year<br />

The phytomass of <strong>the</strong> herbaceous layer was determined with <strong>the</strong> Disc-Pasture Meter (Trollope & Potgieter<br />

1986) during 2001 following a good rainy season. The grass biomass after <strong>the</strong> relatively dry 2002 season<br />

was very poor to non-existent.<br />

Disc Pasture Meter measurements for <strong>Maremani</strong> are summarised in Table 10 <strong>and</strong> <strong>the</strong> variations<br />

measured indicated. Community 1 was not measured due to <strong>the</strong> high rockiness. In parts of <strong>the</strong> o<strong>the</strong>r<br />

communities where <strong>the</strong> grass cover was minimal, no measurements could be taken. The flood plains in<br />

<strong>the</strong> south of Solitude recorded up to 7 800 kg/ha. Within a community, grass biomass showed large<br />

spatial variation. The grazing capacity for <strong>Maremani</strong> according to this method is approximately 48<br />

ha/LAU.<br />

Rainfall method (Coe, Cumming & Phillipson 1976)<br />

A significant relationship was found r² = 0.94, P < 0.001) between rainfall (range: 165 to 650 mm) <strong>and</strong><br />

large herbivore biomass (range: 405 to 4 848 kg/km²). The equation that was derived for wildlife areas<br />

receiving less than 650 mm rainfall annually, was:<br />

46


Large Herbivore Biomass (kg/km²) = 8.684 x (mean annual rainfall) - 1205.9<br />

The herbivore biomass data included game census data from east <strong>and</strong> sou<strong>the</strong>rn Africa <strong>and</strong> a wide range<br />

of <strong>the</strong> most common large African grazers <strong>and</strong> browsers. Herbivore biomass estimates obtained from <strong>the</strong><br />

above equation would <strong>the</strong>refore represent first approximations of <strong>the</strong> combined grazing <strong>and</strong> browsing<br />

capacity of an area. Shortcomings of this approach are that <strong>the</strong> broad relationship between biomass <strong>and</strong><br />

rainfall does not take into account local temporal <strong>and</strong> spatial variations in <strong>the</strong> habitats. Fur<strong>the</strong>rmore, <strong>the</strong><br />

model was based on animal numbers obtained from a wide variety of count methods.<br />

According to this equation, <strong>the</strong> Large Herbivore Biomass for <strong>Maremani</strong> is 1747 kg/km². <strong>Maremani</strong> covers<br />

about 366 km², which gives a total of 639 402 kg. In terms of LAU this converts to 1 421 LAU. This is<br />

about 38% higher than calculated with <strong>the</strong> Ecological Index method (884 LAU). If <strong>the</strong> total area of 36583<br />

ha is used in <strong>the</strong> calculations, an economic carrying capacity of 25.7 ha/LAU is derived.<br />

! Large animal unit (LAU) <strong>and</strong> Browser Unit method of Snyman (1991), related to rainfall<br />

Stocking rates for animals in terms of LAU’s <strong>and</strong> BU’s, based on mean annual rainfall, are given by<br />

Snyman (1991) in Table 11. Accordingly <strong>the</strong> stocking rate for grazers on <strong>Maremani</strong> should be<br />

approximately 2.72 LAU/100 ha or 36.8 ha/LAU, which is comparable to <strong>the</strong> value of 39.2 ha/LAU found<br />

for <strong>Maremani</strong> with <strong>the</strong> Ecological Index method (Table 12). The browsing capacity according to Table 11<br />

is approximately 9.0 BU/100 ha (see following method <strong>and</strong> Table 16).<br />

Browsing capacity<br />

Browse is <strong>the</strong> sum total of woody plant material that is potentially edible to a specific set of animals in a<br />

specific area. The term available browse is a more restricted quantity <strong>and</strong> includes all <strong>the</strong> leaves, twigs,<br />

bark, flowers <strong>and</strong> pods that are within reachable height of a given type of animal species. The browsable<br />

volume is usually limited to <strong>the</strong> foliage up to 2 m for most browsers, <strong>and</strong> up to 5.5 m for giraffe <strong>and</strong><br />

elephant.<br />

The available browse on a game ranch is influenced by:<br />

$ <strong>the</strong> density of woody plants;<br />

$ <strong>the</strong> amount of leaf material within reach of an animal;<br />

$ <strong>the</strong> species composition of <strong>the</strong> woody <strong>vegetation</strong>;<br />

47


$ <strong>the</strong> palatability <strong>and</strong> digestibility of <strong>the</strong> woody <strong>vegetation</strong> for example tannin content;<br />

$ <strong>the</strong> growth potential of woody species;<br />

$ phenology of woody species;<br />

$ chemical defences of woody plants e.g. condensed tannins;<br />

$ structural defences e.g. thorns.<br />

Browsers are limited by food supply ra<strong>the</strong>r than o<strong>the</strong>r factors such as territoriality. They will starve to<br />

death before <strong>the</strong>y kill <strong>the</strong>ir resource. The browse supply in <strong>the</strong> late dry season imposes a limit on <strong>the</strong><br />

stocking rate for browsers. Kudu mortalities in Limpopo have been attributed to sudden cold spells<br />

(pneumonia), disease (anthrax) <strong>and</strong> very important, <strong>the</strong> lack of evergreen palatable plant species for <strong>the</strong><br />

animals to survive <strong>the</strong> late dry season (low resource availability).<br />

The browsing capacity of a given area indicates <strong>the</strong> area’s potential to carry a certain number of animals<br />

in a healthy productive <strong>and</strong> reproductive <strong>condition</strong> over a prolonged period of time, without <strong>the</strong><br />

deterioration of <strong>the</strong> resources. The browsing capacity for game farms should ideally be determined<br />

separately from <strong>the</strong> grazer component. Browsing capacity is defined in terms of <strong>the</strong> number of browser<br />

units that can be carried per hectare (BU/ha). A browser unit (BU) is taken as <strong>the</strong> equivalent of a 140kg<br />

browser.<br />

Large animal units (LAU’s) <strong>and</strong> browser unit (BU) replacement values (or equivalents) can be used to<br />

calculate <strong>the</strong> browsing capacity for an area. In Table 14 <strong>the</strong> LAU <strong>and</strong> BU unit conversions for game<br />

species are given.<br />

The application of only <strong>the</strong> agricultural LAU concept does not allow for <strong>the</strong> ecological separation of<br />

herbivorous ungulates <strong>and</strong> thus overlooks <strong>the</strong> potential for using <strong>the</strong> specialised <strong>and</strong> complementary<br />

resource-use habits of wild ungulates to maximise <strong>veld</strong> utilisation (Snyman 1991; Peel et al. 1994; Dekker<br />

1996, 1997).<br />

An adapted version of <strong>the</strong> LAU/BU method was used to determine <strong>the</strong> present <strong>and</strong> recommended<br />

carrying capacity for <strong>Maremani</strong> (see Tables 12 to 16):<br />

Present carrying capacity:<br />

The total number of LAU’s recommended for grazers is 884 LAU (Table 12). The browsing capacity is<br />

estimated at 8 BU’s per 100 ha (see Table 11), which gives a total of 2927 BU’s. To convert to LAU, <strong>the</strong><br />

BU’s are multiplied by 0.42 (that is <strong>the</strong> LAU value per kudu) for a total of 1229 LAU’s. The total<br />

recommended LAU’s is 2113 LAU’s.<br />

48


The present numbers of game (2000) are given in Table 13 <strong>and</strong> <strong>the</strong> percentage of <strong>the</strong> recommended<br />

capacity calculated per feeding class. The present numbers of game indicate overstocking by<br />

approximately 16% (Table 13).<br />

When <strong>the</strong> grazer <strong>and</strong> browser components are separated according to <strong>the</strong> feeding spectrum of each<br />

animal (Table 14), <strong>the</strong> carrying capacity for grazers is <strong>the</strong>n 34.6 ha/LSU which is higher than <strong>the</strong><br />

calculated capacity of 39.2 ha/LAU. This indicates a 16% overstocking of grazers. The browsing<br />

capacity of 9.1 BU’s per 100 ha is higher than <strong>the</strong> 8.0 BU per 100 ha recommended for <strong>the</strong> area. This<br />

indicates a 23% overstocking of browsers. If <strong>the</strong> browser units are converted to LAU’s, <strong>the</strong> LAU’s for<br />

grazers (1056) <strong>and</strong> browsers (1403) add up 2459 LAU’s, giving a carrying capacity of 14.9 ha/LAU.<br />

However, <strong>the</strong> important aspect is that only 42.9% of this capacity is allocated to grazers.<br />

