investigation into production and reproduction …
TRANSCRIPT
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2020
Published by
Department of Agriculture, Land Reform and Rural Development
Design and layout by:
Directorate: Grootfontein Agricultural Development Institute
Private Bag X529, Middelburg, 5900
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CONTENTS
Identification of genomic regions associated with body weight and reproduction in two South African sheep
breeds ....................................................................................................................................................................................... 1
Evaluation of maternal breeding values for early body weights as selection criteria in Dohne Merino sheep ........................ 6
Establishment of a reference population for future implementation of genomic breeding values for the South
African Merino sheep breed ................................................................................................................................................... 10
Genome-wide association study to identify genetic markers associated with resistance to Haemonchus contortus in
sheep ...................................................................................................................................................................................... 13
Measurement of morphometric traits and assessment of subjective traits determining body conformation at various
ages in Dohne Merino sheep .................................................................................................................................................. 16
Prediction of tail weight from tail measurements in Namaqua Afrikaner sheep .................................................................... 21
Description and comparison of different mating and kidding systems used in the South African Angora goat
industry .................................................................................................................................................................................. 25
Studies on the detection, control by vaccination and the genetics of Ovine Johne’s Disease ................................................ 30
Establishment of the South African biological reserve for small stock research and conservation ....................................... 33
Establishment and maintenance of live flocks of the endangered Namaqua Afrikaner sheep breed in South Africa ............ 35
Maintenance of two Merino flocks as resource flocks for research and reference flocks for a biological bank for
Merino sheep in South Africa ................................................................................................................................................ 39
Maintenance of an Afrino flock as resource for research and as reference flock for a biological bank for Afrino
sheep in South Africa ............................................................................................................................................................. 43
Blood and DNA bank for genomic research in sheep and goat breeds in South Africa ......................................................... 47
Satansbos monitoring and control .......................................................................................................................................... 53
Other Pasture Science projects ............................................................................................................................................... 55
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Preface
The Grootfontein Agricultural Development Institute (GADI) is situated near the town of Middelburg in the Eastern
Cape and the institution serves the small stock sector of the country. It hosts the Grootfontein College of Agriculture
and has the expertise to provide the highly sought-after education of its small stock focused curriculum. The College is
fully accredited as an institution of higher learning. In addition, the institute is a key role-player in sheep and goat
production research nationally and has built a knowledge base that supports the profitability and sustainability of the
small stock sector and enhances natural resource management in small stock producing areas. The research program is
strongly client-driven and is financially supported by the industry.
This report gives an account of the research activities and outputs of the institute. For monitoring and evaluation of
progress with the research and development (R&D) program, researchers are annually requested to submit
comprehensive progress reports on each individual R&D project by the end of July. For this, data collected to date in
each project are analysed and reported. For obvious reasons, the preliminary results reported in some progress reports
cannot be released, as they might be misleading or may be misinterpreted. Therefore, this research report only contains
abstracts from the comprehensive progress reports for the 2019-2020 reporting period. The publications mentioned in
the reports are available on the GADI website (http://gadi.agric.za/articles.php) or from the respective authors.
The key clients of the GADI program are farmers (commercial, small holder and subsistence), learners (students),
national and provincial departments of agriculture, agricultural industries, as well as district and local municipalities.
The interests of most land users are represented by the departments of agriculture (national and provincial), commodity
organisations, agribusiness, breeders’ associations and organised agriculture. As GADI’s R&D program is largely
driven by client needs, different stakeholders financially support many of the research projects. The stakeholders
provided approximately 77% of the operational cost of the GADI R&D program during 2019-2020. Financial support
during the reporting period was obtained from Cape Wools SA, Red Meat Research and Development SA and the
Thünen Institute (Germany). Financial support from different stakeholders to the GADI R&D program is administrated
through the Small Stock Research Trust.
Other stakeholders and research partners who contributed towards the GADI R&D program in the form of physical
execution of research projects are:
• Eastern Cape Department of Rural Development and Agrarian Reform (Cradock and Dohne Experimental
Stations)
• Northern Cape Department of Agriculture, Land Reform and Rural Development (Carnarvon, Karakul and
Koopmansfontein Experimental Stations)
• Western Cape Department of Agriculture (Elsenburg Directorate of Animal Sciences)
• 18 commercial farmers and their farm workers in five provinces
• BKB.
The COVID-19 pandemic that hit South Africa in March 2020 caused the President to declare a state of disaster in the
country. Different stages of lockdown were enforced, starting with a total lockdown at Level 5 from 27 March. This
was reduced to lockdown level 4 on 1 May and level 3 on 1 June. During levels 5 and 4, no research activities could
take place, while limited activities were resumed during level 3 since 1 June 2020. Therefore, some project activities
could not take place as stipulated in the project proposals. Different projects were affected to various degrees. This will
be discussed in each project abstract.
1
Identification of genomic regions associated with body weight and reproduction in two South
African sheep breeds
M.A. Snyman & S. Sűllwald
AIM AND OBJECTIVES
The aim of this project was to identify genomic regions associated with body weight and reproduction in two South
African sheep breeds.
The objectives of this project were to:
• Obtain blood samples of the identified animals from the GADI-Biobank
• Isolate DNA from the blood samples
• Genotype samples with the Illumina® Ovine SNP50 BeadChip
• Perform principal component analyses to identify clusters of genetically divergent animals in terms of
reproduction and growth within and among flocks
• Perform a genome-wide association study to identify genes associated with body weight and reproduction in the
three flocks
• Contribute genomic data to the South African reference sheep population data bank.
BACKGROUND
This project was done as an MSc study as part of project AP1/17/2: “Genome-wide association study to identify
possible genetic markers (SNPs) associated with reproduction and body weight in different sheep flocks”. This project
will lay the basis for a further in-depth genome-wide association study.
MATERIAL AND METHODS
Phenotypic data, pedigrees and genotypes available on animals of the Afrino flock at the Carnarvon Experimental
Station, the fine wool Merino stud at Cradock Experimental Station and the Merino stud at Grootfontein Agricultural
Development Institute (GADI) were used in this study. These resources were obtained from the GADI-Biobank.
Phenotypic traits included in the study were body weight recorded at selection age at 14 months of age (BW), number
of lambs born (NLB), number of lambs weaned (NLW) and total weight of lamb weaned (TWW). For each flock,
animals with a range of low to high estimated breeding values (EBVs) for all traits were selected amongst the animals
with available genotypes in the GADI-Biobank. A total of 411 genotypes, comprising 152 Afrino, 129 Cradock Merino
and 130 Grootfontein Merino animals, were included.
The individual genomic datasets for each flock were updated with Oar v4.0 SNP Chimp that was downloaded from the
SNPchiMp v.3 database. Only five animals did not meet the quality standards and their genotypes were excluded from
further analyses. The total number of SNPs retained after quality control was 42117 for the Afrino, 46196 for the
Cradock Merino and 43655 for the Grootfontein Merino datasets. Admixture plots were used to indicate the population
structures that were based on the proportion of shared ancestral SNP genotypes. Principal Component Analyses (PCA)
were performed to investigate the genetic relatedness of individuals within and between the populations using the
merged dataset comprising all three flocks. For the genome-wide association study (GWAS) the Afrino, Cradock
Merino and Grootfontein Merino datasets were analysed separately for each flock and each trait, using the software
Efficient Mixed Model Association Expedited (EMMAX). Results from the association analyses were visualised by
creating manhattan plots in R-studio. From the manhattan plots SNP markers associated with reproduction and body
weight were identified. Genes associated with these SNPs were identified and further investigated.
RESULTS
Genetic relatedness within and between populations
The relatedness within and between the three populations is illustrated by the PCA shown in Figure 1. All three
populations, namely the Afrino, Cradock Merino and Grootfontein Merino, cluster according to geographical region
and show flock structure. The Afrino population forms a tight cluster separate from the two Merino populations. The
two Merino populations, Cradock and Grootfontein, show two clusters based on their respective populations and
geographical origin, with some overlapping of individuals between the two populations. This genetic relatedness
between the two Merino populations could be attributed to the use of the same rams in these two populations.
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-0.050
0.000
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0.100
-0.100 -0.050 0.000 0.050 0.100
Pri
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Co
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Principal Component 1
Afrino
Cradock Merino
Grootfontein Merino
Figure 1. Genetic relationships among the 406 sheep for the first and second principal components
Admixture analysis performed on the merged dataset indicated that the lowest cross-validation error was at K=3.
Therefore, the population substructure for the three populations is illustrated in Figure 2 for K=3. From Figure 2 it is
clear that the two sheep breeds have their own distinct ancestral backgrounds and this confirms the results shown in the
PCA plot in Figure 1. It is also evident that the Cradock Merino population shows some admixture with the
Grootfontein Merino population, due to the sharing of sires.
Afrino Cradock Merino Grootfontein Merino
Figure 2. Population structure plot (K=3) of the three sheep populations
SNPs and genes in association with body weight and the reproductive traits
For the Afrino population three suggestive SNPs were identified with a putative association with BW. Two SNPs were
situated on chromosome three (s10640.1, OAR3_195631696.1) and one on chromosome fourteen
(OAR14_56900862.1). No suggestive SNPs were identified in the Cradock Merino population, while one suggestive
SNP (OAR9_64654880.1) in association with BW was identified for the Grootfontein Merino population on
chromosome nine.
Two suggestive SNPs located on chromosome one (s27280.1; OAR1_10554666.1) were identified for the Cradock
Merino population for NLB. No suggestive SNPs were identified for either the Afrino population or the Grootfontein
Merino population.
Again, two suggestive SNPs associated with NLW were identified in the Cradock Merino population. These two SNPs
were situated on chromosomes one and four respectively. For the Grootfontein Merino population there was only one
suggestive SNP (OAR2_150119548.1) identified on chromosome two in putative association with NLW. No
suggestive SNPs were identified in the Afrino population.
Only one suggestive SNP (OAR7_76295917.1) with a putative association with TWW was identified on chromosome
seven in the Afrino flock. In the Cradock Merino flock one suggestive SNP located on chromosome one (s27280.1)
was identified that had a putative association with TWW. No suggestive SNPs were identified in the Grootfontein
Merino population.
Some of the SNPs were associated with all three reproductive traits. In the Afrino population SNP OAR7_76295917.1
was above the suggestive line for TWW and approached the suggestive lines for both NLB and NLW. In the Cradock
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Merino population two SNPs (s27280.1 and OAR4_28838482_X.1) were associated with more than one trait. SNP
marker s27280.1 was found to be suggestive for all three reproductive traits namely NLB, NLW and TWW, while
OAR4_28838482_X.1) was suggestive for NLW and approached the suggestive line for TWW.
Possible genes associated with the identified suggestive SNP markers were obtained from the Ensembl database. Seven
of the putative SNPs were associated with thirteen genes. The SNPs, their positions and associated genes are
summarised in Table 1. Of the four suggestive SNPs identified in the Afrino population, only two were associated with
previously annotated genes. In total, six genes were associated with these two SNP markers in the Afrino population.
Each of the three suggestive SNPs identified in the Cradock Merino population was associated with a gene. The same
applied for the Grootfontein Merino flock, where both identified suggestive SNPs were in association with genes.
