| INTRODUCTION This report covers the time
period from 1st October 2009 until 31st
December 2009. During this time, we have invested over 1 120 man
hours in vegetation and animal population dynamics surveys. These
are discussed herein.
The amount of work completed
is directly proportionate to the availability of resources. Funds
and manpower are solicited from international volunteers for this
purpose.
The data captured in these
reports is designed to advise management as well as demonstrate the
effectiveness of management action.
The information contained in
this report has been obtained through both casual observation as
well as basic monitoring techniques. Although the monitoring
techniques are not discussed in this report, they are available on
request.
In most cases,
sample sizes are acceptable and the majority of OWGR is
represented in the samples.
Contributors
to this report:
Robbie Prehn –
OWGR Committee & Pondoro Lodge
John Slabbert –
Transfrontier Africa: Research Assistant
Sean Hill –
Student: Game Ranch Management
Craig Spencer –
OWGR
Volunteer
assistance from:
-
Conservation Volunteers Australia
-
AVIVA Conservation Projects
-
Transfrontier Africa
Veld
condition:
-
Grass:
A basic survey to evaluate the
grass biomass at the end of the 2009 winter was
conducted in October 2009. The purpose of this
survey was to:
-
Gather base-line data with which
to compare the end of winter grazing with
consecutive years and show trends in response to
grazing pressure and rainfall.
-
To evaluate the accumulation of
moribund and therefore the potential fire-hazard.
This entailed selecting 31 separate monitoring sites (figure 1) that
would represent the reserve in two basic ways:
-
Water
availability: Those areas that
have well spaced water provided on a permanent basis, areas
that have wind pumped water only and the Cambridge 5 & 6
area that has a multitude of permanent water.
-
Rainfall and
soils: Covering enough of the
reserve to alleviate the potential bias of erratic rain-fall
and edaphically variable areas (different soils).

Figure 1. Spacial representation of the grass
survey plots in relation to water-points.
Results and interpretation:
§
In areas where water holes are
restricted to those pumped by wind, such as Impalabos East and West,
there was a markedly higher grass biomass at the end of winter.
Collectively these areas contributed 52.8% of the above-ground grass
biomass within OWGR.
§
Cambridge 5 & 6 and surrounding
areas contribute approximately 6.68% of the end of winter
above-ground grass biomass within the OWGR. Although the soils are
of a high quality, this low yield is attributed to the plethora of
water-points which allows grazers to concentrate in the area
throughout the year.
§
Interestingly the areas such as
Pondoro and surrounds that have permanent water, but well spaced,
contributes 33.21% of the above-ground grass biomass at the end of
winter.
§
The majority of above-ground
biomass of grass was attributed to the species Bothriochloae
radicans and Aristida congesta at this time of the year.
These are both increaser 2 species and have a very low forage value.
§
Bothriochloae radicans
is a sub-climax grass that forms tufts and is often found in clay
soils and at the base of termite mounds. Aristida congest,
however, is a pioneer grass and does not form tufts. It is one of
our more common grasses in OWGR.
§
Almost all grass biomass remaining
at the end of winter was found in refugia under fallen trees and at
the base of termite mounds (especially true for B. radicans).
§
The lack of grass biomass within 2
kilometers or the river is to be expected. It is perhaps a bit
distressing that the winter grazing yield at the end of the 2009
season was comparable with that along the Olifants River
(historically the only permanent water).
§
Areas that pump artificial water by
means of wind-pumps displayed a high grass biomass which is
attributed to a lower grazing pressure during wind-free (and
therefore water free) winter months.
§
It can also be said that areas such
as Pondoro which has well distributed water holes also enjoys a
higher grass biomass.
§
Soil conditions play a major role
in the capacity of an area to support grass biomass.

Figure 2. Chart
representing the percentage biomass in relation to the water point
categories.
It must be born in mind that
historical land-use practice will also contribute to results. IE. If
the area was subjected to intensive grazing or a fire regime, etc.