Recommended carrying capacity:<br />

The recommended percentage ratio of feeding classes as well as <strong>the</strong> recommended numbers of game<br />

are indicated in Table 15. An indication of <strong>the</strong> population growth per annum in terms of animal numbers is<br />

also indicated. The recommended numbers of <strong>the</strong> animalsindicated in Table 15 are <strong>the</strong>n used in Table 16<br />

to calculate <strong>the</strong> grazing <strong>and</strong> browsing capacity. The grazing <strong>and</strong> browsing is separated according to <strong>the</strong><br />

feeding strategies of <strong>the</strong> animals. The grazing capacity is calculated as 41.4 ha/LAU <strong>and</strong> <strong>the</strong> browsing<br />

capacity as 8 BU’s per 100 ha.<br />

If substitution ratios are <strong>the</strong>refore based on metabolic mass only, without consideration of ungulate<br />

species differences in resource utilisation (grazing <strong>and</strong> browsing), stocking density could be<br />

underestimated for an area.<br />

In summary, <strong>the</strong> results from <strong>the</strong> different methods are:<br />

Ecological Index method 39.2 ha/LAU<br />

Veld <strong>condition</strong>/rainfall method 40.7 ha/LAU<br />

Phytomass method 48 ha/LAU<br />

Rainfall method 25.7 ha/LAU<br />

LAU/BU method (Snyman): Grazing 36.8 ha/LAU<br />

LAU/BU method:<br />

Browsing 9.2 BU/100 ha<br />

49


Present capacity: Grazing 34.6 ha/LAU<br />

Browsing 9.1 BU/100 ha<br />

Combined: 14.9 ha/LAU<br />

Recommended capacity: Grazing 41.4 ha/LAU<br />

CHAPTER 7<br />

GAME<br />

Browsing 8.0 BU/100 ha<br />

Combined: 18.6 ha/LAU<br />

Game species that historically occurred in <strong>the</strong> area are Black rhinoceros, Blue wildebeest, Bushbuck,<br />

Bushpig, Buffalo, Grey duiker, El<strong>and</strong>, Giraffe, Grey rhebuck, Hippopotamus, Impala, Klipspringer, Kudu,<br />

Ostrich, Reedbuck, Steenbok, Roan antelope, Sable antelope, Tsessebe, Warthog, Waterbuck, White<br />

rhinoceros <strong>and</strong> Zebra. Species at present on <strong>Maremani</strong> that were not historically from <strong>the</strong> area are<br />

Blesbok, Gemsbok (Oryx) <strong>and</strong> Red hartebeest.<br />

According to <strong>the</strong> present game numbers (based on <strong>the</strong> count of 2001), <strong>the</strong> area is stocked to<br />

approximately 116.1% of its capacity (Table 14). The total area of approximately 36583 ha is used to<br />

recommend animal numbers (Table 15). The total number of 1967 LAU’s is based on <strong>the</strong> grazing<br />

browsing capacity indicated in Table 16.<br />

The recommended game suitable for <strong>Maremani</strong> are Blue wildebeest, Bushbuck, Bushpig, Grey duiker,<br />

50


El<strong>and</strong>, Elephant, Giraffe, Impala, Klipspringer, Kudu, Ostrich, Steenbok, Warthog, Waterbuck, White<br />

rhinoceros <strong>and</strong> Zebra (Table 15). The numbers of each species are also given. Black rhinoceros could be<br />

considered in future. The following aspects should be emphasized:<br />

The introduction of more grazer species such as buffalo, roan antelope, sable antelope <strong>and</strong> tsessebe is<br />

not recommended considering <strong>the</strong> poor <strong>condition</strong> of <strong>the</strong> grass layer.<br />

According to Table 15, provision is made for 9% low-selective or bulk feeders, 13% high selective grazers,<br />

38% mixed grazers/browsers <strong>and</strong> 40% browsers. The low percentage grazers recommended is due to <strong>the</strong><br />

poor <strong>condition</strong> of <strong>the</strong> grass layer <strong>and</strong> at this stage <strong>the</strong> area is more suitable for mixed feeders <strong>and</strong><br />

browsers.<br />

Harvesting, culling or hunting should be introduced to keep <strong>the</strong> populations at economic capacity because<br />

population growth is limited at ecological capacity. Overgrazing also results in animals being more<br />

susceptible to prolonged periods of drought.<br />

51


Management strategy<br />

CHAPTER 8<br />

MANAGEMENT<br />

Due to <strong>the</strong> event-driven <strong>and</strong> unpredictable climate (rainfall), an adaptive management strategy needs to<br />

be implemented. This is necessary to limit mass mortalities of animal species or overgrazing of <strong>the</strong> <strong>veld</strong>.<br />

Related plant communities are grouped to form management units based on relatively homogeneous<br />

<strong>vegetation</strong> <strong>types</strong>, topography, roads <strong>and</strong> rivers (see Figure 8). Existing roads, fences, power-lines, o<strong>the</strong>r<br />

existing infrastructure, inaccessibility of <strong>the</strong> terrain, <strong>and</strong> <strong>the</strong> mosaic distribution pattern of <strong>the</strong> plant<br />

communities are also taken into account in <strong>the</strong> delimitation of <strong>the</strong>se management units. Roads should<br />

ideally separate <strong>the</strong>se units <strong>and</strong> act as firebreaks to prevent <strong>veld</strong> fires from entering <strong>the</strong> area.<br />

The infra-structure needed for an efficient game farm is expensive, for example staff housing <strong>and</strong> game<br />

fencing, <strong>and</strong>, if hunting is introduced, accommodation, abattoir <strong>and</strong> cold room facilities need to be<br />

provided. Poaching may be a problem <strong>and</strong> regular patrols along <strong>the</strong> fence should be undertaken.<br />

Measures should be taken to avoid or minimise selective or patch overgrazing by game through <strong>the</strong> use<br />

of salt blocks <strong>and</strong>/or game licks in areas that are less utilised. The game numbers could be increased or<br />

decreased according to rainfall <strong>and</strong> <strong>veld</strong> <strong>condition</strong> <strong>and</strong> <strong>the</strong>refore live sales, culling <strong>and</strong> hunting (trophy<br />

<strong>and</strong>/or biltong) of game are an intrinsic part of an adaptive management approach.<br />

Game<br />

Game species that occurred historically in <strong>the</strong> area could be re-introduced, preferably from game ranches<br />

in <strong>the</strong> vicinity of <strong>Maremani</strong> or game adapted to <strong>the</strong> same <strong>vegetation</strong> type <strong>and</strong> climate. The off-loading<br />

ramp for game should be as far away from fences, rivers or o<strong>the</strong>r obstacles as possible.<br />

Fire<br />

Fire is not recommended due to <strong>the</strong> low <strong>and</strong> unpredictable rainfall <strong>and</strong> <strong>the</strong> low biomass (fuel load)<br />

available.<br />

Veld <strong>condition</strong><br />

52


The low grass biomass <strong>and</strong> poor species composition indicate <strong>veld</strong> that is not suitable for high numbers of<br />

low <strong>and</strong> high selective grazer species. Veld <strong>condition</strong> <strong>and</strong> carrying capacities need to be monitored as<br />

regularly as possible - at least on an annual basis initially.<br />

It is not only <strong>the</strong> diversity in habitats, geology <strong>and</strong> terrain morphology that contributes to animal diversity,<br />

but also a diversity in <strong>veld</strong> <strong>condition</strong> of an area. Some animals prefer <strong>veld</strong> in good <strong>condition</strong> while o<strong>the</strong>rs<br />

tend to prefer poorer or slightly over-utilised <strong>veld</strong>.<br />

Ecologically sensitive <strong>and</strong>/or problem areas<br />

The riparian <strong>vegetation</strong> along <strong>the</strong> rivers <strong>and</strong> flood plains or wetl<strong>and</strong>s, for example <strong>the</strong> Limpopo, S<strong>and</strong> <strong>and</strong><br />

Njelele Rivers, <strong>and</strong> <strong>the</strong> Mutanga flood plain in <strong>the</strong> sou<strong>the</strong>rn part of Solitude, needs to be conserved.<br />

Aspects such as overgrazing, water withdrawal <strong>and</strong> cultivation (associated with bush clearing) are<br />

threatening this kind of habitat.<br />

Erosion should be monitored <strong>and</strong> measures taken to minimise damage to <strong>the</strong> system. On Solitude some<br />

erosion was visible <strong>and</strong> needs to be monitored or action taken to prevent fur<strong>the</strong>r erosion.<br />