Table 1. Suggestive SNPs identified in the populations with their associated genes
SNP OAR SNP
Position Flock
Reference
SNP name Trait Gene
s10640.1 3 183769978 Afrino rs412166010 BW -
OAR3_195631696.1 3 181430556 Afrino rs404340346 BW -
OAR7_76295917.1 7 69590358 Afrino rs411617467 TWW SIX6
C14orf39
OAR14_56900862.1 14 53769443 Afrino rs420470779 BW
BSPH1
LIG1
CABP5
ELSPBP1
s27280.1 1 11378621 Cradock
Merino rs415733675
NLB
NLW
TWW
GRIK3
OAR1_10554666.1 1 10806824 Cradock
Merino rs430430819 NLB MAP7D1
OAR4_28838482_X.1 4 27440899 Cradock
Merino rs430227025 NLW HDAC9
OAR2_150119548.1 2 141206227 Grootfontein
Merino rs429823566 NLW
XIRP2
ENSOARG00000022371
OAR9_64654880.1 9 61385044 Grootfontein
Merino rs398224229 BW
TRPS1
ENSOARG00000026539
DISCUSSION
Nine suggestive SNPs were identified in the GWAS performed on the three sheep populations. Of these, four SNPs on
OAR3, OAR9 and OAR14 were associated with body weight, and five SNPs found on OAR1, OAR2, OAR4 and
OAR7 were associated with the reproductive traits. Two of the four suggestive SNPs associated with body weight in
the current study were situated close to or with-in candidate genes, namely one (OAR9_64654880.1) on OAR 9
identified in the Grootfontein Merino sheep, and another (OAR14_56900862.1) on OAR 14 identified in the Afrino
population. The SNP OAR9_64654880.1 was situated within the TRPS1 gene and in close proximity of the
ENSOARG00000026539 gene, while SNP OAR14_56900862.1 was close to the genes BSPH1, LIG1, CABP5 and
ELSPBP1.
TRPS1 is a transcriptional repressor protein that influences GATA binding. The gene is also a negative regulator of
RNA polymerase II transcription and involved in the development of the skeletal system. An association of TRPS1
with post weaning growth rate in sheep was reported. Several other studies reported the involvement of TRPS1 in
economically important traits such as mammary gland morphogenesis and development in dairy cattle, carcass weight
and eye muscle area in beef cattle and hair growth in cashmere goats. This gene should be further investigated in terms
of its role in body weight in sheep.
The gene ontology databases reported BSPH1 to be involved in spermatid development, more specifically in the
binding protein that binds sperm in vitro and promotes sperm capacitation. In a study on litter size in Finnsheep and
Texel sheep and their F1-crosses, the BSPH1 gene was expressed in both crosses. No previous literature provide
evidence that it is associated or involved with body weight or growth in sheep.
The LIG1 gene is primarily involved in DNA ligase activity and DNA/RNA repair and replication. A GWAS
investigated calf birth weight in Holstein cattle and identified LIG1 in the pooled SNPs that could possibly have an
association with body weight. In another study, LIG1 was also identified as a novel, possibly growth-related gene.
Both studies could not directly link the LIG1 gene to body weight or growth, but both reported the gene to be involved
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in the underlying mechanisms of growth. The current study adds to this body of evidence, and the gene should be
further investigated in terms of its role in body weight.
Literature reported that the ELSPBP1 gene is involved in the quality control mechanisms of epididymal maturation of
sperm and phosphorylcholine-binding activity during ejaculation. However, no literature supports the gene’s
involvement in body weight or growth.
From the five suggestive SNPs associated with the reproduction traits, two were in association with NLB (s27280.1
and OAR1_10554666.1), three with NLW (s27280.1, OAR2_150119548.1 and OAR4_28838482_X.1) and two with
TWW (s27280.1 and OAR7_76295917.1).
SNP s27280.1 that was identified in the Cradock Merino is of most interest as it was associated with all three
reproductive traits. This specific SNP is in close proximity to the GRIK3 gene, which is involved in nervous system
processes, regulation of membrane potential, synaptic transmissions and involved in the signalling pathway of the
glutamate receptor. Studies done on livestock found the GRIK3 gene to be associated with age at first egg in chickens
and with temperament and behavioural traits in cattle.
The OAR4_28838482_X.1 SNP identified in the Cradock population was linked to the HDAC9 gene. Gene-ontology
databases identified the HDAC9 gene as a histone deacetyl protein that plays an important role in regulating
transcription and cell cycle events like progression and development. The current study supports previous literature
that suggested that the gene could be involved in reproduction, fertility and weight or growth in vivo. Several studies
done on livestock associated the HDAC9 gene with skeletal muscle development and possibly with carcass and meat
traits. In cattle it was found that the gene was important in sperm quality in Holstein bulls to maintain spermatogonia
of stem cells during cell differentiation and ageing. Further investigation into the HDAC9 gene specifically for weight
and litter number is warranted.
The SNP OAR2_150119548.1 identified in the Grootfontein Merino population was associated with NLW and in close
proximity to the gene XIRP2. XIRP2 gene encodes a cytoskeletal protein that is part of the actin family, which is
involved in cellular and intra-cellular processes. A recent study revealed that XIRP2 gene is involved in type one
skeletal muscle fibres that are oxidative fibres that fatigue slowly. Further studies found the gene in pigs to be
associated with pork quality, meat quality in goats and in cattle to be associated with meat quality and feed efficiency.
In the current study the gene was in association with NLW, however no other studies linked the gene to reproduction
or prolificacy in livestock.
Regarding TWW, SNP OAR7_76295917.1 was identified in the Afrino population to be closely situated to two genes
namely SIX6 and C14orf39. The SIX6 gene is involved in eye development, transcription regulation, sensory system
and anatomical structure development. In previous literature the SIX6-Box has been directly linked to growth in cattle
and cashmere production in goat breeds. More recent studies on cattle and goats concur that the SIX6 gene is involved
in pituitary gland development, which influences downstream hormone production involved in puberty and growth of
animals. The studies conducted in cattle reported that the gene influences the expression and regulation of
gonadotropin-releasing hormone. This is an important growth hormone that affects puberty and reproduction in
livestock, and warrants further investigation.
It is interesting to note that two of the genes (BSPH1 and ELSPBP1) associated with body weight in the Afrino
population in fact are involved in the regulation of reproductive processes. Similarly, three of the genes associated with
reproduction (SIX6, XIRP2 and HDAC9) seem to also affect growth and carcass traits. In the case of SIX6 this is
understandable, as TWW comprised both the number of lambs as well as the weight of the lambs. Comparable results
have been reported for the LCORL gene. This gene encodes a transcription factor that appears to function in
spermatogenesis. Polymorphisms in this gene are associated with measures of skeletal frame size and adult height in
humans, growth and carcass traits in cattle and height in horses. The LCORL gene has also been identified in
association with growth and carcass traits and parasite resistance in sheep. The question could be asked if a similar
situation applied here or did continued simultaneous selection for body weight and reproduction in the flock, resulted
in genes that are located near to each other but affecting different traits, to become fixed?
PUBLICATIONS
None to date.
CONCLUDING REMARKS
In the current study GWAS was successfully used to identify regions of significance associated with body weight and
reproductive traits. Seven SNP markers were identified in the current study that were associated with known genes.
Gene ontology of the identified chromosomal regions identified six genes for body weight traits and seven genes
associated with reproduction traits in this study. Evidence in literature also links some of the identified genes to body
weight and reproduction. The genes (SNPs) LIG1 (OAR14_56900862.1), TRPS1 (OAR9_64654880.1), SIX6
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(OAR7_76295917.1), HDAC9 (OAR4_28838482_X.1) and XIRP2 (OAR2_150119548.1) show the most promise in
terms of candidate genes for improvement of reproduction and growth traits. Before recommendations regarding the
possible use of LIG1, TRPS1, HDAC9, SIX6 and XIRP2 in breeding plans could be made, their role in body weight and
growth traits in sheep should be clarified. For reproduction and fertility traits, the following genes require further
investigation: HDAC9 and SIX6. A more comprehensive GWAS incorporating more genotypes should be done to
verify these results.
ACKNOWLEDGEMENTS
The GADI-Biobank, the Eastern Cape Department of Rural Development and Agrarian Reform and the Northern Cape
Department of Agriculture, Land Reform and Rural Development are acknowledged for the use of their resources. This
work was supported by partial funding from Cape Wools South Africa.
6
Evaluation of maternal breeding values for early body weights as selection criteria in Dohne
Merino sheep
W.J. Olivier
AIM AND OBJECTIVES
The aim of this project is to evaluate maternal breeding values for early body weights as selection criteria in Dohne
Merino sheep.
The objectives of this project are to:
• Quantify the genetic relationships between growth and reproductive traits in the Grootfontein Dohne Merino stud
with regard to:
o Direct and maternal correlations of early body weights with body weight later in life
o Direct and maternal correlations of early body weight with reproductive traits (fertility, prolificacy, lamb
survival and weight of lamb weaned)
o Direct and maternal correlations of early body weights with fleece traits
• Define the most suitable selection criteria regarding maternal breeding values for early growth traits from the
results of the above-mentioned analyses
• Implement selection based on these criteria in the Grootfontein Dohne Merino stud
• Monitor genetic progress of the flock in growth, fleece traits and reproductive performance.
BACKGROUND
The data collected on the Grootfontein Dohne Merino stud to date will be used to determine the most efficient way of
including maternal breeding values for early growth traits in the selection program for this stud. Direct and maternal
genetic correlations among body weights at various ages and reproduction will be estimated. The selection strategy
will then be evaluated at the hand of direct and genetic trends in body weight, direct trends in reproduction, as well as
trends in fleece traits. This stud and the data recorded on the animals also form an integral part of the GADI-Biobank
since 2009. Phenotypes and genotypes recorded will be used for future genome-wide association studies and estimation
of genomic estimated breeding values.
Currently, the stud also forms part of the following research projects:
• AP1/19: Evaluation of maternal breeding values for early body weights as selection criteria in Dohne Merino
sheep
• AP1/17/1: Quantification of the genetic relationship between reproduction and body weight in different sheep
flocks
• AP1/17/2: Genome-wide association study to identify possible genetic markers (SNPs) associated with
reproduction and body weight in different sheep flocks
• AP2/21: Genome-wide association study to identify genetic markers associated with resistance to Haemonchus
contortus in sheep
• AP2/22: Measurement of morphometric traits and assessment of subjective traits determining body conformation
at various ages in Dohne Merino sheep
• AP10/3/6: Maintenance of a biological bank for Dohne Merino sheep in South Africa.
MATERIALS AND METHODS
The Grootfontein Dohne Merino stud (GDM) consists of 406 ewes. During March 2019 these ewes were mated to 12
rams from the stud and a ram from the Wauldby Dohne Merino stud. The rams were selected according to the selection
objectives of the project. The Wauldby ram was selected on its estimated breeding value for worm resistance and will
create a genetic linkage between these two studs.
The ewes were managed as one flock on the veld. Individual mating was practiced with a ram being mated to
approximately 31 ewes in small paddocks. The ewes were kept in individual pens during lambing for a ten-day period
and then kept for a maximum of two weeks in the kraals in Blikkiesdorp.
The PROC GLM procedure of SAS (2017) was used for statistical analysis. The fixed effects included in the analysis
of the production traits of the 2018-born lambs were sex, rearing status, age of the dam and age of the animal as a
covariable. In the analysis of the birth coat score and birth weight of the 2019 progeny, the age of the dam, rearing
status and sex were included as fixed effects, while age of the progeny was also included as a covariable for the
analysis of body weight at 42 days of age, weaning weight and 6-month body weight. Age of the ewe was included in
the model as a fixed effect for total weight of lamb weaned, the wool characteristics and body weight for the adult
ewes.