Figure 3. A
representation of the percentage biomass in relation to the areas
within the OWGR study area.
Results and interpretation:
§
In areas where water holes are
restricted to those pumped by wind, such as Impalabos East and West,
there was a markedly higher grass biomass at the end of winter.
Collectively these areas contributed 52.8% of the above-ground grass
biomass within OWGR.
§
Cambridge 5 & 6 and surrounding
areas contribute approximately 6.68% of the end of winter
above-ground grass biomass within the OWGR. Although the soils are
of a high quality, this low yield is attributed to the plethora of
water-points which allows grazers to concentrate in the area
throughout the year.
§
Interestingly the areas such as
Pondoro and surrounds that have permanent water, but well spaced,
contributes 33.21% of the above-ground grass biomass at the end of
winter.
§
The majority of above-ground
biomass of grass was attributed to the species Bothriochloae
radicans and Aristida congesta at this time of the year.
These are both increaser 2 species and have a very low forage value.
§
Bothriochloae radicans
is a sub-climax grass that forms tufts and is often found in clay
soils and at the base of termite mounds. Aristida congest,
however, is a pioneer grass and does not form tufts. It is one of
our more common grasses in OWGR.
§
Almost all grass biomass remaining
at the end of winter was found in refugia under fallen trees and at
the base of termite mounds (especially true for B. radicans).
§
The lack of grass biomass within 2
kilometers or the river is to be expected. It is perhaps a bit
distressing that the winter grazing yield at the end of the 2009
season was comparable with that along the Olifants River
(historically the only permanent water).
§
Areas that pump artificial water by
means of wind-pumps displayed a high grass biomass which is
attributed to a lower grazing pressure during wind-free (and
therefore water free) winter months.
§
It can also be said that areas such
as Pondoro which has well distributed water holes also enjoys a
higher grass biomass.
§
Soil conditions play a major role
in the capacity of an area to support grass biomass.
 Figure 2. Chart
representing the percentage biomass in relation to the water point
categories.
It must be born
in mind that historical land-use practice will also
contribute to results. IE. If the area was subjected to
intensive grazing or a fire regime, etc.
 Figure 3. A
representation of the percentage biomass in relation to the areas
within the OWGR study area.

Figure 4. Graph
showing the distribution of grass biomass within the study area.
It should also be born in
mind that the area received an above average rainfall for the season
and therefore these figures could represent a best case scenario. Table 1. Biomass per
hectare in relation to area and water sources.
|
area |
kg / ha |
|
water source |
kg/ha |
% biomass |
|
River Lodge |
54 |
Olifants river |
54 |
6.68% |
|
Impalabos East |
236.2857 |
wind pumps
(limited access to permanent) |
426.6857 |
52.80% |
|
Impalabos West |
190.4 |
|
Cambridge 5 + 6 |
59 |
multiple permanent |
59 |
7.30% |
|
Rome 4 - 6 |
268.4 |
limited permanent |
268.4 |
33.21% |
- As mentioned in the
previous report, many of our grasses appear to be shade-loving
and achieved a visibly higher biomass under bushes and shrubs or
fallen trees. Cleared areas and exposed areas show the lowest
above-ground grass biomass. This is attributed to both the
reduced grazing pressure as animals struggle to access grasses
growing in refuge under fallen trees, etc., as well as the micro
habitat that is created (shade and lower evaporation rates /
better water retention). It is therefore recommended that
further bush clearing by land-owners be discouraged until
further trials can be conducted to determine a best practice
model.
In conclusion, it
must be reiterated that in a semi-arid savanna such as ours, a
healthy fire would require as much 2 500 kg per hectare of moribund.
was observed and there is insufficient fuel to support a “healthy”
burn. It can therefore be established that we are well below the
threshold for successful burns as an ecological management tool in
the OWGR. This will be monitored over the years.
For the purposes of managing fires within our region, a flow-chart
has been designed to assist with this in the field. This is attached
as Appendix 1.
- Woody species:
The Visibility Index at the
end of winter 2009 was calculated in September and October and
had increased dramatically as expected.
In the absence of foliage on the woody species, visibility improved
from 19.48 metres from the road verges, up to 31.55 metres.
Table 2. Comparing Visibility Index between
the best and worst case scenario. Measured in metres.
|
|
summer |
winter |
|
minimum |
11.82 |
25.3 |
|
maximum |
22.79 |
35.39 |
|
average |
19.48 |
31.55 |
This was measured at the peak of the growth period (March) and again
in this reporting period just before the rains.
- Methodologies were
briefly discussed in the previous report.
A snap-shot of the influence
of elephants on our woody species has been compiled and is attached
as Appendix 2.
Water
Points
A map showing the
significant water points and their recharge methods is almost
complete. The Oxford and Cambridge 5 & 6 areas are still
under-represented and will be visited during the following reporting
period.
Water quantity and quality
surveys are still conducted on a monthly basis and showed that all
dams and pans were full. Several, including the Singwe Big Dam were
over-flowing following our good November rains and water quality was
good for all water-points.