Indicator plant species<br />

Plant species such as Baobab (Adansonia digitata), Shepherd’s tree (Boscia albitrunca), Common star<br />

chestnut (Sterculia rogersii), Sesame bush (Sesamothamnus lugardii), Marula (Sclerocarya birrea) <strong>and</strong><br />

Corkbushes (Commiphora species) should be monitored because <strong>the</strong>y usually show <strong>the</strong> first signs of<br />

over-utilization by browsers <strong>and</strong> elephants.<br />

Licks<br />

Game licks <strong>and</strong> salt blocks should ideally be placed away from <strong>veld</strong> in poor <strong>condition</strong>. Licks can also be<br />

made up using <strong>the</strong> following ingredients:<br />

Lick 1: 50 % coarse salt; 45 % dicalcium phosphate; 5 % Calory-3000 (molasses<br />

powder) <strong>and</strong> optionally some mealie meal.<br />

Lick 2: 50 % coarse salt; 25 % dicalcium phosphate; 20 % Calory-3000 (molasses<br />

powder) <strong>and</strong> 5% ureum. (Ureum should not be used in containers that can not<br />

53


Ticks<br />

drain rain water <strong>and</strong> zebra might have problems with ureum).<br />

Lick 3: 3 - 5 % fish meal; 40 % salt; 50 % dicalcium phosphate; 5 - 8 % Calory 3000; 5 %<br />

mealie meal.<br />

Ticks are apparently not a serious problem in <strong>Maremani</strong>, but some of <strong>the</strong> tick control systems presently<br />

available in <strong>the</strong> game industry include:<br />

1. Duncan Applicator (Tel. (012) 803 6647, Cell 083 263 7897)<br />

2. Tick Off (012) 804 4461, Cell 082 454 0793)<br />

3. Scorpion Dip Applicator ( Parasite Management Systems - Mr. Pierre van Niekerk, (012) 667<br />

4755, Cell 082 853 5405)<br />

Water provision<br />

Permanent water should preferably not be provided in areas that are seasonally dry (winter <strong>and</strong> spring).<br />

Control of indigenous encroacher species<br />

Dense thickets of mopane, sickle bush, umbrella thorn <strong>and</strong> three-hook thorn occur especially on old<br />

cultivated fields. Considering <strong>the</strong> small areas where <strong>the</strong>se species have encroached compared to <strong>the</strong> total<br />

size of <strong>Maremani</strong>, it is not necessary to control indigenous plants.<br />

Alien (exotic) <strong>vegetation</strong><br />

Alien plants should be eradicated.<br />

The following categories have been allocated to declared weeds <strong>and</strong> invader plants (Amendment to <strong>the</strong><br />

regulations of <strong>the</strong> Conservation of Agricultural Resources Act No. 43 of 1983 - see Regulation 15).<br />

Category 1 plants: They are prohibited <strong>and</strong> must be controlled by <strong>the</strong> l<strong>and</strong> user.<br />

Achyran<strong>the</strong>s aspera (Burweed), Argemone ochroleuca (Mexican poppy), Agave<br />

americana (Sisal), Ageratum conyzoides (Ageratum), Datura ferox (Large thorn<br />

54


apple), Datura innoxia (Downy thorn apple), Datura stramonium (Common thorn<br />

apple), Nerium ole<strong>and</strong>er (Ole<strong>and</strong>er), Nicotiana glauca (Wild tobacco), Opuntia<br />

ficus-indica (Sweet prickly pear), Opuntia cf. aurantiaca (Jointed cactus),<br />

Xanthium strumarium (Large cocklebur),<br />

Category 2 plants: These are plants that serve a commercial purpose, e.g. shelterbelt, building<br />

material, animal fodder, medicinal function etc. Plants may be grown <strong>and</strong><br />

maintained in demarcated areas provided that <strong>the</strong>re is a permit <strong>and</strong> that steps are<br />

taken to prevent <strong>the</strong>ir spread.<br />

Psidium guajava (Guava), Ricinus communis (Castor-oil plant)<br />

Category 3 plants: These are ornamentally used plants. These plants may no longer be planted,<br />

maintained or multiplied. Existing plants may remain, as long as all reasonable<br />

steps are taken to prevent <strong>the</strong> spreading <strong>the</strong>reof. They are not allowed within 30<br />

m of <strong>the</strong> 1:50 year flood line of water courses <strong>and</strong> wetl<strong>and</strong>s.<br />

Melia azedarach (Seringa), Jacar<strong>and</strong>a mimosifolia (Jacar<strong>and</strong>a)<br />

These species should be controlled by mechanical <strong>and</strong>/or chemical means. Mechanical means include<br />

ringbarking (girdling), uprooting, chopping, slashing <strong>and</strong> felling. An axe or chain saw or brush cutter can<br />

be used. Stumps or ringbarked stems should be treated immediately with a chemical weedkiller (see<br />

references below). Follow-up treatment is sometimes needed. More information can be found in:<br />

Bromilow, C. 1995. Problem plants of South Africa. Briza Publications, Pretoria.<br />

Grobler, Hermien, J.B. Vermeulen <strong>and</strong> Van Zyl, Kathy. 2000. A guide to <strong>the</strong> use of herbicides. 17th<br />

edition. National Department of Agriculture. Formeset, Pretoria.<br />

Henderson, L. 2001. Alien weeds <strong>and</strong> invasive plants. Plant Protection Research Institute H<strong>and</strong>book no.<br />

12, Agricultural Research Council, Pretoria.<br />

Ecoguard (Access): (011) 463 6057<br />

Poisonous plants<br />

These species are known to cause poisoning of livestock. However, game species are not necessarily<br />

affected in <strong>the</strong> same way.<br />

55


Dichapetalum cymosum, Solanum incanum, Solanum p<strong>and</strong>uriforme, Gomphocarpus fruticosus, Acacia<br />

caffra, Opuntia ficus-indica, Senecio spp., Melia azedarach<br />

56


CHAPTER 9<br />

MONITORING<br />

Detecting ecological effects or ecological monitoring is <strong>the</strong> purposeful <strong>and</strong> repeated examination of <strong>the</strong><br />

state or <strong>condition</strong> of <strong>the</strong> <strong>vegetation</strong> in relation to external stress. It is <strong>the</strong> frequent testing of differences<br />

between baseline or initial surveys <strong>and</strong> follow-up surveys. Ecological monitoring emphasizes changes in<br />

living organisms <strong>and</strong> not merely in <strong>the</strong> physical environment. A prerequisite in any monitoring programme<br />

are permanent reference sites, representative of what is considered necessary to be monitored <strong>and</strong><br />

depending on <strong>the</strong> method adopted.<br />

A monitoring programme serves as an early warning system to detect changes or trends as a result of<br />

management actions, natural events or those areas where past mismanagement occurred with <strong>the</strong> goal to<br />

adapt management strategies where necessary. On a game ranch certain management actions are<br />

implemented <strong>and</strong> possible changes related to <strong>the</strong>se actions should be monitored over time.<br />

Monitoring is important where changes are possible in <strong>the</strong> natural <strong>veld</strong> due to <strong>the</strong> application of new<br />

management programmes. The <strong>veld</strong> <strong>condition</strong> <strong>and</strong> economic capacity of all plant communities need to be<br />

monitored regularly when <strong>the</strong> number of animals increases, which could lead to overgrazing <strong>and</strong> changes<br />

in plant species composition.<br />

Aspects that need to be monitored are:<br />

1. climate (rainfall);<br />

2. <strong>veld</strong> <strong>condition</strong> in terms of plant species composition, species frequency, density <strong>and</strong>/or cover;<br />

3. economic <strong>and</strong> ecological carrying capacity;<br />

4. <strong>vegetation</strong> structure;<br />

5. <strong>the</strong> effects of water provision;<br />

6. <strong>the</strong> effects of bush encroachment <strong>and</strong> its control;<br />

7. <strong>veld</strong> reclamation measures such as soil erosion control; <strong>and</strong><br />

8. game numbers, population growth, mortalities, game distribution, herd composition <strong>and</strong> birth<br />

rates. It was found that it is better <strong>and</strong> more cost effective to a certain extent to count <strong>the</strong> animals<br />

on a farm every three to four years, but <strong>the</strong>n 2 to even 4 times during that specific year.<br />

Monitoring of <strong>veld</strong> <strong>condition</strong> is essential when adaptive management is applied on a game ranch. The aim<br />

is to determine whe<strong>the</strong>r a change in species composition, <strong>the</strong> ratio of decreasers, increasers <strong>and</strong> invaders<br />