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RESULTS AND DISCUSSION
2018-Born progeny
The body weights and testis size recorded for the 2018 progeny are summarised in Table 1. The wool production data
at the age of 13 months are summarised in Table 2 and the subjectively assessed wool and conformation traits are
summarised in Table 3. The low clean yield of the rams (Table 2) compared to the ewes can most probably be ascribed
to the poor veld conditions during 2019. The ram lambs were kept in camps with a much poorer veld condition and a
higher dust content, especially around the feeding troughs.
Table 1. Birth coat score, body weights and testis measurements (± s.e.) of the lambs born in 2018
Trait Ram lambs Ewe Lambs
Birth coat score 1.0 ± 0.1 1.0 ± 0.1
Birth weight (kg) 5.4 ± 0.1 5.1 ± 0.1
42-day body weight (kg) 19.1 ± 0.2 18.3 ± 0.2
100-day weaning weight (kg) 28.7 ± 0.6 27.3 ± 0.6
6-month body weight (kg) 43.0 ± 0.8 37.2 ± 0.8
8-month body weight (kg) 44.2 ± 0.8 39.2 ± 0.8
12-month body weight (kg) 62.8 ± 1.0 44.9 ± 0.9
Testis circumference (cm) 31.9 ± 1.8
Testis length (cm) 16.5 ± 1.1
Table 2. Wool production data (± s.e.) of the 2018-born lambs at selection age (13 months)
Trait Ram lambs Ewe Lambs
Greasy wool (kg) 5.9 ± 0.1 3.2 ± 0.1
Clean wool (kg) 3.2 ± 0.1 2.4 ± 0.1
Clean yield (%) 54.7 ± 1.0 74.1 ± 1.0
Staple length (mm) 102.1 ± 1.8 91.8 ± 1.7
Fibre diameter (µm) 17.7 ± 0.2 17.1 ± 0.2
Crimps / 25 mm 12.4 ± 0.3 13.3 ± 0.3
Duerden 86.9 ± 1.3 86.2 ± 1.3
Standard deviation of fibre diameter (µm) 3.1 ± 0.1 3.2 ± 0.1
Coefficient of variation of fibre diameter (%) 17.4 ± 0.4 18.6 ± 0.3
Comfort factor (%) 99.7 ± 0.0 99.7 ± 0.0
Staple strength (N/Ktex) 42.8 ± 1.5 46.7 ± 1.5
Table 3. Subjectively assessed wool and conformation data (± s.e.) of the 2018-born lambs at 13 months of age
Trait Ram lambs Ewe Lambs
Wool quality 28.8 ± 0.7 29.3 ± 0.7
Creeping belly 21.6 ± 0.4 22.7 ± 0.4
Colour of the wool 32.2 ± 0.5 33.9 ± 0.5
Pigmentation 21.2 ± 1.3 35.4 ± 1.3
Wool score 5.2 ± 0.2 5.8 ± 0.2
Conformation score 28.7 ± 1.1 28.9 ± 1.1
2019-Born progeny
The reproduction data obtained from the 2019 breeding season are summarised in Table 4 and the body weights
recorded for the 2019 progeny are summarised in Table 5. It is evident from Table 4 that the ewes had a high
reproduction rate despite the very dry and poor veld conditions.
8
Table 4. Reproduction data (± s.e.) of the adult ewe flock in 2019
Trait Ewe flock
Number of ewes mated 406
Conception rate (%) 89.9
Lambing percentage (number of lambs born alive/number of ewes mated) 141.6
Weaning percentage (number of lambs alive at weaning/number of ewes mated) 124.4
Mortality of lambs:
Died between birth and 42 days (%) 8.7
Died between 42 days and weaning (%) 3.5
Died between birth and weaning (%) 12.2
Total weight of lamb weaned per ewe (kg)
Maiden ewes 22.7 ± 2.1
Adult ewes 31.4 ± 0.9
Table 5. Birth coat score and body weights (± s.e.) of the lambs born in 2019
Trait Ram lambs Ewe Lambs
Birth coat score 1.0 ± 0.1 1.0 ± 0.1
Birth weight (kg) 4.8 ± 0.1 4.5 ± 0.1
42-day body weight (kg) 16.6 ± 0.4 16.4 ± 0.4
100-day weaning weight (kg) 24.5 ± 0.9 23.7 ± 0.9
6-month body weight (kg) 34.4 ± 1.1 32.9 ± 1.1
Production of adult ewes
The production data of the adult ewes are summarised in Table 6.
Table 6. Production data (± s.e.) of the 2019 adult ewe flock
Trait Ewe flock
Body weight at mating (kg) 71.2 ± 1.2
Greasy wool (kg) 4.0 ± 0.3
Clean yield (%) 66.8 ± 1.4
Clean wool (kg) 2.7 ± 0.4
Fibre diameter (µm) 18.2 ± 0.6
Staple length (mm) 86.6 ± 1.2
Standard deviation of fibre diameter (µm) 2.9 ± 0.4
Coefficient of variation of fibre diameter (%) 16.0 ± 0.8
Comfort factor (%) 99.7 ± 0.7
Crimps per 25 mm 12.2 ± 0.5
Duerden 89.3 ± 1.5
Staple strength (N/Ktex) 40.6 ± 1.2
PUBLICATIONS
The following papers have been published to date on research done on this flock:
Herselman, M.J. & Olivier, W.J., 2006. Determining the relationship between staple strength and production and
subjectively assessed wool traits. Proceedings of the 42nd Congress of the South African Society of Animal Science,
Bloemfontein, 3-6 April, 95.
Olivier, W.J., Herselman, M.J. & Van Heerden, M., 2010. Production norms of the Grootfontein Dohne Merino flock.
Grootfontein Agric 10(1), 55-66.
Olivier, W.J., 2016. The effect of culling lambs at weaning on estimated breeding values of performance traits at 15
months of age of a Dohne Merino stud. Grootfontein Agric 16(1), 42-47.
Olivier, W.J., Van Graan, A.C. & Van Heerden, M., 2017. Estimation of genetic parameters for body weight and body
dimension characteristics in a dual purpose sheep flock. Proceedings of the 50th Congress of the South African
Society of Animal Science, Port Elizabeth, 18-21 September.
Olivier, W.J. & Van Heerden, M., 2017. Estimation of genetic parameters for reproduction traits in a dual purpose
sheep flock. Proceedings of the 50th Congress of the South African Society of Animal Science, Port Elizabeth, 18-
21 September.
9
Dlamini, N.M., 2018. A case-control investigation to evaluate resistance to Haemonchus contortus in South African
Dohne Merino sheep. MSc thesis, University of Pretoria, Pretoria, South Africa.
Dlamini, N.M., Visser, C., Soma, P., Muchadeyi, F.C. & Snyman, M.A., 2018. Genetic diversity and flock clustering
of a South African Dohne Merino flock selected for resistance to Haemonchus contortus. Proceedings of the 11th
World Congress on Genetics Applied to Livestock Production, Auckland, New Zealand, 12-16 February.
Dlamini, N.M., Visser, C., Snyman, M.A., Soma, P. & Muchadeyi, F.C., 2019. Genomic evaluation of resistance to
Haemonchus contortus in a South African Dohne Merino flock. Small Ruminant Research 175, 117-125.
(https://doi.org/10.1016/j.smallrumres.2019.04.020).
Olivier, W.J., Mashinini, I.D.M. & Van Heerden, M., 2019. Quantification of the relationship among reproduction
traits and body weight measured at various ages in a dual purpose sheep breed. Proceedings of the 51st Congress of
the South African Society of Animal Science, Bloemfontein, 10-12 June.
Olivier, W.J. & Van Heerden, M., 2019. Quantification of the relationship among body weight measured at various
ages in a dual purpose sheep breed. Proceedings of the 51st Congress of the South African Society of Animal
Science, Bloemfontein, 10-12 June.
Snyman, M.A., Dlamini, N.M., Visser, C., Muchadeyi, F.C. & Soma, P., 2019. Genetic variation in resistance to
Haemonchus contortus in the Wauldby and Grootfontein Dohne Merino flocks. Grootfontein Agric 19(1), 20-30.
CONCLUDING REMARKS
The project is running according to the project proposal.
ACKNOWLEDGEMENTS
The GADI and Small Stock Research Trust employees are acknowledged for their contribution to this project through
the maintenance of the animals and the collection of the data.
10
Establishment of a reference population for future implementation of genomic breeding
values for the South African Merino sheep breed
M.A. Snyman
AIM AND OBJECTIVES
The aim of this project is to establish a reference population for the South African Merino sheep breed, which will be
used for the implementation of genomic breeding values in the industry.
The objectives of the project are to:
• Identify suitable research flocks to participate in the reference population for the South African Merino sheep
breed and maintain these flocks
• Establish genetic links between these research flocks and industry flocks
• Identify suitable industry flocks to participate in the reference population for the South African Merino sheep
breed
• Collect blood samples and record required pedigree and phenotypic data from the participating flocks
• Identify high impact sires among other flocks and collect blood samples of these sires
• Genotype animals with the Illumina® Ovine SNP50 BeadChip
• Estimate genomic breeding values for the South African Merino breed
• Evaluate the available Illumina® Ovine SNP50 BeadChip for South African sheep breeds.
BACKGROUND
This project was initiated in 2013 with the main objective to establish a reference population for the Merino sheep
breed, which will ultimately be used for the implementation of genomic breeding values (GEBV) in the industry. This
is a collaborative project between all role players in the sheep industry. Scientists and technicians from GADI,
Elsenburg Directorate of Animal Sciences (EDAS), the University of Stellenbosch, the University of Pretoria and
Studbook SA are directly involved with data collection, capturing, processing and analyses, as well as blood collection
and processing. Due to logistic reasons, the project is divided into two production areas, with GADI and EDAS the
main centres for each area respectively.
MATERIALS AND METHODS
Progress in all objectives of the project is satisfactory. Research flocks, as well as industry flocks, form part of the
reference population.
The following Merino research flocks are included in the reference population:
• Cradock fine wool Merino stud (220 ewes)
• Grootfontein Merino stud (220 ewes)
• Elsenburg Merino reproduction lines (240 ewes)
• Tygerhoek Merino clean fleece selection line (40 ewes)
• Tygerhoek Merino fine wool line (200 ewes)
• Langgewens Merino flock (90 ewes).
The following four Merino studs with good links to the industry and complete phenotypic records are also part of the
reference population:
• Mr Eric Naude (Leopardsvlei, Middelburg; 1000 ewes)
• Mr Geoff Kingwill (Grand View, Murraysburg; 450 ewes)
• Mr Dirkie Uys (Komarsekraal, Bredasdorp; 600 ewes)
• Mr Johan Kotze (Korhaansrug, Moorreesburg; 500 ewes).
Blood sample, pedigree and phenotypic data collection
Blood collection during this reporting period could not take place as usual. Firstly, due to two broken freezers, there
was not enough freezer space to do the collections as usual. The freezers were repaired at the end of February 2020,
using surplus funds from other units at GADI. Therefore, blood samples were only collected from the 2019-born
Grootfontein Dohne Merino, Carnarvon Afrino, Carnarvon Namaqua Afrikaner and the La Rochelle Meatmaster lambs
before the COVID-19 outbreak, after which the lockdown prevented any further travelling for blood collections. Blood
samples from the other participating flocks will be collected as soon as possible. The number of Merino and other wool
sheep blood samples stored to date in the GADI-Biobank and EDAS-Biobank are given in Table 1.
All phenotypic data recorded have been entered into the respective databases.