Figure 5. Spacial
representation and recharge methods for water-holes captured to
date.
Subterranean water
The area that has the
potential to impact the sub-terrainian water the most is the
Cambridge 5 & 6 section of the Reserve. I base this on the multitude
of bore-holes within close proximity of each other.
Of the sites that we
continually monitor, the Singwe Bush-camp main site (under the
windmill) and the control site is no longer accessible as a result
of recent up-grading of these sites.
Despite the good early
rains, it would appear that the subterranean water is under pressure
and this will only increase as development of the Cambridge 5 & 6
holdings continues.
The results are as follows:

Figure 6. Bore holes
measured on the reserve compared with a 12 month average. Singwe
Main has been removed as the bore-hole has been capped.
All sites show a below
average value and this should be cause for caution. This is true for
sites that are not abstracted and this would indicate that there is
a correlation with the recharge rates and rain-fall to date and
therefore it cannot be assumed that the below average values are
related to over-abstraction. The Billy’s Lodge bore-hole that has
dropped approximately three metres, displayed the same pattern in
February 2009. By March it had recovered and perhaps this is related
to the occupancy of the properties during the summer season?
Although my data is little more than a snap-shot of two years, it
would appear that this trend is typical for this time of year.
Predator / Prey relationships
The ongoing data-capture
exercise that has been initiated in conjunction with Pondoro Lodge
to capture data relating to as any kills within the reserve,
continues.
§
Hyena activity has been observed in
the areas adjacent to Ukhozi and on Impalabos. Furthermore, calls
and sightings continue to increase in the area and Ezulwini Paradise
Camp has been visited on several occasions by a group of three
spotted hyena who appear comfortable with human activity.
§
Leopard sightings continue to
improved and the frequency of sightings have escalated as the
leopards become habituated to human activity. Sightings are still
frequent on Pondoro and surrounds as well as Cambridge 6 and Singwe
South.
§
Several black-backed jackals that
were suffering from Sarcoptic mange have recovered. However, it
would appear that several pups were lost in late December to this
parasite. Our Jackal populations appears stable.
§
Sightings of civets and other
smaller predators are frequent. Caracal remain elusive with
infrequent sightings and serval continue to be absent.
§
Sightings of the same adult female
cheetah and two sub-adults have been recorded frequently again
during this period and we were graced with the arrival of a collared
female cheetah which has been seen frequently
§
Lion pride dynamics are as per the
previous report and all lions have been accounted for during this
reporting period.
Table 3. Predator
acceptance frequencies in OWGR over the reporting period.
|
Predator |
Prey species |
N (sample size) |
% frequency |
|
Lion |
buffalo |
12 |
16% |
|
warthog |
8 |
10.66% |
|
kudu |
11 |
14.66% |
|
giraffe |
18 |
24% |
|
wildebeest |
8 |
9.33% |
|
waterbuck |
3 |
4.10% |
|
bushbuck |
1 |
1.33% |
|
zebra |
9 |
12% |
|
impala |
5 |
6.66% |
|
Leopard |
impala |
6 |
60% |
|
guineafowl |
1 |
10% |
|
grey duiker |
1 |
10% |
|
bushbuck |
1 |
10% |
|
wildebeest |
1 |
10% |
|
Cheetah |
impala |
3 |
75% |
|
steenbok |
1 |
25% |
Lion continue to favor buffalo as their chosen prey species and
although wildebeest make up a humble 9.33% of their kill rate, this
amounted to 88% of the wildebeest population according to the aerial
census. This is a shocking figure if the census results are a true
reflection of the animal numbers. However, our wildebeest herds that