57


<strong>and</strong>/or encroachment by woody species has occurred. Depending on <strong>the</strong> results of monitoring, decisions<br />

regarding changes in management actions can be taken.<br />

Methods<br />

Herbaceous component<br />

The wheel-point or step-point method, where 100 nearest plant records are recorded, is used to determine<br />

<strong>the</strong> plant species composition <strong>and</strong> species frequency, ratio of ecological status classes (decreasers <strong>and</strong><br />

increasers) <strong>and</strong> ecological index (<strong>veld</strong> <strong>condition</strong> score). The nearest individual (forb or grass species) <strong>and</strong><br />

<strong>the</strong> nearest perennial grass are recorded. The annual <strong>and</strong> perennial <strong>vegetation</strong> are recorded separately<br />

to provide for <strong>the</strong> large yearly variation in annual species composition <strong>and</strong> frequency in this arid area. If no<br />

plants are recorded within a 0.5 m radius from <strong>the</strong> point, it is recorded as bare soil.<br />

Biomass production<br />

The disc pasture meter is a suitable method to determine <strong>the</strong> grass production (fuel load) within most of<br />

<strong>the</strong> <strong>vegetation</strong> <strong>types</strong> on Marimani.<br />

Woody component<br />

A plot (transect) of 100 m long <strong>and</strong> 2.5 m wide is surveyed. A 100 m tape is placed on one side of <strong>the</strong><br />

transect. All woody plants (shrubs <strong>and</strong> trees) within <strong>the</strong> transect are identified <strong>and</strong> <strong>the</strong>ir distance from <strong>the</strong><br />

beginning of <strong>the</strong> transect, height, maximum canopy diameter in two directions, height of maximum canopy<br />

diameter measurement, height <strong>and</strong> diameter of lowest leaf material (in two directions) <strong>and</strong> stem diameter<br />

(see field form) are recorded. The number of stems is indicated <strong>and</strong> <strong>the</strong> diameter of <strong>the</strong> thickest stem<br />

measured. Measurements are done per 5 m sections on <strong>the</strong> tape i.e. each 5 x 2.5 m section constitutes a<br />

unit.<br />

An importance value is calculated for each species <strong>and</strong> profile diagrams can be drawn for each of <strong>the</strong><br />

transects.<br />

The collected data are also suitable for <strong>the</strong> BECVOL model (Smit 1996). BECVOL describes <strong>the</strong> woody<br />

component quantitatively by determining <strong>the</strong> leaf volume <strong>and</strong> leaf mass of individual trees, density of <strong>the</strong><br />

woody species <strong>and</strong> to analyse <strong>the</strong> structure of <strong>the</strong> <strong>vegetation</strong>.<br />

58


The BECVOL computer program is used to do <strong>the</strong> following calculations:<br />

Primary calculations (for each individual tree)<br />

Leaf volume, leaf dry mass (DM), ETTE (leaf volume equivalents of a 1.5 m single stem tree),<br />

BTE (leaf mass equivalent of a 1.5 m single stem tree) <strong>and</strong> area covered by <strong>the</strong> canopy.<br />

Secondary calculations:<br />

Values are calculated per hectare e.g. ETTE/ha, BTE/ha, DM/ha, plants/ha <strong>and</strong> CSI (canopied<br />

subhabitat index: canopy diameter of large trees in <strong>the</strong> transect expressed as a % of <strong>the</strong> total<br />

transect area). These values are calculated per species <strong>and</strong> per population. The browse capacity<br />

can also be calculated.<br />

Fixed point photography<br />

This is an essential component of monitoring. By taking photographs of <strong>the</strong> <strong>vegetation</strong> or l<strong>and</strong>scape from<br />

<strong>the</strong> same point at regular intervals, a visual record is obtained which can later be subjected to objective<br />

analysis. The advantages derived from fixed-point photographs include <strong>the</strong> following:<br />

1 They provide a rapid means for assessing short <strong>and</strong> medium term trends in <strong>the</strong> <strong>vegetation</strong>, <strong>and</strong><br />

<strong>the</strong>refore can have predictive value.<br />

2. They provide additional evidence for evaluating <strong>and</strong> interpreting <strong>the</strong> impact of various external<br />

influences on <strong>the</strong> <strong>vegetation</strong>.<br />

3. The method is cheap, easy to apply <strong>and</strong> provides a permanent record for re-examination when<br />

required.<br />

The disadvantage of <strong>the</strong> method is that it is difficult to quantify <strong>the</strong> results <strong>and</strong> <strong>the</strong>refore <strong>the</strong>re is a lack of<br />

statistical analysis.<br />

GPS points<br />

GPS readings should be taken at <strong>the</strong> beginning <strong>and</strong> end point of each transect. A metal stake (dropper) is<br />

hammered into <strong>the</strong> soil at <strong>the</strong> beginning <strong>and</strong> end point of each transect <strong>and</strong> spray painted with red paint.<br />

The approximate positions of <strong>the</strong> plots (transects) should be indicated on a map <strong>and</strong> for each plot a<br />

localised map should be drawn to facilitate finding <strong>the</strong> site in future (Appendix F).<br />

59


ACKNOWLEDGEMENTS<br />

Dr S.C.J. Joubert <strong>and</strong> <strong>the</strong> staff of <strong>Maremani</strong>, especially Ben Ferreira <strong>and</strong> Tommy Fourie are thanked for<br />

guidance, help <strong>and</strong> logistic support. Mapo for his excellent cooking <strong>and</strong> Thomas for helping with <strong>the</strong><br />

surveys. My family for assistance in this project.<br />

60


REFERENCES<br />

ACOCKS, J.P.H. Veld <strong>types</strong> of South Africa. Mem. Bot. Surv. S. Afr. 57: 1-146.<br />

BOTHMA, J. DU P. (Ed). 1996. Game ranch management. J.L. van Schaik, Pretoria.<br />

BROMILOW, C. 1995. Problem plants of South Africa. Briza Publications, Pretoria.<br />

COE, M.J., D.H. CUMMING & PHILLIPSON. 1976. Biomass <strong>and</strong> production of large African herbivores in<br />

relation to rainfall <strong>and</strong> primary production. Oecologia 22: 341 354.<br />

DANCKWERTS, J.E. 1989. Sweet<strong>veld</strong>. In: DANCKWERTS, J.E. & TEAGUE, W.R. (Eds.). Veld<br />

management in <strong>the</strong> Eastern Cape. Department of Agriculture <strong>and</strong> Water Supply. Government<br />

Printer, Pretoria. pp. 140 - 148.<br />

DEKKER, B. 1996. Ekologiese skeiding tussen groot herbivore van die Messina-proefplaas,<br />

Limpopovallei. MSc verh<strong>and</strong>eling, Universiteit van Pretoria.<br />

DEKKER, B. 1997. Calculating stocking rates for game ranches: substitution ratios for use in <strong>the</strong> Mopani<br />

Veld. Afr. J. Range & Forage Sci. 14:62 - 67.<br />

DUBEL. 2000. Resource inventory. Integrated Environmental Services.<br />

ERASMUS, J.F. 1987. Rainfall deciles for Transvaal Region. S.I.R.I., Department of Agriculture <strong>and</strong> Water<br />

supply. Pretoria.<br />

GROBLER, HERMIEN, J.B. VERMEULEN <strong>and</strong> VAN ZYL, KATHY. 2000. A guide to <strong>the</strong> use of herbicides.<br />

17th edition. National Department of Agriculture. Formeset, Pretoria.<br />

HENDERSON, L. 2001. Alien weeds <strong>and</strong> invasive plants. Plant Protection Research Institute H<strong>and</strong>book<br />

no. 12, Agricultural Research Council, Pretoria.<br />

KELLERMAN, T.S., COETZER, J.A.W. & NAUDE, T.W. 1988. Plant poisonings <strong>and</strong> mycotoxicoses of<br />

livestock in sou<strong>the</strong>rn Africa. Oxford University Press, Cape Town.<br />

LAND TYPE MAPS. I.C.S.W. Government Printer, Pretoria.<br />

LOW, A & REBELO, A. 1998. Vegetation of South Africa, Lesotho <strong>and</strong> Swazil<strong>and</strong>. Department of<br />

Environmental Affairs & Tourism, Pretoria.<br />

MOORE, A. & A. ODENDAAL. 1987. Die ekonomiese implikasies van bosverdigting en bosbeheer soos<br />

van toepassing op ‘n speenkalfproduksiestelsel in die doringbos<strong>veld</strong> van die Molopogebied. J.<br />