11
Table 1. Number of Merino and other wool sheep blood samples in the GADI-Biobank and EDAS-Biobank
Breed Number of animals
GADI-Biobank
Merino - Cradock 4151
Merino - GADI 2793
Merino - E. Naude 5037
Merino - G. Kingwill 3069
Afrino 3701
Dohne Merino - Dohne ADI 1502
Dohne Merino - GADI 4684
Dohne Merino - Wauldby 1986
Total 26923
EDAS-Biobank
Merino - Tygerhoek 2277
Merino - Elsenburg 1184
Merino and Dohne Merino - Langgewens 783
Dormer - Elsenburg 235
SA Mutton Merino - Elsenburg 111
All breeds - Nortier 641
Population genetics study 876
Merino - D. Uys 1773
Merino - J. Kotze 985
Total 8865
Grand total 35788
Genotypes
Merino samples genotyped to date with the OvineSNP50 chip are summarised in Table 2.
Table 2. Merino samples already genotyped
Flock Number of
animals Year Genotyped at Funded by
Cradock fine wool Merino stud 48 2013 Geneseek Cape Wools
Cradock fine wool Merino stud 5 2016 ARC-BT a ARC
Cradock fine wool Merino stud 80 2018 ARC-BT Cape Wools
Cradock fine wool Merino stud 239 2019 Geneseek WCATb
Grootfontein Merino stud 37 2013 Geneseek Cape Wools
Grootfontein Merino stud 11 2016 ARC-BT ARC
Grootfontein Merino stud 80 2018 ARC-BT Cape Wools
Grootfontein Merino stud 257 2019 Geneseek WCAT
Geoff Kingwill 12 2016 ARC-BT ARC
Geoff Kingwill 6 2016 Geneseek Cape Wools
Geoff Kingwill 127 2019 Geneseek WCAT
Eric Naudé 22 2016 ARC-BT ARC
Eric Naudé 11 2016 Geneseek Cape Wools
Eric Naudé 484 2019 Geneseek WCAT
Elsenburg Hi-Lo Merino flock 91 2011 Geneseek THRIP
Elsenburg Hi-Lo Merino flock 408 2018 Geneseek WCAT
Langgewens Merino flock 24 2018 Geneseek WCAT
Industry sires 25 2016 Geneseek Cape Wools
Total 1967
a ARC-Biotechnology Platform, Onderstepoort b Western Cape Agricultural Trust. Funding for these genotypes was obtained from different funders, including Cape
Wools SA, Red Meat Research and Development SA (RMRD-SA), the Western Cape Agricultural Trust (WCAT), the
National Research Foundation through their Technology and Human Resources for Industry Program (THRIP) and
Research and Technology Fund (RTF) initiatives.
12
Identification of high impact sires
Merino SA has agreed to fund blood sample collection of a further 14 high impact sires in the industry for inclusion in
the reference population. Blood samples of these sires will be collected by officials from either GADI or EDAS,
depending on the locality of the specific sires.
Estimation of genomic breeding values (GEBV)
A PhD project “Development of systems for estimating genomic breeding values in South African wool sheep” is
currently underway. The student, Mr Nelius Nel is studying under Prof Schalk Cloete at the Stellenbosch University
(SU). Available genotyped Merino samples are being used in this study.
Furthermore, during a meeting of the Ovine genomics task team (Representatives from EDAS, GADI, University of
Pretoria, Stellenbosch University, University of the Free State, SA Studbook) on Tuesday 11 February 2020, a decision
was taken to do a preliminary GEBV analysis for the SA Merino breed incorporating the 1900 available genotypes of
the Merino reference population (Table 2 - the different Merino research flocks and the two industry flocks). During
this exercise, various aspects that still need clarification will also be investigated. The available genotypes will be
incorporated into the relationship matrix in a single step approach into the National BLUP evaluation. The phenotypic
data of the two industry studs of Mr Eric Naude and Mr Geoff Kingwill, as well as the Grootfontein and Cradock
Merino studs, are already part of the National BLUP evaluation and will be incorporated in the analysis. The other two
industry stud animals will be genotyped during 2020 and will then be included in the GEBV analysis. The phenotypic
data of the Elsenburg flocks will be incorporated into the national database for future GEBV analysis.
PUBLICATIONS
Another objective of this project was to evaluate if the available Illumina® Ovine SNP50 BeadChip could be used for
South African sheep breeds. Results indicated that the chip would yield accurate results for the Merino and other white
woolled breeds. The following articles were published on these results:
Sandenbergh, L., Cloete, S.W.P., Roodt-Wilding, R., Snyman, M.A. & Bester-van der Merwe, A.E., 2015. Genetic
diversity and population structure of four South African breeds. Proceedings of the Association for the
Advancement of Animal Breeding and Genetics 21, 294-297.
http://www.aaabg.org/aaabghome/proceedings21.php.
Sandenbergh, L., Cloete, S.W.P., Roodt-Wilding, R., Snyman, M.A. & Bester-van der Merwe, A.E., 2016. Evaluation
of the OvineSNP50 chip for use in four South African sheep breeds. South African Journal of Animal Science 46,
89-93.
Sandenbergh, L., Gore, K., Van der Werf, J.H.J., Olivier, J.J. & Cloete, S.W.P., 2016. Use of an Australian reference
population to impute genotypes of South African sheep. Proceedings 49th Congress of the South African Society for
Animal Science. Stellenbosch, 3-6 July.
Other publications
Sandenbergh, L. & Cloete, S., 2017. Genomics: what it means for the future of sheep breeding. Wool Farmer 4(6), 84-
87.
Cloete, S.W.P., Sandenbergh, L., Olivier, J.J., Van der Werf, J.H.J., Snyman, M.A., Scholtz, A.J., Cloete, J.J.E.,
Hoffman, L.C., Van Marle-Köster, E., Visser, C., Van Wyk, J.B. & Dzama, K., 2017. Selection for hard-to-
measure traits in the national sheep flock: recent progress and the way forward. Proceedings of the 50th Congress of
the South African Society of Animal Science, Port Elizabeth, 18-21 September.
CONCLUDING REMARKS
Progress in all objectives of the project is satisfactory.
ACKNOWLEDGEMENTS
The following people / institutions are acknowledged for their contribution to this project:
• Technicians at experimental stations for collection of data
• Participating breeders for their inputs
• Cape Wools SA, Red Meat Research and Development SA, Western Cape Agricultural Trust, Agricultural
Research Council, National Research Foundation through THRIP for funding of the project.
13
Genome-wide association study to identify genetic markers associated with resistance to
Haemonchus contortus in sheep
M.A. Snyman
AIM AND OBJECTIVES
The aim of this project is to identify possible genetic markers associated with resistance to Haemonchus contortus in
South African sheep, which could be incorporated into the selection plan.
This project comprises several phases. The first phase of the project is the data collection and selection phase and is
carried out on a farm in the Stutterheim district, known for its major H. contortus anthelmintic resistance problem,
under high natural internal parasite challenge. The objectives of the first phase are to:
• Annually record faecal egg counts (FEC), Famacha© score (FAM), body condition score (BCS) and body weight
of all September-born lambs every 14 days from weaning in January until the end of June
• Annually select ram and ewe lambs with a high degree of resistance / resilience to H. contortus infestation for use
in a selected line, in which the emphasis will be improved resistance to H. contortus
• Monitor selection progress with regard to resistance / resilience in the selected line
• Ascertain if sheep selected for resistance / resilience on this farm will exhibit similar resistance / resilience on
other farms under similar conditions and also under different climatic and nutritional conditions.
The second phase of the project comprises the protocol development and is carried out simultaneously with the first
phase. The objectives of this phase include:
• Annual data evaluation and analyses to determine the most suitable selection criteria for resistance / resilience
• Estimation of genetic parameters for resistance / resilience to H. contortus in South African sheep
• Calculation of selection indices and estimation of best linear unbiased predictors (BLUP-EBV) for resistance /
resilience
• Develop protocols for selection for resistant sheep to be applied on this and other South African sheep farms after
sufficient data have been collected.
The third phase of the project includes several genomic studies. The objectives of these studies are to:
• Select suitable resistant and susceptible animals for genotyping
• Genotype animals with the Illumina® Ovine SNP50 BeadChip
• Determine genetic variation in the flock
• Estimate population parameters for resistant and susceptible sheep
• Search for genetic markers associated with resistance to H. contortus within the flock through application of a
genome-wide association study
• Design a breeding plan for South African sheep incorporating genetic markers for resistance to H. contortus.
BACKGROUND
The farm Wauldby of Mr Robbie Blaine in the Stutterheim district has a well-documented history of heavy
H. contortus challenge and of H. contortus resistance to all five major anthelmintic groups on the market prior to 2011.
Several anthelmintic resistance trials have been done at Wauldby over the years. The severe anthelmintic resistance
problem on the farm has inadvertently resulted in selection of sheep over many years with a high degree of resistance /
resilience to internal parasites as drenching with anthelmintics has been largely ineffective. At the end of 2011, a
project aimed at selection for resistance to H. contortus was implemented, using the Dohne Merino stud of Mr Robbie
Blaine. The project was initiated by Dr Alan Fisher of the Queenstown Provincial Veterinary Laboratory (PVL). The
history of and recent selection practices followed in the Dohne Merino sheep flock at Wauldby makes it an ideal
resource for research into resistance to H. contortus.
MATERIALS AND METHODS
Phase 1: Data recording
Progress of the first phase of the project is satisfactory. A report on the results of the 2018-born lambs was sent to Mr
Robbie Blaine at the end of August 2019, for the purpose of selecting ewes and rams for the selected line. Data
collection of the 2019-born lambs continued from January 2020 onwards. This year, faecal egg counts (FEC) and BCS
were done in January, March and May, according to the developed protocols. Famacha© score (FAM) was still done
weekly. Body weight was recorded every month. As both Dr Alan Fisher and Dr Werner Wentzel are not affiliated
with the Queenstown PVL anymore, FEC were done at the Middelburg PVL. Dr Fisher, however, still assists with the
project.
14
Phase 2: Genetic parameters and protocol development
Data collected on the 2011- to 2016-born lambs have been analysed and the results published. A protocol for selection
for resistance has also been developed and published. See publications.
Evaluation of Wauldby sires selected for resistance / resilience on other farms
During the 2019 breeding season, one of the sires that has already been used in the Wauldby flock during 2018
(B16292), was obtained from Wauldby and used in the Grootfontein Dohne Merino stud to ascertain if sheep selected
for resistance / resilience on Wauldby will exhibit similar resistance / resilience on other farms under different climatic
and nutritional conditions. The breeding values for faecal egg count (EBV-FEC) were estimated for the Grootfontein
lambs born from 2014 until 2019. The Wauldby ram had the second best EBV-FEC of all sires used, which implies
that selection for resistance / resilience on Wauldby will be exhibited on other farms under different climatic and
nutritional conditions.
Sire B16292 was used again in the Grootfontein flock during the 2020 breeding season, while another farmer near
Thomas River, between Cathcart and Stutterheim, used sire B17144 during the 2020 mating season in his flock.
B17144 was already used during the 2019 and 2020 breeding seasons in the Wauldby flock.
Phase 3: Genomic study
The MSc study “A case-control investigation to evaluate resistance to Haemonchus contortus in South African Dohne
Merino sheep” was completed at the beginning of 2018 and the results published during 2018 and 2019.