we have under management number a total of 31 animals and this is
just a small
snap-shot. Irrespective, the acceptance
frequency may be low for wildebeest, but the following table will in
demonstrate the importance of seeing this in context with the
population size.
Table 4. Percentage of each species
population that was taken by predators in this reporting period.
Based on 2009 aerial census.
|
Prey species |
N (sample size) |
OWGR 2009 census figures |
% of population |
|
buffalo |
12 |
25 |
48% |
|
warthog |
8 |
26 |
30.76% |
|
kudu |
11 |
98 |
11.22% |
|
giraffe |
18 |
50 |
36% |
|
wildebeest |
8 |
19 |
88.88% |
|
waterbuck |
3 |
74 |
4% |
|
bushbuck |
2 |
3 |
75% |
|
zebra |
9 |
78 |
11.53% |
|
impala |
13 |
680 |
1.91% |
|
guineafowl |
1 |
N/A |
N/A |
|
steenbok |
1 |
1 |
100% |
This table is a poor representation of species
which demonstrate a stochastic distribution pattern and should be
seen as an indicator only. IE. If it was to be believed, then
predators caused the extinction of steenbuck in OWGR! One more bite
and the wildebeest will follow suite! This is not what we are trying
to demonstrate, but rather work towards a Catch-Per-Unit-Effort
concept for prey selection. This is one method of measuring this.
·
Note the value that the impala has
as a prey species for other large predators. Both leopards and
cheetah favour this species possibly due to the Catch Per Unit
Effort model.
§
Again, much of the lion activity
was concentrated on the Singwe and Cambridge 2, 3, 5, 6 & 7 areas
during this reporting period, with visits to Rome 1 to 9 and
Impalabos. Despite the York Pride spending a lot of its time in the
Western Sector, they still frequent the other sectors of the reserve
and territorial patrols by the two-male-coalition are observed from
time to time.
Table 5. Age and sex
class frequencies per prey species (this reporting period).
|
PREY DYNAMICS |
|
PREY SPECIES |
MALE |
FEMALE |
|
|
Lions |
ADULT |
SUB_ADULT |
JUV |
INFANT |
ADULT |
SUB-ADULT |
JUV |
INFANT |
UNKNOWN |
|
Buffalo |
13.30% |
8.30% |
|
|
25% |
|
|
|
50% |
|
Warthog |
|
|
|
|
14.00% |
|
|
14% |
71.00% |
|
Kudu |
22.00% |
|
|
|
22.00% |
11% |
|
|
44.00% |
|
Giraffe |
7.00% |
|
|
7.00% |
28% |
|
|
|
58.30% |
|
Wilderbeest |
28% |
|
|
|
14% |
|
|
|
57% |
|
Bushbuck |
|
|
|
|
|
|
|
|
100% |
|
Impala |
|
|
|
|
66% |
|
|
|
|
|
Waterbuck |
33% |
|
|
|
66% |
|
|
|
|
|
Leopard |
|
|
|
|
|
|
|
|
|
|
Impala |
33% |
|
|
|
|
|
|
|
66% |
|
guenifowl |
|
|
|
|
|
|
|
|
|
|
bushbuck |
100% |
|
|
|
|
|
|
|
|
|
wildebeest |
|
|
|
|
|
|
|
|
100% |
|
grey duiker |
|
|
|
|
|
|
|
|
100% |
|
Impala |
66% |
|
|
|
|
|
|
|
33% |
|
Cheetah |
|
|
|
|
|
|
|
|
|
|
impala |
25% |
|
|
|
25% |
|
|
|
50% |
|
steenbok |
|
|
|
|
|
|
|
|
100% |
Alien Vegetation:
Opuntia ficus-indica
(Prickly Pears) are still being tackled systematically in the area
and are logged using a GPS. A database of their location is kept and
plants treated with MSMA are re-visited to ensure that they have
been effectively treated. Land owners on Ezulwini, Impalabos East
and West have been pro-active in the eradication of these weeds. The
areas of Rome 1 to 4 have not been surveyed as yet.
 Figure 7. Prickly
Pears treated or identified for treatment during this reporting
period.
FOCAL SPECIES – INDICATORS AND KEY-STONE
SPECIES
1. AFRICAN ELEPHANTS:
1. Elephant movements, impacts on vegetation
and population dynamics:
Mega-herbivores
are our major landscape architects in the region and are
critical to the ecological processes of the savannah
biome. Elephants have a controversial impact on the
vegetation within the savannah biome and this is
monitored along with their movement patterns and herd
dynamics. This is a major focus of this project and we
have partnered with the Save the Elephant Foundation and