Grassl. Soc. Sth. Afr. 4: 139 - 142.<br />

PEEL, M. J.C., PAUW, & D.D. SNYMAN. 1994. The concept of grazer <strong>and</strong> browser animal units for<br />

African savanna areas. Bull. Grassl. Soc. S. Afr. 5: 61.<br />

SCHMIDT, A.G., G.K. THERON & W. VAN HOVEN. 1995. A comparison of some methods used to<br />

estimate <strong>the</strong> grazing capacity of a game ranch in Nor<strong>the</strong>rn Province, South Africa. Koedoe 38:<br />

123 - 128.<br />

SNYMAN, D.D. 1991. Drakragnorme vir wildplase in die Mopanie<strong>veld</strong>, noord van die Soutpansberg.<br />

Navorsingsentrum vir Weiding. Departement van L<strong>and</strong>bou-ontwikkeling.<br />

61


TROLLOPE, W.S.W. & A.L.F. POTGIETER. 1986. Estimating grass fuel loads with a disc pasture meter in<br />

<strong>the</strong> Kruger National Park. J. Grassl. Soc. Sth. Afr. 3: 148 - 152.<br />

VAN OUDTSHOORN, F. 1999. Guide to grasses of sou<strong>the</strong>rn Africa. Briza, Pretoria.<br />

VAN WYK, A.E. & P. VAN WYK. 1997. Field guide to trees of sou<strong>the</strong>rn Africa. Struik, Cape Town.<br />

VORSTER, M. 1982. The development of <strong>the</strong> Ecological Index Method for assessing range <strong>condition</strong> in<br />

<strong>the</strong> Karoo. Proc. Grassld Soc. S. Afr. 17: 84 -89.<br />

WEATHER BUREAU. 1988. Climate of South Africa. WB 40. Government Printer, Pretoria.<br />

62


APPENDIX A<br />

PLANT SPECIES LIST<br />

The list is compiled from own surveys, <strong>the</strong> list from <strong>the</strong> PRECIS data bank at <strong>the</strong> National Herbarium,<br />

National Botanical Institute, <strong>and</strong> species identified in <strong>the</strong> report of DUBEL.<br />

The following plant species were recorded on <strong>Maremani</strong> <strong>and</strong> closely surrounding areas. Approximately 71<br />

tree species, 92 shrub species, 76 grass species, 7 sedge species, 9 geophytes, 30 succulents, 6<br />

parasites, 2 palm species, 2 fern species, 290 forb species <strong>and</strong> 14 alien species are listed. This<br />

represents a total of 599 species. It should be remembered that this list is not complete <strong>and</strong> collections<br />

should be made over all seasons to increase <strong>the</strong> present preliminary list.<br />

Trees<br />

Acacia caffra Common hook thorn Gewone haakdoring<br />

Acacia erioloba Camel thorn Kameeldoring<br />

Acacia erubescens Blue thorn Blouhaak<br />

Acacia gr<strong>and</strong>icornuta Horned thorn Horingdoring<br />

Acacia luederitzii False Umbrella thorn Basterhaak-en-steek<br />

Acacia nigrescens Knob thorn Knoppiesdoring<br />

Acacia robusta subsp. clavigera Brack thorn Brakdoring<br />

Acacia robusta subsp. robusta Ankle thorn Enkeldoring<br />

Acacia senegal . var. leiorhachis Slender three-hook thorn Slapdoring<br />

Acacia tortilis subsp. heteracantha Umbrella thorn Haak-en-steek<br />

Acacia xanthophloea Fever tree Koorsboom<br />

Adansonia digitata Baobab Kremetart<br />

Afzelia quanzensis Pod-mahogany Peul-mahonie<br />

Albizia adianthifolia Flat-crown Platkroon<br />

Albizia an<strong>the</strong>lmintica Worm-bark false-thorn Wurmbasvalsdoring<br />

Albizia brevifolia Mountain false-thorn Bergvalsdoring<br />

Albizia harveyi Common false-thorn Bleekblaarboom<br />

Albizia versicolor Large-leaved false thorn Grootblaarvalsdoring<br />

Androstachys johnsonii Lebombo iron wood Lebombo ysterhout<br />

Annona senegalensis Wild custard-apple Wildesuikerappel<br />

Berchemia discolor Brown ivory Bruin-ivoor<br />

Berchemia zeyheri Red ivory Rooi ivoor<br />

Boscia albitrunca Shepherd’s tree Witgatboom<br />

Bridelia cathartica Blue sweetberry Blousoetbessie<br />

Cassia abbreviata Sjambokpod Sambokpeul<br />

Colophospermum mopane Mopanie Mopane<br />

Combretum apiculatum Red bushwillow Rooibos<br />

Combretum hereroense Russet bushwillow Kierieklapper<br />

Combretum imberbe Leadwood Hardekool<br />

63


Combretum molle Fluweelboswilg Velvet Bushwillow<br />

Combretum zeyheri Large-fruited bushwillow Raasblaar<br />

Commiphora edulis Rough-leaved corkwood Skurweblaarkanniedood<br />

Commiphora gl<strong>and</strong>ulosa Tall Common Commiphora Gewone kanniedood<br />

Commiphora marlothii Paperbark corkwood Papierbaskanniedood<br />

Commiphora mollis Velvet corkwood Fluweel kanniedood<br />

Commiphora neglecta Green-stem corkwood Groenstam kanniedood<br />

Commiphora pyracanthoides Common Corkwood Gewone kanniedood<br />

Commiphora tenuipetiolata White-stem corkwood Witstamkanniedood<br />

Commiphora viminea Zebra-bark corkwood Sebrabaskanniedood<br />

Croton gratissimus Lavender feverberry Laventelkoorsbessie<br />

Croton megalobotrys Large feverberry Grootkoorsbessie<br />

Diospyros mespiliformis Jackal-berry Jakkalsbessie<br />

Dombeya burgessiae Pink wild pear Persdrolpeer<br />

Ent<strong>and</strong>rophragma caudatum Mountain mahogany Bergmahonie<br />

Ekebergia capensis Cape ash Witessenhout<br />

Faidherbia albida Ana tree Anaboom<br />

Ficus sycomorus Common cluster fig Gewone trosvy<br />

Ficus tettensis Small-leaved rock fig Kleinblaar rotsvy<br />

Garcinia livingstonei African mangosteen Lae<strong>veld</strong>se geelmelkhout<br />

Gyrocarpus americanus Propeller tree Helikopterboom<br />

Kirkia acuminata White seringa Witsering<br />

Lannea discolor Live-long Dikbas<br />

Lannea schweinfurthii var. stuhlmannii False marula Baster maroela<br />

Maerua angolensis Bead-bean tree Knoppiesboontjieboom<br />

Manilkara mochisia Low<strong>veld</strong> milk berry Lae<strong>veld</strong>melkbessie<br />

Olax dissitiflora Small sourplum Kleinsuurpruim<br />

Ozoroa paniculosa Common resin tree Gewone harpuisbos<br />

Pappea capensis Jacket-plum Doppruim<br />

Philenoptera violacea Apple-leaf Appelblaar<br />

Pseudolachnostylis maprouneifolia Kudu berry Koedoebessie<br />

Rothmannia capensis Cape Gardenia Kaapse katjiepiering<br />

Sclerocarya birrea subsp. caffra Marula Maroela<br />

Schotia brachypetala Weeping boer-bean Huilboerboon<br />

Steganotaenia araliacea Carrot tree Geelwortelboom<br />

Sterculia rogersii Common star-chestnut Gewone sterkastaiing<br />

Strychnos madagascariensis Black monkey orage Swart klapper<br />

Terminalia prunioides Low<strong>veld</strong> cluster-leaf Sterkbos<br />

Terminalia sericea Silver cluster leaf Vaalboom, S<strong>and</strong>geelhout<br />