Currently a more comprehensive genome-wide association study (GWAS) to search for genetic markers associated
with resistance to H. contortus is underway. Blood samples of 223 animals from the Wauldby flock (selected within
sire lines on the basis of EBV-FEC) and 66 animals from the Grootfontein Dohne Merino flock (selected within year
on high and low FEC) were genotyped with the Illumina® Ovine SNP50 BeadChip at the ARC Biotechnology
Platform. These genotypes, together with those previously genotyped for the MSc study, are used in the current GWAS
study.
Several significant SNPs associated with FEC, FAM and BCS were identified from the GWAS analyses. Many of
these SNPs have genes associated with them. Currently, the identified genes are further investigated as to their gene
ontology, function and any evidence from literature as to their involvement in parasite resistance.
PUBLICATIONS
The following have been published since the commencement of the project:
Fischer, A. & Snyman, M.A., 2014. Seleksie vir weerstand teen haarwurm in skape: Is dit prakties? Veeplaas. February
2014, 4, 80-83.
Fischer, A. & Snyman, M.A., 2014. Is dit prakties uitvoerbaar om te selekteer vir weerstand teen haarwurm in skape
onder Suid-Afrikaanse toestande? Dohne Merino Journal. December 2014, 25-37.
Fischer, A., Snyman, M.A. & Blaine, R., 2015. Practical breeding for resistance and resilience to Haemonchus
contortus in sheep. Vet News. July 2016, 5-7.
Botha, T., 2016. Wauldby se superskape troef haarwurm ál beter. Landbouweekblad.
14 October 2016, 68-71.
Burgess, M., 2016. Wauldby Dohne Merinos: on the veld for 68 years! Farmer’s Weekly.
15 January 2016, 52-55.
Snyman, M.A. & Fisher, A.D., 2017. Protocol for selection for resistance / resilience to Haemonchus contortus under
South African conditions. Proceedings of the 50th Congress of the South African Society of Animal Science, Port
Elizabeth, 18-21 September.
Snyman, M.A. & Fisher, A.D., 2017. Preliminary results of selection for resistance / resilience to Haemonchus
contortus in a South African Dohne Merino sheep flock. Proceedings of the 50th Congress of the South African
Society of Animal Science, Port Elizabeth, 18-21 September.
Snyman, M.A., Mashinini, I.D. & Fisher, A.D., 2017. Estimation of genetic parameters for resistance to Haemonchus
contortus in a South African Dohne Merino sheep flock. Proceedings of the 50th Congress of the South African
Society of Animal Science, Port Elizabeth, 18-21 September.
Fischer, A., 2017. Selecting Sheep for Resistance to Haemonchus contortus under summer rainfall South African
conditions – the first five years. Congress of the Rural Veterinary Association of South Africa.
Dlamini, N.M., 2018. A case-control investigation to evaluate resistance to Haemonchus contortus in South African
Dohne Merino sheep. MSc thesis, University of Pretoria, Pretoria, South Africa.
Dlamini, N.M., Visser, C., Soma, P., Muchadeyi, F.C. & Snyman, M.A., 2018. Genetic diversity and flock clustering
of a South African Dohne Merino flock selected for resistance to Haemonchus contortus. Proceedings of the 11th
World Congress on Genetics Applied to Livestock Production, Auckland, New Zealand, 12-16 February.
Snyman, M.A. & Fisher, A.D., 2018. Progress in selection for resistance to Haemonchus contortus in a South African
Dohne Merino flock. Grootfontein Agric 18(1), 1-19.
15
Snyman, M.A., Olivier, W.J. & Fisher, A.D., 2018. Genetic parameters for traits associated with resistance to
Haemonchus contortus in South African Dohne Merino sheep. Proceedings of the 11th World Congress on Genetics
Applied to Livestock Production, Auckland, New Zealand, 12-16 February, 288.
Dlamini, N.M., Visser, C., Snyman, M.A., Soma, P. & Muchadeyi, F.C., 2019. Genomic evaluation of resistance to
Haemonchus contortus in a South African Dohne Merino flock. Small Ruminant Research 175, 117-125.
Snyman, M.A. & Fisher, A.D., 2019. Genetic parameters for traits associated with resistance to Haemonchus contortus
in a South African Dohne Merino sheep flock. Small Ruminant Research 176, 76-88.
Snyman, M.A. & Fisher, A.D., 2019. Genetic parameters for faecal egg count, Famacha© score and body condition
score in a Dohne Merino sheep flock subjected to high levels of Haemonchus contortus. Grootfontein Agric 19(1),
31-45.
Snyman, M.A., Dlamini, N.M., Visser, C., Muchadeyi, F.C. & Soma, P., 2019. Genetic variation in resistance to
Haemonchus contortus in the Wauldby and Grootfontein Dohne Merino flocks. Grootfontein Agric 19(1), 20-30.
Snyman, M.A. & Fisher, A.D., 2019. Protocol for selection for resistance to Haemonchus contortus in South African
Dohne Merino sheep. https://rmrdsaonline.co.za/genetic-markers-for-haemonchus-contortus-in-sheep/
Snyman, M.A. & Fisher, A.D., 2020. Practical breeding for resistance and resilience to Haemonchus contortus in
South African sheep. Grootfontein Agric 20(1), 28-35.
CONCLUDING REMARKS
The project is running according to the project protocol. The developed protocols need to be validated on various farms
before they can be implemented on a wider scale.
ACKNOWLEDGEMENTS
The following people / institutions are acknowledged for their contribution to this project:
• Mr Robbie Blaine for all his inputs
• Dr Alan Fisher for all his inputs
• Dr Werner Wentzel for his inputs
• RMRD-SA and ARC for funding of the project.
16
Measurement of morphometric traits and assessment of subjective traits determining body
conformation at various ages in Dohne Merino sheep
M. A. Snyman
AIM AND OBJECTIVES
The aim of this project is to evaluate different morphometric and subjective traits determining body conformation in
Dohne Merino sheep and to determine any change in these traits with an increase in age of the animal.
The objectives of this project are to:
• Measure different morphometric traits and assess different subjective traits at various ages in ram lambs of the
Grootfontein Dohne Merino stud
• Define body conformation in terms of the most suitable combination of traits
• Award a subjective conformation score as well as a Dohne Merino Breeders’ Society classification symbol to
each animal
• Estimate the repeatability and heritability of the respective individual and combination of traits
• Estimate repeatability of the subjective conformation scores among and within judges
• Determine phenotypic trends in the conformation traits with age and the subsequent influence on
conformation scores
• Determine which of the traits contribute the most to the subjective conformation scores and to body weight
• Estimate genetic correlations of the morphometric and subjective traits with the economically important
productive traits.
BACKGROUND
Visual appraisal of animals during classing and selection has been done ever since animals have been selected for
improved performance. Apart from the economically important traits such as reproduction, body weight, fleece weight
and the wool quality traits that can be objectively measured, other traits are also considered during selection. In many
instances more emphasis is placed on the latter traits during selection than on the objectively measured traits. Body
conformation, as an indication of carcass conformation, is one of the subjective traits on which a lot of emphasis is
placed during selection. For example, in the South African Merino breed, a subjective wool score and subjective
conformation score are awarded during classing. In the Dohne Merino breed, body conformation also plays an
important role when awarding the classification symbol of an animal. Many animals that actually qualify for an AA
symbol based on their productive performance are not awarded AA symbols based on conformation. This could lead to
animals with superior genetics for the economically important production traits being culled on the basis of
subjectively assessed traits and assessor preference.
MATERIALS AND METHODS
Different morphometric body conformation traits (Table 1) were measured and assessed at 4, 8 and 12 months of age
in the 2018-born ram lambs of the Grootfontein Dohne Merino stud. A subjective conformation score was also
awarded to each animal. Body weight and body condition score of the animals were also recorded at each age. At 12
months of age, a classification symbol was also awarded by each judge, while a final classification symbol was
awarded by Judge A at 14 months of age during final classing of the animals.
Table 1. Traits measured and assessed plus the abbreviations for the traits used in the text
Trait Trait abbreviation at 4
months
Trait abbreviation at
8 months
Trait abbreviation at
12 months
Wither height (cm) Wheight4 Wheight8 Wheight12
Rump height (cm) Rheight4 Rheight8 Rheight12
Body length (cm) Blen4 Blen8 Blen12
Rump length (cm) Rlen4 Rlen8 Rlen12
Body depth (cm) Bdepth4 Bdepth8 Bdepth12
Front cannon bone length (cm) Cblen4 Cblen8 Cblen12
Shoulder width (cm) Swidth4 Swidth8 Swidth12
Rump width (cm) Rwidth4 Rwidth8 Rwidth12
Hindquarter width (cm) Hwidth4 Hwidth8 Hwidth12
Head length (cm) Headlen4 Headlen8 Headlen12
Heart girth (cm) Hgirth4 Hgirth8 Hgirth12
Abdominal circumference (cm) Abdom4 Abdom8 Abdom12
Body condition score BCS4 BCS8 BCS12
Conformation of the head Head4 Head8 Head12
17
Trait Trait abbreviation at 4
months
Trait abbreviation at
8 months
Trait abbreviation at
12 months
Pigmentation Pigm4 Pigm8 Pigm12
Hocks Hocks4 Hocks8 Hocks12
Front pasterns Fpast4 Fpast8 Fpast12
Hind pasterns Hpast4 Hpast8 Hpast12
Top line Topl4 Topl8 Topl12
Body conformation - Judge A CS-A4 CS-A8 CS-A12
Body conformation - Judge B CS-B4 CS-B8 CS-B12
Body conformation - Judge C CS-C4 CS-C8 CS-C12
Classification symbol - Judge A SYM-A
Classification symbol - Judge B SYM-B
Classification symbol - Judge C SYM-C
Final classification symbol SYM
Birth weight (kg) BW
42-day weight (kg) W42
100-day weaning weight (kg) WW
4-month weight (kg) W4
8-month weight (kg) W8
12-month weight (kg) W12
RESULTS
Phenotypic correlations estimated among conformation traits recorded at 4, 8 and 12 months of age are presented in
Table 2. The highest correlation was obtained for body weight. Correlations lower than 0.50 were estimated between 4
and 8 months and between 4 and 12 months for body conformation score by two of the judges. Correlations above 0.50
among all three combinations were only obtained for Wheight, Rheight, Blen, Hgirth, Pigm, CS-A and body weight.
Table 2. Correlations between conformation traits recorded at 4, 6 and 12 months of age
Trait Correlation between 4 and
8 months
Correlation between 4 and
12 months
Correlation between 8 and
12 months
Wheight 0.73* 0.61* 0.65*
Rheight 0.73* 0.60* 0.66*
Blen 0.51* 0.56* 0.63*
Rlen 0.34* 0.24* 0.26*
Bdepth 0.56* 0.50* 0.48*
Cblen 0.18* -0.01 0.32*
Swidth 0.33* 0.30* 0.39*
Rwidth 0.12 0.16 0.11
Hwidth 0.38* 0.25* 0.35*
Headlen 0.41* 0.39* 0.44*
Hgirth 0.62* 0.52* 0.64*
Abdom 0.53* 0.45* 0.51*
BCS 0.32* 0.10 0.24*
Head 0.47* 0.23* 0.38*
Pigm 0.66* 0.63* 0.80*
Hocks 0.17* 0.06 0.09
Fpast 0.09 0.03 0.05
Hpast -0.04 -0.09 0.08
Topl 0.19 0.16 0.23
CS-A 0.57* 0.55* 0.59*
CS-B 0.45* 0.48* 0.51*
CS-C 0.50* 0.42* 0.60*
Body weight 0.81* 0.70* 0.90*
* Significant correlation
The results of the forward stepwise regression of conformation traits, some wool traits and body weight recorded at 12
months of age on the final classification symbol are presented in Table 3. Conformation score (CS-A12), Head12 and
18
Wool score explained most of the variance in the final classification symbol, with conformation and wool score
contributing 65% of the variance.