the Trans-boundary Elephant Research organisation for
this purpose.
§
During this reporting period, 17
elephant sightings were recorded between October and December, with
a noticeable absence of elephants for the past 24 days. The profile
of elephants frequenting the area remains as young bulls with the
odd breeding herd making an appearance. All sightings and documented
according to the prescribed data-capture regime of the Save the
Elephant Foundation. This includes several breeding herds and bulls.
This data is handed on a regular basis to Drs. Henley. Much data was
lost due to the lightening strike that destroyed our computer
equipment.
Table 6. An example of the field – data – capture
forms utilised for the elephant sightings.
|
Date |
6-Dec-09 |
|
Time |
1700 |
|
Location |
Pondoro (S 24.18436 / E 030.94137) |
|
Social structure |
Bulls |
|
Number in group |
4 |
|
Individual Elephant info |
Elephant ID 1 |
Elephant ID 2 |
|
Sex (bull/cow) |
Bull |
Bull |
|
Size (small/medium/large) |
Large |
Medium |
|
*Musth/Nonmusth |
BM |
0 |
|
Tameness index (1/2/3/4) |
3 |
2 |
|
Age estimate |
> 35 |
28 |
|
Sequence of animals |
|
|
|
Code |
LE |
RE |
Ft |
Tk |
LE |
RE |
Ft |
Tk |
|
Photo number |
|
|
|
|
|
|
|
|
|
Number of photos taken |
|
|
|
|
|
|
|
|
1.2 Elephant influence on
woody species:
The influence that elephants
have on the woody species within the reserve is an important issue
to understand. As a result, we have designed a monitoring protocol
to assess this on a fine scale.
§
This monitoring regime comprises
three transects that represent the vegetation communities of the
reserve as well as the influence that roads have in the movements of
elephants.
§
Plots are established in these
transects and woody species are examined for damage caused by
elephants.
§
Elephant related damage is
quantified and the tree/shrub’s response is also noted.
§
An acceptance frequency of target
species (Gadd, M. 1997) is employed to determine the preferred
target species of trees or shrubs.
Table 7. Example of field data capture
sheet employed to assess the fine-scale impacts of elephants on the
woody vegetation.
|
TREES VS ELPHANTS |
Date |
18-Nov-08 |
|
|
|
Transect start |
Height of tree |
Plant data |
|
Spp. |
1.5m-2.5m |
2.5m-4.5m |
>4.5 |
Multi stem |
Single stem |
Damage |
minor |
average |
major |
Bark strip |
Limb broken |
Up-rooted |
Dead |
Coppicing |
Healed |
Pathogens / Rot |
Browsing signs |
|
GPS - S24.09.360 E 30.56.917 |
|
Raintree |
x |
|
|
x |
|
x |
|
|
|
|
|
|
|
|
|
|
|
|
Raintree |
|
x |
|
x |
|
x |
|
|
|
|
|
x |
|
x |
x |
|
|
|
Weeping Wattle |
|
|
x |
x |
|
x |
|
|
|
|
|
x |
x |
|
|
x |
|
|
Raintree |
|
x |
|
|
x |
x |
|
|
|
x |
|
|
|
|
|
|
|
|
Knobthorne |
|
|
x |
|
x |
x |
|
|
|
|
x |
x |
x |
|
|
x |
|
|
Knobthorne |
|
|
x |
|
x |
x |
|
|
|
|
x |
|
|
x |
|
|
|
|
GPS - S24.09.407 E030.56.924 |
|
Bushwillow |
|
x |
|
|
x |
x |
|
|
|
|
|
x |
x |
|
|
x |
|
|
Knobthorne |
|
|
x |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Raintree |
x |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Shepphard's tree |
x |
|
|
x |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Russet Willow |
|
x |
|
x |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Magic Guarri |
|
x |
|
x |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Corkwood |
|
x |
|
|
x |
|
|
|
|
|
|
|
|
|
|
x |
|
|
Corkwood |
|
x |
|
|
|
|
|
|
|
|
|
|
|
|
|
x |
|
Table 8: The varying forms of damage to
three different height classes of trees with percentage of damage
caused.
|
Size |
Total trees |
Uprooted |
% |
BS |
% |
LB |
% |
Browse |
% |
|
<1.5m |
201 |
13 |
15.40% |
0 |
0.00% |
58 |
34.60% |
10 |
20.10% |
|
1.5-4.5m |
185 |
2 |
9.25% |
0 |
0.00% |
65 |
28.40% |
13 |
14.20% |
|
>4.5m |
115 |
2 |
5.75% |
7 |
16.4% |
66 |
74.20% |
12 |
9.50% |