Xanthocercis zambesiaca Nyala tree Njalaboom<br />

Xeroderris stuhlmannii Wing bean Vlerkboon<br />

Ziziphus mucronata Buffalo thorn Blink-blaar-wag-‘n-bietjie<br />

Shrubs<br />

Acacia ataxacantha Flame thorn Vlamdoring<br />

Acacia mellifera subsp. detinens Black thorn Swarthaak<br />

Acacia nebrownii Sticky thorn Kleefdoring<br />

Acacia senegal var. rostrata Three-hook thorn Driehaakdoring<br />

Acacia stuhlmannii Vlei thorn Vleidoring<br />

64


Anisotes rogersii<br />

Balanites pedicellaris Small green thorn Kleingroendoring<br />

Bauhinia galpinii Pride-of-<strong>the</strong>-Cape Vlam-van-de-Kaap<br />

Boscia foetida subsp. rehmanniana Stink shepherd’s tree Stinkwitgat<br />

Bridelia mollis Velvet sweetberry Fluweelsoetbessie<br />

Cadaba aphylla Rooi-storm<br />

Caesalpinia gilliesii<br />

Capparis tomentosa Wooly caper bush Wilde Kapperbos<br />

Catophractes alex<strong>and</strong>ri Trumpet thorn Trompetdoring<br />

Cissus cornifolia<br />

Clerodendrum glabrum Tinder wood Tontelhout<br />

Cocculus hirsutus<br />

Combretum mossambicense Knobbly creeper Knoppiesklimop<br />

Combretum paniculatum Flame creeper Vlamklimop<br />

Commiphora africana Hairy corkwood Harige kanniedood<br />

Commiphora angolensis S<strong>and</strong> corkwood S<strong>and</strong>kanniedood<br />

Commiphora schimperi Glossy-leaved corkwood Blinkblaarkanniedood<br />

Cordia gr<strong>and</strong>icalyx Round-leaved saucer-berry Rondeblaarpieringbessie<br />

Croton menyhartii<br />

Cordia caffra Septee tree Septeeboom<br />

Cordia monoica Snot berry Snotbessie<br />

Croton pseudopulchellus Small lavender fever berry Kleinlaventelkoorsbessie<br />

Dalbergia melanoxylon Zebra wood Sebrahout<br />

Dichapetalum cymosum Poison leaf Gifblaar<br />

Dichrostachys cinerea Sickle bush Sekelbos<br />

Dioscorea cotinifolia Wild yam Olifantsvoet<br />

Diospyros lycioides Bluebush Bloubos<br />

Ehretia amoena S<strong>and</strong>paper bush Skurweblaarbos<br />

Ehretia obtusifolia<br />

Ehretia rigida Puzzle bush Deurmekaarbos<br />

Euclea divinorum Magic quarri Towerghwarrie<br />

Euclea natalensis Natal guarri Natalghwarrie<br />

Euclea poly<strong>and</strong>ra<br />

Ficus abutilifolia Large-leaved rock fig Grootblaarrotsvy<br />

Flacourtia indica Governor’s plum Goewerneurspruim<br />

Flueggea virosa White-berry bush Witbessiebos<br />

Gardenia resiniflua Resin gardenia Harpuiskatjiepiering<br />

Gardenia volkensii Savanna gardenia Bos<strong>veld</strong>katjiepiering<br />

Gossypium herbaceum subsp. africanum Wild cotton Wilde katoen<br />

Grewia bicolor White raison Witrosyntjie<br />

Grewia hexamita Giant raisin Reuse rosyntjie<br />

Grewia flava Velvet raisin Fluweelrosyntjie<br />

Grewia flavescens S<strong>and</strong>paper raison Skurwe rosyntjie<br />

Grewia monticola Silver raisin Vaalrosyntjie<br />

Grewia retinervis Kalahari s<strong>and</strong> raisin Kalahari s<strong>and</strong> rosyntjiebos<br />

Grewia subspathulata<br />

Grewia sulcata<br />

Grewia villosa Mallow raison Malvarosyntjie<br />

Gymnosporia buxifolia Common spike-thorn Gewone pendoring<br />

Gymnosporia pubescens<br />

65


Gymnosporia senegalensis Red spike-thorn Rooipendoring<br />

Halleria lucida Tree fuchsia Notsung<br />

Heteromorpha stenophylla var. transvaalensis<br />

Hexalobus monopetalus Shakama plum Shakamapruim<br />

Hippocratea africana var. richardiana<br />

Hippocratea longipetiolata<br />

Hippocratea parvifolia<br />

Jasminum fluminense<br />

Lannea edulis<br />

Lantana rugosa Bird’s br<strong>and</strong>y Wilde salie<br />

Maerua parvifolia<br />

Markhamia zanzibarica Bell bean tree Klokkiesboontjieboom<br />

Mundulea sericea Cork bush Kurkbas<br />

Nuxia oppositifolia Water elder Watervlier<br />

Obetia tenax Mountain nettle Bergbr<strong>and</strong>netel<br />

Ochna inermis Stunted plane Kreupelrooihout<br />

Pechuel-Loeschea leubnitziae Wild sage<br />

Phyllanthus reticulatus Potato bush Aartappelbos<br />

Pluchea dioscoridis<br />

Plumbago zeylanica Plumbago<br />

Portulacaria afra Porkbush Spekboom<br />

Pouzolzia mixta Soap-nettle Seepnetel<br />

Psiadia punctulata<br />

Psydrax livida Green tree Groenboom<br />

Pyrostria hystrix Porcupine bush Ystervarkbos<br />

Rhigozum zambeziacum Mopane pomegranate Mopaniegranaat<br />

Salvadora australis Narrow-leaved mustard tree Smalblaarmosterdboom<br />

Schotia capitata<br />

Sesamothamnus lugardii Transvaal sesame bush Transvaal sesamebos<br />

Sesbania sesban<br />

Solanum coccineum<br />

Tarenna supra-axillaris Narrow-leaved false bride’s bush Smalblaarbasterbruidsbos<br />

Tinnea rhodesiana<br />

Vangueria infausta Wild medlar Wilde mispel<br />

Vernonia cinerascens<br />

Ximenia americana Blue sourplum Blousuurpruim<br />

Zanthoxylum capense Small knobwood Kleinperdepram<br />

Grasses<br />

Ecological<br />

status<br />

Acracne racemosa<br />

Andropogon gayanus Blue grass Blougras I1<br />

Andropogon shinensis Hairy blue grass Harige blougras I1<br />

Aristida adscensionis Annual three-awn Eenjarige Steekgras I2c<br />

Aristida congesta subsp. congesta Tassel three-awn Katstertsteekgras I2c<br />

Aristida congesta subsp. barbicollis Spreading three-awn Lossteekgras I2c<br />

Aristida meridionalis<br />

Aristida cf. pilgeri<br />

Giant three-awn Langbeensteekgras I2b<br />

66


Aristida rhiniochloa Rough three-awn Skurwesteekgras I2c<br />

Aristida spectabilis I2c<br />

Aristida stipitata Long-awned three-awn Langnaaldsteekgras I2c<br />

Aristida transvaalensis Rock three-awn Klipgras I1<br />

Bothriochloa radicans Stink grass Stinkgras I2b<br />

Brachiaria deflexa False signal grass Vals sinjaalgras D<br />

Brachiaria brizantha Common signal grass Broodsinjaalgras I2a<br />

Brachiaria erusiformis Sweet signal grass Litjiessinjaalgras I2c<br />

Brachiaria nigropedata Black-footed signal grass Swartvoetjiegras D<br />

Cenchrus ciliaris Blue buffalo grass Bloubuffelsgras D<br />

Chloris roxburghiana Plume chloris Pluim chloris I2a<br />

Chloris virgata Fea<strong>the</strong>red grass Witpluimgras I2a<br />

Cynodon dactylon Couch Grass Kweekgras I2c<br />

Dactyloctenium giganteum Giant crowfoot Reuse hoenderspoor I2a<br />

Dactyloctenium aegyptium Common crowfoot Hoenderspoorgras I2c<br />

Danthoniopsis dinteri Mountain grass Berghawer I2a<br />

Digitaria eriantha Finger grass Vingergras D<br />

Digitaria milanjiana<br />

Digitaria sanguinalis Crab finger grass Kruisvingergras<br />

Digitaria seriata<br />

Digitaria velutina Flaccid finger grass Slapvingergras I2a<br />

Diplachne fusca Swamp grass Kuilgras D<br />

Eleusine coracana Goose grass Osgras I2c<br />

Enneapogon cenchroides Nine-awned grass Negenaaldgras I2b<br />

Enneapogon scoparius Bottlebrush grass Kalkgras I2c<br />

Enneapogon spathaceus<br />

Enteropogon macrostachyus Mopane grass Mopaniegras D<br />

Eragrostis annulata<br />

Eragrostis aspera Rough love grass Grootpluim eragrostis I2c<br />

Eragrostis cilianensis Stink love grass I2c<br />

Eragrostis curvula Weeping Love Grass Oul<strong>and</strong>sgras I2b<br />

Eragrostis cylindriflora<br />

Eragrostis gummiflua Gum grass Gomgras I2b<br />

Eragrostis lehmanniana Lehmann’s Love Grass Knietjiesgras I2a<br />

Eragrostis porosa<br />

Eragrostis rigidior Broad-leaved curly leaf Breë krulblaar I2b<br />

Eragrostis rotifer Pearly love grass I2a<br />

Eragrostis superba Saw-too<strong>the</strong>d love grass Weeluisgras I2a<br />

Eragrostis trichophora Hairy love grass Harige pluimgras I2c<br />

Eragrostis viscosa Sticky love grass Klewerige eragrostis I2c<br />

Eriochloa meyeriana Black-footed water grass D<br />

Fingerhuthia africana Thimble grass Vingerhoedgras D<br />

Heteropogon contortus Spear Grass Assegaaigras I2a<br />

Hyper<strong>the</strong>lia dissoluta Yellow thatching grass Geeltamboekiegras I1<br />