Table 3. Stepwise regression of conformation traits (including conformation score), some wool traits and body weight
recorded at 12 months of age on the final classification symbol
Trait Regression
coefficient Partial R2 Model R2 P value
Intercept 1.81
CS-A12 0.53 ± 0.04 0.4670 0.4670 0.0001
Wool score 0.25 ± 0.02 0.1811 0.6481 0.0001
Head12 0.05 ± 0.01 0.0605 0.7086 0.0001
Hwidth12 -0.07 ± 0.03 0.0211 0.7297 0.0001
Wheight12 -0.06 ± 0.02 0.0119 0.7416 0.0010
Pigm12 -0.01 ± 0.01 0.0087 0.7503 0.0039
Blen12 0.06 ± 0.02 0.0085 0.7588 0.0061
Swidth12 -0.11 ± 0.04 0.0084 0.7672 0.0071
Testis 0.02 ± 0.01 0.0038 0.7710 0.0550
The percentage of rams that were awarded each 12-month and final classification symbol vs the percentage of rams
that qualified for each classification symbol according to their selection index is presented in Table 4. It is evident that
the majority of rams are culled on the basis of subjective assessment.
Table 4. The percentage of rams that were awarded each 12-month and final classification symbol vs the percentage of
rams that qualified for each classification symbol according to their selection index
Symbol Classification symbol according
to the selection index
Classification symbol at 12
months of age Final classification symbol
AA 53.4 16.5 6.8
A 39.8 40.1 28.8
B 6.8 24.0 5.1
C 19.4 59.3
In Figure 1 the body conformation scores awarded by Judge A at 4, 8 and 12 months of age are compared to the
classification symbol awarded to that animal at 12 months of age. The animals that were awarded AA or A symbols
generally got higher body conformation scores from 4 months of age. There was also less variation among the AA and
A animals in the earlier body conformation scores than among the B and C animals.
DISCUSSION
The average conformation scores of Judges A and B were higher at 8 months of age than at 4 months of age, and
remained the same at 12 months of age. The average conformation score of Judge C was also higher at 8 months of age
than at 4 months of age, but the 12-month score was lower and the same as the 4-month score. Phenotypic correlations
between 0.42 and 0.60 were obtained for the body conformation scores of the judges between the different ages.
Medium repeatability estimates between 0.40 and 0.50 for body conformation score were obtained for the three judges
over the study period.
Phenotypic correlations estimated between conformation traits and body weights were significant for most of the
measured morphometric traits and body conformation scores, but not significant for the subjectively evaluated traits.
Positive correlations higher than 0.50 were estimated between body weight and the conformation scores and
classification symbols allocated by the various judges, indicating higher scores allocated to bigger animals.
Phenotypic correlations obtained among the recorded traits at all ages were significant for most of the measured
morphometric traits, body conformation and the classification symbol awarded at 12 months of age, but not significant
for the subjectively evaluated traits Pigm, Hocks, Fpast, Hpast and Topl. Positive correlations higher than 0.50 were
obtained between Hgirth and Abdom and many of the other traits related to skeletal dimensions. The subjective Head
score was also positively related to many of these traits.
19
0
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AA Classification at 12 months A Classification at 12 months
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B Classification at 12 months C Classification at 12 months
Figure 1. Body conformation scores awarded by Judge A at 4, 8 and 12 months of age of the animals awarded the
different classification symbols at 12 months of age
At 8 and 12 months of age, only Blen, Hgirth and Head had positive correlations higher than 0.50 with the body
conformation scores of the judges. Generally, positive correlations above 0.50 were estimated among the conformation
scores and classification symbols allocated by the various judges. The Dohne Merino classification symbol only had a
positive correlation of higher than 0.50 with Blen12 and Head12, and was not correlated to many of the measured
morphometric traits.
Various stepwise regression analyses were done with body weight, body conformation score of each judge at each age,
classification symbol awarded by each judge at 12 months of age and final classification symbol as independent
variables. The results of the stepwise regression analyses indicated that Hgirth and Blen explained the most variance in
body weight at all three ages, while Bdepth8 also explained more than 5% of the variance in body weight at 8 months
of age.
It is evident that there was much variation among the judges in the traits contributing the most to the body
conformation score. At 4 months of age, the only trait of importance common to all three judges was Hgirth4, while at
8 months of age Head8, Swidth8, BCS8 and Blen8 were the common traits explaining variation in 8-month body
conformation scores. At 12 months of age, Head12, Blen12 and Topl12 explained the most variance in body
conformation score of all three judges. It is clear that, except for Head at 8 and 12 months of age, there was no
consistency in the traits that were taken into account when awarding the scores.
There was also variation among judges in the traits contributing to the classification symbol awarded by the judges at
12 months of age. Among the traits taken into account when awarding the symbols, were Head12, Blen12, Hgirth12
and Fpast12.
The results of the stepwise regression of morphometric traits, some wool traits and body weight recorded at 12 months
of age on the final classification symbol indicated that body conformation score (CS-A12), Head12 and Wool score
explained the most variance in the final classification symbol, with body conformation and wool score contributing
65% of the variance. These results indicate that the most emphasis is placed on subjective impressions, as there was
also no consistency in the traits contributing to the body conformation scores.
20
The repeatability within and between judges was also low. Variable scores were awarded by the different judges for
the same animal at the same age. For example, animals that got a 6 score from one judge, might get a score of between
2 and 9 from the other judges. Variable scores were also awarded by the same judge for the same animal at 4 and 8
months of age. For example, animals that got a 6 score at 4 months of age, might get a score of between 3 and 8 at 8
months of age from the same judge. This could be explained by the emphasis placed on different traits at different ages
by the different judges.
Considering the various results, it seems as if the traits receiving the most emphasis are Head, Blen and Hgirth. Blen
and Head were also two of the very few traits of which the means differed among animals that were awarded the
different final classification symbols at 12 months of age. Blen and Hgirth also contributed the most to body weight,
thus indirectly placing much emphasis on body weight. When evaluating the classification symbol as indicated by the
selection index, body weight was the only trait contributing more than 5% to the variance.
Judging from the morphometric and performance data, there is no valid reason why so few animals should be awarded
an “AA” symbol and be eligible for use in a stud. No scope is left for selection on performance data, as the majority of
the rams are culled on the basis of personal preference of the judges.
PUBLICATIONS
None to date.
CONCLUDING REMARKS
Due to the heavy work load of the technician during January 2020, the 2019 lambs were not assessed at 4 months of
age. The 8-month measurements could also not be taken due to the COVID-19 lockdown during May 2020. Therefore,
the project will not be done on the 2019-born lambs and will continue with the 2020-born lambs in January 2021 if
circumstances allowed.
ACKNOWLEDGEMENTS
The following people are acknowledged for their contribution to this project:
• The judges for assessment of body conformation
• The GADI and Small Stock Research Trust employees for collection of the conformation trait data.
21
Prediction of tail weight from tail measurements in Namaqua Afrikaner sheep
M.A. Snyman
AIM AND OBJECTIVES
The aim of this project is to predict tail weight from tail measurements in Namaqua Afrikaner sheep at various ages,
and to determine the amount of fat resources mobilised from the tail during lactation by Namaqua Afrikaner ewes.
The objectives of this project are to:
• Record length and circumference measurements of the tails of Namaqua Afrikaner sheep at various ages at the
Carnarvon Experimental Station
• Weigh tails of the above-mentioned animals after slaughtering
• Compile prediction equations for tail weight from length and circumference measurements
• Record length and circumference measurements of the tails of Namaqua Afrikaner ewes before lambing and
after weaning of their lambs
• Determine the amount of fat resources mobilised from the tail during lactation utilising the above prediction
equations.
BACKGROUND
The Namaqua Afrikaner breed is one of the few indigenous breeds for which some scientific production and
reproduction norms are available. However, little information is known on the relative weight of the fat-tails and the
metabolism of this fat during lactation or under periods of adverse feeding conditions. Information on these aspects
would contribute to the knowledge database for the indigenous breeds. The lactation cycle, especially early lactation, is
the period of highest nutrient requirements in the entire productive cycle of the ewe. As the growth of the lamb during
this period is mainly determined by its milk intake, shortage of good quality feed at this stage for the ewe could impact
negatively on lamb growth rate. The latter in turn will negatively influence profitability from meat production of the
enterprise. If fat-tailed ewes could ”supplement” their energy resources by mobilising the fat resources in their fat-tails,
this negative impact on lamb growth could be reduced.
Since 2013, below average rainfall has been recorded at the Carnarvon Experimental Station. For 2018, 206 mm rain
was recorded. Although this is average for the region, 178 mm of the rain fell from January until May 2018. For the
ensuing period until December 2019, only 72 mm rain was recorded. The lowest rainfall since 2003 was recorded
during 2019 (44 mm), with only 11 mm of rain recorded from May until December 2019. This resulted in very poor
veld conditions which necessitated the commencement of the provision of supplementary feeding to the Namaqua
Afrikaner ewes during lambing in September 2019. The ewes received chocolate maize (300 g/ewe/day) and lucerne
pellets (300 g/ewe/day) from September until the end of December 2019. It was therefore an ideal time to evaluate the
ability of the ewes to mobilise the fat reserves in their fat-tails during lactation.
However, for this to be possible in the live animals, prediction equations need to be compiled first. Due to the dry
conditions, the 2018-born lambs were classed at an earlier age (9 months of age) than usual (14 months of age). These
surplus lambs, as well as all other available older animals, were measured and slaughtered to obtain data for the
compilation of prediction equations of fat-tail weight from tail measurements in the live animal.
MATERIAL AND METHODS
Slaughter trial
Surplus 2018-born lambs, as well as all other available older animals, were measured and slaughtered to obtain data for
the compilation of prediction equations of fat-tail weight from tail measurements in the live animal. The following was
recorded on / awarded to all these animals:
• Body weight
• Upper tail circumference (UTC) - measurement taken in cm at the base of the tail.
• Lower tail circumference (LTC) - measurement taken in cm at the lowest part of the tail, just proximal to the
twist.
• Distance in cm between UTC and LTC.
• Tail length entire (TLE) - measurement taken in cm from the base of the tail to the tip of the tail on the middle
inner side of the tail. The entire tail length along the twist is measured.
• Tail length thick (TLT) - measurement taken in cm from the base of the tail to the end of the thick part of the
tail to the point where the twist starts. Measured on the middle inner side of the tail.
• Tail twist: To Left, Straight, To Right
• Extent of twist: Award Tail twist category according to Figure 1.
22
The animals were slaughtered at the local abattoir in Carnarvon, where the weight of the tail (TMAS) was recorded in
grams for each animal.
Category 1
Full corkscrew twist to the left or right
Category 2
Long tail with only an indication of twist to the left of right
Category 3
“Ronderib”-tail. Shorter tail with only the tip curling
around to the left or right. Tail ending well above the
hocks
Category 4
Straight tail having no twist
Figure 1. Description of extent of twist of the tail
For the calculation of the volume of the tail, it was divided into two parts; the cylindrical part and the tip part (cone
shaped). The volume was calculated as follows:
VOL1 (cylindrical part) = πr2h
= π x (radius of UTC)2 x DIST
VOL2 (cone shaped tip part) = πr2h/3
= π x (radius of LTC)2 x ((TLE-TLT)/3)
VOL3 (total tail volume) = VOL1 + VOL2
Least square means for all the tail measurements were obtained by fitting GLM models with fixed effects for sex, age
and tail category (TCAT). Phenotypic correlations among the tail measurements were estimated with PROC CORR of
SAS for all the data. Various regression models predicting tail weight, including the different tail volumes and the
individual tail measurements, were fitted with PROC GLM of SAS.