Figure 8. New damage (caused by elephants) to trees vs old
damage.
§
Due to
the fact that the SAVANNA Project is in its infancy, much
base-line data-capture is required for the first few years
,
before we can start to draw comparisons.

Figure 9. Vegetation community
structure represented as percentage occurrence of target
species.
Our research has shown that the elephant
herds, and more specifically the bulls, seem to favor using
roads to access areas of the reserve. As a result of the
concentration on these roads, more trees are damaged in the
areas directly adjacent to the roads. The problem with this is
that the general public, managers and rangers travel the roads
and have therefore developed an opinion of the elephants and
their impact on the trees based on casual observations whilst
they traverse the internal roads.

Figure 10. A snap-shot from our data-set
indicating the significant increase in the damage to
trees caused by elephants along road verges.
2. WHITE AND BLACK
RHINOCEROS
Rhino are a high value
species and white rhino, being bulk grazers, are a good indicator of
grass biomass and habitat. There has been a new surge in the illegal
hunting of rhino on the sub-continent and as a result, we have begun
to compile a profile of each rhino that establishes itself in the
area.
For this purpose,
Photographic Identification has been initiated as well as the GPS
location of all dung-middens that could indicate a new territory.
Distribution maps are considered sensitive and will be distributed
on request.

Figure 11. An example
of white rhino sightings observed in the eastern sector. This
information is considered sensitive and details are available on
request.
|
Name: |
Craig Spencer |
|
Lodge/property: |
Impalabos East. Xikankanka Dam |
|
Date |
2/12/2009 |
|
Time |
1.50pm |
|
Location |
Olifants West Region. Balule Nature Reserve. S24,23128
E30,95689 |
|
Social structure |
lone |
|
Number in group |
single |
|
Individual Rhino info |
   
|
Left angle - horns |
Right angle - horns |
front - horns |
total animal |
|
Sex (bull/cow) |
Bull |
|
|
|
|
|
Size (small/medium/large) |
Large |
|
Tameness index (1/2/3/4) |
3 |
|
Age estimate |
Adult |
|
Name / ID No. |
Roger |
|
Notes: |
Pinkpatches on upper lip |
|
|
|
Figure 12. Example of a photo-identikit
for our rhinos.
This work is on-going and it is essential
that all rhino are captured on our data-base as a type of assets
register.