Melinis repens Natal Redtop Natal Rooipluim I2b<br />

Oropetium capense Dwarf grass Haasgras I2c<br />

Panicum coloratum White buffalo grass Witbuffelsgras D<br />

Panicum deustum Broad-leaved panicum Breëblaarbuffelsgras D<br />

Panicum maximum Guinea grass Buffelsgras D<br />

Panicum natalense Natal panicum Suurbuffelsgras D<br />

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Phragmites australis Common Reed Fluitjiesriet I2a<br />

Pogonarthria squarrosa Herringbone Grass Sekelgras I2c<br />

Schmidtia pappophoroides S<strong>and</strong> quick S<strong>and</strong>kweek D<br />

Setaria incrassata Vlei Bristle grass Vleimannagras D<br />

Setaria sagittifolia Arrow grass Pylblaargras I2a<br />

Setaria verticillata Bur Bristle grass Klitsgras I2c<br />

Sporobolus consimilis<br />

Sporobolus ioclados Pan dropseed Panfynsaadgras D<br />

Sporobolus panicoides Christmas tree grass Kersboomgras I2a<br />

Sporobolus pyramidalis Catstail dropseed Katstertfynsaadgras I2c<br />

Stipagrostis hirtigluma Blue bushman grass Blouboesmangras I2b<br />

Stipagrostis uniplumis Silky bushman grass Blinkaarboesmangras I2a<br />

Tetrapogon tenellus<br />

Tragus berteronianus Carrot seed grass Wortelsaadgras I2c<br />

Tricholaena monachne Blue-seed grass Blousaadgras I2a<br />

Urochloa mosambicensis Common signal grass Bos<strong>veld</strong>beesgras I2b<br />

Urochloa brachyura<br />

Urochloa panicoides Garden signal grass Tuinbeesgras I2c<br />

Sedges<br />

Bulbostylis hispidula Fynbiesie Slender sedge<br />

Coleochloa pallidior<br />

Cyperus rupestris<br />

Cyperus sexangularis<br />

Kyllinga alba Witbiesie<br />

Mariscus rehmannianus<br />

Schoenoplectus corymbosus<br />

Geophytes<br />

Camptorrhiza strumosa Froetang<br />

Crinum minimum<br />

Crinum buphanoides<br />

Dipcadi papillatum<br />

Gladiolus oatesii<br />

Ledebouria revoluta<br />

Pancratium tenuifolium A<strong>and</strong>blommetjie<br />

Scadoxus multiflorus<br />

Trachy<strong>and</strong>ra saltii<br />

Succulents<br />

Adenia fruticosa subsp. simplicifolia<br />

Adenia rep<strong>and</strong>a<br />

Adenia spinosa Olifantsvoet<br />

Adenium multiflorum Impala lily Impala lelie<br />

Aloe chabaudii<br />

Aloe globuligemma<br />

Aloe littoralis<br />

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Aloe lutescens<br />

Aloe marlothii<br />

Cissus quadrangularis<br />

Cyphostemma segmentatum<br />

Cyphostemma schlechteri<br />

Cyphostemma spinosopilosum<br />

Euphorbia cooperi<br />

Euphorbia malevola<br />

Euphorbia monteiri subsp. ramosa<br />

Euphorbia schinzii<br />

Euphorbia transvaalensis<br />

Hoodia sp. cf. currorii<br />

Huernia zebrina subsp. magniflora<br />

Kleinia longiflora<br />

Monadenium lugardiae<br />

Orbeopsis valida<br />

Sansevieria aethiopica Bowstring hemp Aambeiwortel<br />

Sansevieria hyacinthoides<br />

Sansevieria pearsonii<br />

Sarcostemma viminale<br />

Stapelia gettliffei<br />

Stapelia kwebensis<br />

Tinospora fragosa<br />

Parasites<br />

Alectra orobanchoides<br />

Alectra sessiliflora<br />

Tapinanthus leendertziae Mistle toe Voëlent<br />

Tapinanthus sambesiacus Mistle toe Voëlent<br />

Viscum combreticola Mistle toe Voëlent<br />

Viscum rotundifolium Mistle toe Voëlent<br />

Palms<br />

Hyphaene coriacea Ilala palm Lalapalm<br />

Hyphaene petersiana Real fan palm Opregte waaierpalm<br />

Ferns<br />

Pellaea calomelanos<br />

Selaginella dregei Resurrection selaginella<br />

Forbs<br />

Abutilon angulatum var. macrophyllum<br />

Abutilon angulatum var. angulatum<br />

Abutilon austro-africanum<br />

Abutilon fruticosum<br />

Abutilon gr<strong>and</strong>iflorum<br />

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Abutilon pycnodon<br />

Abutilon ramosum<br />

Abutilon rehmannii<br />

Acalypha indica<br />

Achyran<strong>the</strong>s aspera<br />

Acrotome inflata<br />

Ageratum conyzoides<br />

Alternan<strong>the</strong>ra pungens<br />

Amaranthus thunbergii<br />

An<strong>the</strong>rothamnus pearsonii<br />

Anticharis linearis<br />

Apium graveolens<br />

Aptosimum elongatum<br />

Aptosimum lineare<br />

Aptosimum marlothii<br />

Asparagus africanus<br />

Asparagus aspergillus<br />

Asparagus bechuanicus<br />

Asparagus cooperi<br />

Asparagus nodulosus<br />

Asparagus suaveolens<br />

Barleria affinis<br />

Barleria albostellata<br />

Barleria bremekampii<br />

Barleria cross<strong>and</strong>rifolius<br />

Barleria elegans<br />

Barleria holubii<br />

Barleria lancifolia<br />

Barleria prionitis<br />

Barleria rogersii<br />

Barleria transvaalensis<br />

Barleria senensis<br />

Becium filamentosum<br />

Bergia salaria<br />

Blepharis aspera<br />

Blepharis diversispina<br />

Blepharis pruinosa<br />

Blepharis subvolubilis<br />

Boerhavia coccinea<br />

Boerhavia diffusa<br />

Calostephane divaricata<br />

Caralluma lugardii<br />

Cardiospermum corindum<br />

Cardiospermum halicacabum<br />

Celosia trigyna<br />

Cephalaria pungens<br />

Cerato<strong>the</strong>ca sesamoides<br />

Cerato<strong>the</strong>ca triloba<br />

Chamaecrista absus<br />

Chamaecrista stricta<br />

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Chamaesyce inaequilatera<br />