Lactating ewe trial
This part of the trial was done on the breeding ewe flock. The same tail trait information as for the animals in the
slaughter trial were recorded on / awarded to all ewes before lambing at the end of August 2019 and again after
weaning of the lambs in January 2020. Number of lambs born and weaned, and weight of lamb weaned per ewe were
recorded. Body weight of the ewes was recorded after weaning.
23
RESULTS AND DUSCUSSION
Slaughter trial
Phenotypic correlations among the tail measurements estimated on the entire dataset are given in Table 1. High
correlations were estimated between tail volume and TMAS, and medium to high correlations between TMAS and the
other tail measurements. For these measurements to be used as accurate predictors for tail weight, higher correlations
than those estimated in this study would have been preferred.
Table 1. Correlations among tail measurements estimated on the entire dataset (n=103)
Trait VOL1 VOL2 VOL3 UTC LTC DIST TLE TLT
TMAS 0.67* 0.58* 0.69* 0.59* 0.60* 0.48* 0.47* 0.49*
VOL1 - 0.71* 0.99* 0.90* 0.81* 0.69* 0.48* 0.39*
VOL2 - 0.81* 0.55* 0.84* 0.39* 0.72* 0.52*
VOL3 - 0.87* 0.96* 0.66* 0.57* 0.44*
UTC - 0.67* 0.47* 0.33* 0.38*
LTC - 0.41* 0.37* 0.47*
DIST - 0.58* 0.24*
TLE - 0.49*
* Significant correlations
Various linear regression models predicting tail weight are summarised in Table 2. The results in Table 2 are in
agreement with the correlations obtained above. The best predictions were obtained for the models including VOL3 or
the individual measurements, but the R2 of these models ranged from 0.46 to 0.48. A higher R2 is preferred to make
more accurate predictions. Unfortunately, the ewes declared surplus after weaning of their lambs in January 2020,
could not be slaughtered due to the COVID-19 lockdown. Some of these ewes lost weight in their tails, which would
have increased the variation in tail weight of the available data set and could probably increase the predictability of the
models.
Table 2. Linear regression models predicting tail weight
Trait Regression coefficient P value trait R2 model
Model (All data) TMAS = VOL1
Intercept 3.7783 0.4521
VOL1 0.0005 0.0001
Model (All data) TMAS = VOL2
Intercept 3.9555 0.3327
VOL2 0.0015 0.0001
Model (All data) TMAS = VOL3
Intercept 3.7648 0.4718
VOL3 0.0004 0.0001
Model (All data) TMAS = UTC + LTC + DIST
Intercept 2.6807 0.4618
UTC 0.0176 0.0091
LTC 0.0260 0.0017
DIST 0.0290 0.0116
Model (All data) TMAS = UTC + LTC + TLE
Intercept 2.6560 0.4830
UTC 0.0199 0.0019
LTC 0.0233 0.0043
TLE 0.0154 0.0013
Model (All data) TMAS = UTC + LTC + TLT
Intercept 2.8321 0.4704
UTC 0.0205 0.0016
LTC 0.0215 0.0107
TLT 0.0209 0.0048
Lactating ewes
Least square means for the tail measurements of the ewes before and after lactation are presented in Table 3.
Significant differences in tail volume and some measurements were observed before and after lactation in the ewes,
indicating weight loss in the fat-tails. The ewes had an average body weight loss of 4.6 kg between mating and post
weaning.
24
Table 3. Least square means for the tail measurements of the ewes before and after lactation
Trait Before lactation After lactation
UTC (cm) 31.1a ± 0.5 24.5a ± 0.5
LTC (cm) 22.4a ± 0.4 19.7a ± 0.4
DIST (cm) 20.1a ± 0.3 18.4a ± 0.3
TLE (cm) 32.0 ± 0.5 32.7 ± 0.5
TLT (cm) 20.1 ± 0.4 19.5 ± 0.4
VOL1 (cm3) 1597a ± 50 881a ± 50
VOL2 (cm3) 164a ± 9 136a ± 9
VOL3 (cm3) 1761a ± 55 1017a ± 55 a Values with the same superscripts within traits differ significantly (P <0.05)
The effects of number of lambs born and number of lambs weaned on the reduction in tail volume during lactation are
presented in Table 4. Linear regression of total weight of lamb weaned on reduction in tail volume during lactation is
given in Table 5. From Tables 4 and 5 it is evident that the number of lambs born or weaned, or the kilogram of lamb
weaned, did not influence the volume of fat mobilised from the fat-tail during lactation. Supplementation of the ewes
during lactation could have influenced these results.
Table 4. Effects of number of lambs born and number of lambs weaned on the reduction in tail volume during lactation
Trait Reduction in VOL1 Reduction in VOL2 Reduction in VOL3
Number of lambs born
0 -756 ± 139 -26 ± 27 -783 ± 153
1 -657 ± 83 -27 ± 16 -684 ± 91
2 -772 ± 94 -30 ± 18 -803 ± 103
3 -767 ± 575 5 ± 112 -762 ± 629
Number of lambs weaned
0 -724 ± 117 -32 ± 23 -755 ± 127
1 -673 ± 82 -19 ± 16 -692 ± 89
2 -782 ± 104 -39 ± 20 -820 ± 114
Table 5. Linear regression of total weight of lamb weaned (TWW) on reduction in tail volume during lactation
Trait Regression coefficient P value trait R2 model
Model Reduction in VOL1 = TWW
Intercept -728 0.0002
Reduction in VOL1 0.5342 0.8994
Model Reduction in VOL2 = TWW
Intercept -29 0.0000
Reduction in VOL2 0.0472 0.9540
Model Reduction in VOL3 = TWW
Intercept -756 0.0002
Reduction in VOL3 0.5790 0.9002
PUBLICATIONS
None to date.
CONCLUDING REMARKS
This project is running according to the project protocol. The slaughtering of more animals with varying tail weights
will contribute to variation in the dataset and more accurate prediction equations.
ACKNOWLEDGEMENTS
The following people are acknowledged for their contribution to this project:
• Personnel of the Northern Cape Department of Agriculture, Land Reform and Rural Development at the
Carnarvon Experimental Station for maintenance of the animals and collection of data
• Personnel from GADI for collection of data.
25
Description and comparison of different mating and kidding systems used in the South
African Angora goat industry
J.H. Hoon and A. Baca
AIM AND OBJECTIVES
The aim of this project is to describe and compare the different Angora mating and kidding systems used in the South
African Angora goat industry.
The objectives of this project are to:
• Describe the practices related to different mating systems, where these practices will also include labour,
financial, health, management and feeding aspects
• Describe the practices related to different kidding systems, where these practices will also include labour,
financial, health, management, feeding and predator control aspects
• Compare the different practices with regard to labour requirements and cost effectiveness
• Identify advantages and disadvantages of each system
• Identify possible areas that need further research
• Incorporate these descriptions and findings into the Mohair Production modules for the Grootfontein Diploma
course
• Use the results of this investigation to provide sound advice to Angora goat producers across the farming
spectrum.
BACKGROUND
Various mating and kidding systems are followed in the South African Angora goat industry, each with its advantages
and disadvantages. Mating systems vary from flock mating with no pedigree recording to individual sire mating and
artificial insemination (AI). Kidding can take place in the veld, on pastures, in kraals or in individual kidding pens.
Due to predators that are becoming a bigger problem, more and more producers are implementing some version of the
individual pen kidding system. Although many producers make use of an individual pen kidding system, producers still
have many questions about the viability and especially the cost aspects of this system in comparison with the other
systems. In practice, it often happens that many producers may make use of the same basic system, but they follow
different management practices and have different infrastructures available for each system. This project is being done
to describe and compare the different Angora goat mating and kidding systems used in the South African Angora goat
industry. Angora goat producers that apply different mating and kidding systems were identified for participation in
this project. The identification process was done in collaboration with the South African Mohair Growers’ Association.
Six Angora goat producers were identified as participants in 2017 and a further six in 2018. The study is conducted on
the ewe flocks and their progeny of the participating Angora goat producers.
MATERIALS AND METHODS
The 12 participants were visited twice, once during the mating season and once during the kidding season. During the
two visits, interviews were conducted with the producers and the Mating systems and Kidding systems questionnaires
were completed. Photos of the veld, animals and infrastructure relating to mating and kidding, were also taken. The 12
participants visited during the 2017 and 2018 mating seasons are given in Table 1.
Table 1. Participating Angora farmers
Participant No Dates visited
Mating Kidding
Mr Hans Greeff (GADI) 1 09 March & 08 May 2017 28 August 2017
Mr Richard Herold (Graaff-Reinet) 2 15 March 2017 29 August 2017
Mr Roelfie van der Merwe (Aberdeen) 3 16 March 2017 21 August 2017
Mr Paul Broeksma (Aberdeen) 4 30 March 2017 06 September 2017
Mr Fransie Fourie (Jansenville) 5 27 April 2017 13 September 2017
Mr Ross Henderson (Steytlerville) 6 04 May 2017 12 September 2017
Mr Jordi van Hasselt (Prins Albert) 7 23 March 2018 21 September 2018
Mr Gary Hobson (Steytlerville) 8 20 April 2018 18 September 2018
Mr Jan Nel (Aberdeen) 9 24 April 2018 19 September 2018
Mr Jan Lategan (Aberdeen) 10 26 April 2018 25 September 2018
Mr Boeta Grobler (Murraysburg) 11 14 May 2018 10 October 2018
Mr Fred Colborne (Willowmore) 12 15 May 2018 18 September 2018
26
DESCRIPTION OF KIDDING SYSTEMS
Mr Hans Greeff, Grootfontein Student Angora Stud, Middelburg, EC
A combination of small camps/kraals and individual pens is used. After shearing (2 to 3 weeks before kidding), the
young ewes and ewes pregnant with twins are kept at a shed with kraals and individual pens on the GADI premises,
while the ewes pregnant with single kids are moved to a camp with a shed in the veld. The single ewes are moved into
the pens in the shed once they have kidded, while the twin ewes kid in the kraals at the shed (30 to 40 ewes per kraal).
Once the twin ewes have kidded, they are moved to individual pens in the kraals and from there to individual pens
inside the shed. The ewes with single kids are kept in the individual pens for 3 to 4 days. The ewes with twins are kept
in the pens for 5 to 6 days and ewes with triplets for 10 to 14 days, after which they are moved back to the kraals in
groups of ~ 20 for approximately 1 week. These groups of ~ 20 ewes with their kids are moved to small veld camps (~
2 ha) for another 3 weeks before they are put into the larger camps.
Mr Richard Herold, Graaff-Reinet
A combination of small camps/kraals and cultivated pastures is used. The ewes are moved from the veld to the small
camps and pastures approximately one week before kidding. The single and twin ewes kid separately in small camps.
The singles ewes and their kids are moved to the pastures after 2 to 3 days, while the twin ewes and their kids stay in
the small camps for 2 weeks before they are moved to the pastures. The average size of the pasture camps is 3 ha. The
single ewes and their kids are moved from the pastures to the veld after 3 to 4 weeks, while the twin ewes remain on
the pastures until weaning.