|
The
radio-telemetry is used on a daily basis to locate the
black rhino in the area. We have not seen any tracks or
picked up a signal since late in November. Last seen in
Rome 8, 8 and Ukhozi. There have been unsubstantiated
reports that a black rhino was seen in the Rome 2 area,
which would indicate that our trackers are not being
honest with us, and the radio telemetry is not
functional. For security reasons, this must be ve |
1.
BLUE WILDEBEEST:
| Blue wildebeest are also one of
our indicator species which are indicative of a
“healthy” tree / grass ratio within the savannah biome.
The blue wildebeest population in Balule has been on a
downward spiral for several years and it is essential
that we monitor this trend and advise accordingly |

Figure 14. The sudden drop in blue
wildebeest numbers. The trends are being monitored
against predator pressure as well as
vegetation dynamics (habitat structure).
|
For this to be
effective, we have begun to monitor recruitment rates
and mortalities in each age and sex group, as well as
herd dynamics and habitat preferences.

Figure 15. GIS model showing
the locations of blue wildebeest herds in relation
to water availability and
our vegetation survey sites.
As mentioned
earlier in this report, we have identified three herds
and three transient bulls as our focal individuals of
this species. This total 31 animals and is considered a
representative sample.
Incident
reports:
§
The fence alarm is
triggered from time to time and Wynand is quick to
respond at all times. No security threats have been
reported to date.
§
The first big rains
washed several big holes under the fence and these were
speedily repaired.
§
Animal mortalities: We
are aware of three sub-adult male impala and one adult
female waterbuck that died on Cambridge 1, Campfire and
Rome 9 respectively. The cause of death was unknown and
further investigation not possible on all but one case
as scavengers had devoured the carcass. The female
waterbuck appeared to have died of a cytotoxic bite to
the right back leg as there were signs of necrosis.
Interestingly a leopard was observed the same night
feeding on the carcass.
Anti
Poaching:
§
Since my last report,
OWGR has appointed an expert tracker on a permanent
basis. Derrick resides at the compound at the main
access gate and routinely patrols the boundary fence
every morning. Following his routine fence patrol, he
then patrols hot-spots that we have jointly
predetermined.
To date, Derrick has removed several small snares which
all seem old, from the drainages on Cambridge 2, 3 and 5
& 6.
§
A large cable-snare was
removed from Cambridge 3 after it was spotted by the
tracker and ranger from Naledi Lodge. A special thanks
to Team Naledi for their continued assistance and
vigilance. This snare was intended for large game and
was large and strong enough for buffalo, giraffe and
perhaps rhino.
§
Naledi Lodges also
kindly supplied much of the uniform items for Derrick
and continues to provide logistical support when
required.
Interesting sightings:
§
The group of three
ground hornbills are still seen on a frequent basis on
Rome 9.
§
Impala and wildebeest
calved well this year and their progress is being
monitored to determine recruitment rates.
Cambridge
2 & 3 roads:
The Cambridge 2
and 3 road network has been completed on schedule and
traversing by several lodges has begun. This has already
born fruit as the “eye’s and ears” of the rangers from
the various lodges have reported the snare mentioned
earlier and lion activity has been recorded, thereby
increasing our data-base of predator / pray statistics.
Other
On-Going data-capture and monitoring initiatives:
Last years 3rd
year conservation student passed well and has been
promoted to Research Technician. A further 3rd
year student from Tswane University of Technology, Sean
Hill, has been employed to assist with the veld
condition scores for this year.
CONCLUSION:
All the data
summarized in this report is available for scrutiny and
methodologies not discussed here are available for
further scrutiny. These are just snap-shots taken from a
larger data-set and should be seen as such.


In order to
stream-line our management decision making processes and
ensure consistency in this regard, I have proposed the
following flow-charts as discussion documents in this
regard:
This report
compiled by:
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