Chamaesyce neopolycnemoides<br />

Chascanum incisum<br />

Cissampelos mucronata<br />

Cleome angustifolia subsp. petersiana Wild cleome<br />

Cleome oxyphylla<br />

Cleome hirta<br />

Cleome monophylla<br />

Clerodendrum ternatum<br />

Coccinia rehmannii<br />

Commelina benghalensis<br />

Commelina eckloniana<br />

Commelina erecta<br />

Commicarpus helenae<br />

Commicarpus pent<strong>and</strong>rus<br />

Commicarpus pilosus<br />

Commicarpus plumbagineus<br />

Conyza scabrida<br />

Corallocarpus triangularis<br />

Corbichonia decumbens<br />

Corchorus asplenifolius<br />

Corchorus kirkii<br />

Corrigiola litoralis<br />

Crotalaria brachycarpa<br />

Crotalaria damarensis<br />

Crotalaria laburnifolia<br />

Crotalaria schinzii<br />

Crotalaria steudneri<br />

Crotalaria podocarpa<br />

Cucumis africanus Wild cucumber Wilde komkommer<br />

Cucumis zeyheri<br />

Cyathula lanceolata<br />

Dalechampia galpinii<br />

Decorsea schlechteri<br />

Dicerocaryum eriocarpum<br />

Dicerocaryum senecioides<br />

Diclis petiolaris<br />

Dicoma tomentosa<br />

Dissotis princeps<br />

Endostemon tenuiflorus<br />

Endostemon tereticaulis<br />

Erian<strong>the</strong>mum ngamicum<br />

Evolvulus alsinoides<br />

Fadogia homblei<br />

Felicia clavipilosa subsp. transvaalensis<br />

Felicia mossamedensis<br />

Flaveria bidentis<br />

Geigeria acaulis<br />

Geigeria burkei Vermeersiektebossie<br />

Gisekia africana<br />

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Glinus bainesii<br />

Glinus lotoides<br />

Glinus oppositifolius<br />

Gomphostigma virgatum<br />

Harpagophytum procumbens subsp. transvaalense<br />

Harpagophytum procumbens<br />

Helichrysum argyrosphaerum<br />

Helichrysum c<strong>and</strong>olleanum<br />

Helictotrichon turgidulum<br />

Heliotropium ciliatum<br />

Heliotropium giessii<br />

Heliotropium ovalifolium<br />

Heliotropium steudneri<br />

Heliotropium strigosum<br />

Heliotropium zeylanicum<br />

Helixan<strong>the</strong>ra garciana<br />

Hemizygia albiflora<br />

Hemizygia elliottii<br />

Hemizygia petiolata<br />

Hemizygia petrensis<br />

Hermannia gl<strong>and</strong>uligera<br />

Hermannia modesta<br />

Hermannia stellulata<br />

Hermbstaedtia fleckii<br />

Hermbstaedtia linearis<br />

Hermbstaedtia odorata<br />

Hibiscus calyphyllus<br />

Hibiscus engleri<br />

Hibiscus meyeri<br />

Hibiscus micranthus<br />

Hibiscus platycalyx<br />

Hibiscus sidiformis<br />

Hibiscus subreniformis<br />

Hirpicium bechuanense<br />

Hirpicium gorterioides<br />

Holubia saccata<br />

Hybanthus enneaspermus<br />

Hypertelis salsoloides<br />

Indigastrum costatum<br />

Indigofera astragalina<br />

Indigofera bainesii<br />

Indigofera circinnata<br />

Indigofera daleoides<br />

Indigofera filipes<br />

Indigofera flavicans<br />

Indigofera heterotricha<br />

Indigofera ingrata<br />

Indigofera oxalidea<br />

Indigofera schimperi<br />

Indigofera sordida<br />

72


Indigofera torulosa<br />

Indigofera trita<br />

Ipomoea albivenia<br />

Ipomoea crassipes<br />

Ipomoea magnusiana<br />

Ipomoea obscura<br />

Ipomoea tenuipes<br />

Jamesbrittenia huillana<br />

Jatropha spicata<br />

Jatropha zeyheri<br />

Justicia betonica<br />

Justicia flava<br />

Justicia matammensis<br />

Justicia odora<br />

Justicia protracta<br />

Kohautia caespitosa<br />

Kohautia cynanchica<br />

Kyphocarpa angustifolia<br />

Lagarosiphon muscoides<br />

Lagynias lasiantha<br />

Leucas glabrata<br />

Leucas neuflizeana<br />

Limeum fenestratum<br />

Limeum sulcatum<br />

Limeum viscosum<br />

Litogyne gariepina<br />

Lotononis bainesii<br />

Lotononis curtii<br />

Lotus mossamedensis<br />

Marsdenia macrantha<br />

Megalochlamys kenyensis subsp. australis<br />

Megalochlamys revoluta subsp. cognata<br />

Melanospermum foliosum<br />

Melhania acuminata<br />

Melhania forbesii<br />

Melhania rehmannii<br />

Mollugo cerviana<br />

Monechma debile<br />

Monechma divaricatum<br />

Monsonia glauca<br />

Monsonia senegalensis<br />

Neorautanenia amboensis<br />

Nesaea schinzii<br />

Neuracanthus africanus<br />

Nidorella resedifolia<br />

Ocimum americanum<br />

Otholobium polyphyllum<br />

Pachystigma thamnus<br />

Pavonia burchellii<br />

Pegolettia senegalensis<br />

73


Pergularia daemia<br />

Peristrophe cliffordii<br />

Peristrophe decorticans<br />

Petalidium aromaticum<br />

Petalidium aromaticum var. canescens<br />

Petalidium oblongifolium<br />

Phaeoptilum spinosum<br />

Philyrophyllum schinzii<br />

Phyla nodiflora<br />

Phyllanthus burchellii<br />

Phyllanthus maderaspatensis<br />

Phyllanthus parvulus var. garipensis<br />

Phyllanthus pinnatus<br />

Plectranthus tetensis<br />

Plicosepalus kalachariensis<br />

Polygala sphenoptera<br />

Polygonum plebeium<br />

Polypogon monspeliensis<br />

Portulaca kermesina<br />

Priva africana<br />

Pseudoconyza viscosa<br />

Pseudognaphalium luteo-album<br />

Pterodiscus ngamicus<br />

Ptycholobium contortum<br />

Pulicaria scabra<br />

Pupalia lappacea<br />

Rhinacanthus xerophilus<br />

Rhynchosia minima var. prostrata<br />

Rhynchosia minima<br />

Rhynchosia sublobata<br />

Rhynchosia totta<br />

Rhynchosia venulosa<br />

Schizaea pectinata<br />

Secamone parvifolia<br />

Seddera capensis<br />

Seddera suffruticosa<br />

Selago cecilae<br />

Senecio apiifolius<br />

Senecio pleistocephalus<br />

Senna italica subsp. arachoides Wild senna/el<strong>and</strong>’s pea Swartstorm<br />

Sericorema remotiflora<br />

Sericorema sericea<br />

Sesamum alatum Wild sesame Wilde sesame<br />

Sida chrysantha<br />

Sida cordifolia Flannel weed Hartblaartaaiman<br />

Sida dregei<br />

Sida rhombifolia<br />

Solanum coccineum<br />

Solanum incanum<br />

Solanum kwebense<br />

74


Solanum p<strong>and</strong>uriforme Poison apple Gifappel<br />

Solanum renschii<br />

Sphaeranthus peduncularis<br />

Sphedamnocarpus pruriens<br />

Stomatan<strong>the</strong>s africanus<br />

Stomatostemma monteiroae<br />

Streptopetalum serratum<br />

Stylosan<strong>the</strong>s fruticosa<br />

Tavaresia barklyi<br />

Tephrosia limpopoensis<br />

Tephrosia longipes<br />

Tephrosia polystachya<br />

Tephrosia polystachya var. hirta<br />

Tephrosia purpurea<br />

Tephrosia villosa<br />

Thesium mossii<br />

Tieghemia rogersii<br />

Tragia rupestris<br />

Tribulus terrestris Dubbeltjie<br />

Tribulus zeyheri Dubbeltjie<br />

Tricliceras gl<strong>and</strong>uliferum<br />

Typha capensis<br />

Vahlia capensis<br />

Vernonia amygdalina<br />

Vernonia cinerea<br />

Vernonia fastigiata<br />

Vernonia glabra<br />

Vernonia su<strong>the</strong>rl<strong>and</strong>ii<br />

Vigna unguiculata<br />

Wal<strong>the</strong>ria indica<br />

Xenostegia kentrocaulos<br />

Xenostegia palmata<br />

Xerophyta humilus<br />

Xerophyta viscosa<br />

Zornia milneana<br />

Alien (exotic) species<br />

Achyran<strong>the</strong>s aspera Burweed Grootklits<br />

Agave americana Sisal Garingboom<br />

Ageratum conyzoides Ageratum Ageratum<br />

Argemone ochroleuca Mexican poppy Bloudissel<br />

Datura ferox Large thorn apple Grootstinkblaar<br />

Datura innoxia Downy thorn apple Harige stinkblaar<br />

Datura stramonium Common thorn apple Gewone stinkblaar<br />

Jacar<strong>and</strong>a mimosifolia Jacar<strong>and</strong>a Jakar<strong>and</strong>a<br />

Melia azedarach Seringa Maksering<br />

Nerium ole<strong>and</strong>er Ole<strong>and</strong>er Selonsroos<br />

Nicotiana glauca Wild tobacco Wildetabak<br />

Opuntia ficus-indica Sweet pricly pear Turksvy<br />

75


Opuntia aurantiaca Jointed cactus Litjieskaktus<br />

Psidium guajava Guava Koejawel<br />

Ricinus communis Castor-oil plant Kasterolieplant<br />

Xanthium strumarium Large cocklebur Kankerroos<br />

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