Mr Roelf van der Merwe, Aberdeen
A combination of small camps/kraals, individual pens and cultivated pastures is used. The stud ewes are kept on
cultivated pastures for the whole year, while the flock ewes are moved from the veld to the small camps and pastures
approximately one week before kidding. The twin ewes kid in small camps and the ewes and their kids are moved into
individual pens in the camps for 2 to 3 days, after which they are moved to the pastures. The average size of the
pasture camps is 1 to 5 ha. The single and twin flock ewes and their kids are kept on the pastures until weaning, while
the stud ewes remain on the pastures.
Mr Paul Broeksma, Aberdeen
A combination of veld, small camps and individual pens is used. The single ewes kid in the veld in groups of ~ 100
animals in camps of ~ 120 ha. The twin ewes are moved into small veld camps after shearing, 3 to 4 weeks before
kidding. Once they have kidded, they are moved to individual pens where they are kept for 5 to 10 days. In the
individual pens, the ewes and their kids are allowed to move out of the individual pens during the day to a larger area.
After this period, the ewes are grouped together again and moved to small veld camps.
Mr Fransie Fourie, Jansenville
A system of small camps in veld, close to the homestead, is used. All the ewes (singles and twins) kid in the veld in
small camps. The pregnant ewes are put into small veld camps (~ 10 ha) 3 to 4 weeks before kidding. Groups of 35 to
50 animals are put into one camp, depending on the size of the camp. The ewes and their kids stay in the small camps
for 3 to 4 weeks after kidding. The smaller groups of animals are then grouped together and moved to larger veld
camps.
Mr Ross Henderson, Steytlerville
A combination of veld, small camps/kraals and individual pens is used. The single ewes kid in the veld in groups of 75
to 80 animals in camps of ~ 100 ha. The twin ewes and young ewes kid in small veld camps (50 x 50 m) in groups of
10 to 15 animals. After kidding, the twin ewes are put into individual pens inside the small camp for 2 to 3 days, while
the young ewes are not put into the individual pens. These small camps have low outside fences, allowing the ewes to
go out to graze during the day while the kids stay behind. The ewes and kids are kept in these small camps for one
week before they are moved back to the larger camps in the veld.
Mr Jordi van Hasselt, Prince Albert
A combination of veld and pastures is used. The single flock ewes kid on the veld in large camps of 500 to 1000 ha.
Once they have kidded, the ewes and their kids are moved to smaller veld camps where they are kept in groups of 30 to
60 ewes, depending on the size of the camps. The stud ewes and twin flock ewes kid on cultivated pastures in camps of
0.5 to 1.0 ha. The ewes are moved to the kidding camps on the pastures about one week before kidding. After kidding,
the single stud ewes are kept in groups of 40 animals, while the twin ewes (flock and stud) are kept in groups of 20
animals. They are kept on the pastures for a period ranging from 1 to 4 weeks after kidding, depending on the pasture
availability and the condition of the veld, after which they are moved to the veld camps.
27
Mr Gary Hobson, Steytlerville
A combination of kraals (where ewes go out during the day and kids stay in the kraal) and individual pens is used. All
the ewes kid in small camps in the veld. Within 6 hours after kidding, the ewes and their kids are moved to the kraals.
Initially five ewes with newborn kids are placed in a kraal and an additional five ewes are added each day. A maximum
of 40 to 50 ewes are kept per kraal. The single ewes stay in the kraals while the young ewes and twin ewes are put into
individual pens for 1 to 2 days. After this period, the young ewes and twin ewes are put back into the kraals. For the
first 3 to 4 days after kidding, the ewes and kids are kept together in the kraal, after which the ewes go out to the veld
during the day while the kids stay behind in the kraals. After ~ 2 weeks after kidding, the kids go out to the veld
together with the ewes. Once the kids are strong enough, the ewes and kids are moved to larger veld camps.
Mr Jan Nel, Aberdeen
A combination of small camps/kraals and individual pens is used. All the ewes kid in veld or pasture camps (2 to 4 ha)
in groups of up to 100 animals. The ewes are put into the camps ~ 1 week before kidding. After kidding, the single
ewes and their kids are moved to other small camps with pastures while the twin ewes and their kids are moved to the
kidding shed with individual pens. The twin ewes are kept in the individual pens for ~ 7 days after which they are
moved out of the shed into a small camp/kraal where they are supplied with the same feed as in the individual pens.
After a few days, the ewes and their kids are moved back to the camps with pastures. The single and twin ewes stay on
the pastures for as long as possible, depending on pasture availability, before they are moved to larger veld camps.
Mr Jan Lategan, Aberdeen
A combination of pastures and individual pens is used. All the ewes kid on cultivated pastures in groups of 300 to 400
animals in camps of 4 to 5 ha. The ewes are put into the camps 1 week before kidding. After kidding the twin ewes and
their kids are moved to individual pens. The twin ewes are kept in the individual pens for 4 to 5 days after which they
are moved to small camps/kraals for 7 to 14 days, where they receive a total mixed ration. The twin ewes and kids are
moved back to the camps with cultivated pastures. All the ewes and their kids stay on the pastures for 6 to 8 weeks
before they are moved to veld camps.
Mr Boeta Grobler, Murraysburg
A combination of veld and pastures is used. The single flock ewes kid in the veld in groups of 50 to 125 animals,
depending on the camp size, in camps ranging from 10 to 50 ha. The ewes are moved to the kidding camps after
shearing, two to four weeks before kidding. The select flock ewes and twin ewes kid on cultivated pastures in camps of
1 to 3 ha. The ewes are moved to the kidding camps two weeks before kidding. The single select flock ewes are kept in
groups of 125 animals while the twin ewes are kept in groups of 50 to 60 animals. The ewes and their kids are kept on
the pastures until 3 to 4 weeks after kidding, depending on pasture availability and the condition of the veld, after
which they are moved to veld camps.
Mr Fred Colborne, Willowmore
A combination of pastures and small camps is used. The ewes kid on cultivated pastures in camps of ~ 7 ha. The single
ewes are kept in groups of 40 to 60 animals while the twin ewes are kept in groups of 10 to 15 animals in smaller
camps. The ewes are moved to the kidding camps two weeks before kidding, just after shearing. The ewes and their
kids are kept on the pastures for 6 to 8 weeks after kidding, depending on pasture availability and the condition of the
veld, after which they are moved to veld camps.
DESCRIPTION OF WEANING SYSTEMS
The management practices during lactation and weaning are summarised in Table 2.
PUBLICATIONS
None to date.
CONCLUDING REMARKS
The Weaning systems questionnaires have been completed in the reporting year and the reproduction data of most of
the participating Angora goat flocks have been obtained. However, information obtained from the questionnaires with
regard to aspects such as health (vaccinations, internal and external parasites), nutrition (supplementary feeding, creep
feeding, flush feeding, lambing pen feeding), management (shearing, culling, predator control), infrastructure, labour,
advantages and disadvantages of the different systems, still need to be processed.
ACKNOWLEDGEMENTS
The participating producers are acknowledged for their contribution to the project.
28
Table 2. Management practices followed during lactation and weaning by the 12 participants
P
rod
uce
r
La
cta
tio
n
Cre
ep f
eed
ing
Wea
nin
g
pra
ctic
e
1 Single and twin ewes receive the same
supplementation. Creep feeding to all kids from 4 to 6 weeks of age.
Ewes are taken out and kids stay in the camps that they are
familiar with.
2
Twin ewes receive more supplementary feed and
are kept longer on the planted pastures before they
are moved to the veld.
Creep feeding to all kids from 2 weeks of age. Kids are moved back to the planted pastures, with
supplementary feeding.
3
Single and twin ewes receive feed pellets and
lucerne hay on planted pastures, but the twin ewes
receive larger amounts.
Creep feeding to all kids from 4 weeks before
weaning.
Ewes are taken out and kids stay in the camps that they are
familiar with. A few mature ewes (5-10), normally ewes with
smaller kids, are kept with each kid group.
4
With poor veld conditions, single and twin ewes
receive supplementary feeding, but only twin ewes
receive supplementary feeding with good veld
conditions.
Creep feeding from 2 to 4 weeks of age only for
twin kids and kids of 2-tooth ewes.
Kids are divided into three groups at weaning: twins, singles
and mixed (all the smaller/weaker kids). Three mature, dry ewes
are put with each kid group.
5
Single and twin ewes receive feed pellets in small
lambing camps but the twin ewes receive larger
amounts.
Creep feeding to all kids from 2 to 3 weeks of age. Ewes are taken out and kids stay in the camps that they are
familiar with.
6 Twin ewes receive a feed mixture with higher
bypass protein content than the single ewes.
Creep feeding to twin kids from 3 weeks of age;
single kids only receive creep feeding when veld
conditions are poor.
Ewes are taken out and kids stay in the camps that they are
familiar with. A couple of old/dry ewes are kept with each kid
group.
7
Singles ewes kid on veld while twin ewes kid on
planted pastures. Both groups receive
supplementary feeding; the type and amount will
depend on the grazing conditions.
Creep feeding to all kids from 2 weeks of age.
Ewes are taken out and kids stay in the camps that they are
familiar with. A few mature ewes are kept with each kid group
in the veld camps for ~ 3 weeks.
8
Single and twin ewes receive chocolate maize and
production lick but twin ewes receive larger
amounts.
Creep feeding to all kids from 4 weeks of age. Ewes are taken out and kids stay in the camps that they are
familiar with.
9 Twin ewes receive a feed mixture with higher
bypass protein content than the single ewes. Creep feeding to all kids from 2 months of age.
Ewes are taken out and kids stay in the camps that they are
familiar with.
10 All ewes are kept on planted pastures and do not
receive supplementary feeding during this period. Kids do not receive creep feeding during lactation.
At weaning, kids of one group are swopped with kids from
another group. The ewes are kept for ~ 2 weeks with the kids in
this way.
29
Pro
du
cer
La
cta
tio
n
Cre
ep f
eed
ing
Wea
nin
g
pra
ctic
e
11
Singles ewes kid on veld while twin ewes kid on
planted pastures. Both groups receive
supplementary feeding; the type (chocolate maize
and/or production lick) and amount will depend on
the grazing conditions.
Kids do not receive creep feeding during lactation. At weaning, kids from different ewe groups are grouped
together in larger groups (up to 500) and moved to new camps.
12
On good pastures, only twin ewes receive chocolate
maize while both groups receive feed pellets in
different amounts on poor pastures.
Creep feeding to all kids from 6 weeks of age.
Ewes are taken out and kids stay in the camps that they are
familiar with. A few young goats or old ewes are put with each
kid group.
30
Studies on the detection, control by vaccination and the genetics of Ovine Johne’s Disease
W.J. Olivier
AIM AND OBJECTIVES
The aims of this project are to evaluate the methods of detecting Ovine Johne’s Disease (OJD) and the effect of
vaccination against OJD on the control of the disease, as well as to quantify the genetics of OJD.
The objectives of this project are to:
• Determine the level of infection of the animals in the Cradock fine wool Merino stud
• Determine the sensitivity of the enzyme-linked immunosorbent assays (ELISA) test compared to
histopathological evaluations
• Determine the repeatability of the ELISA test results
• Evaluate the effect of vaccination against OJD on the control of the disease
• Determine the effect of vaccination against OJD on production and reproduction traits
• Estimate the heritability of the incidence of OJD and correlations with production and reproduction traits.
BACKGROUND
Two South African ovine genetic resource flocks are currently diagnosed positive for OJD, namely the Cradock fine
wool Merino stud and the Langgewens crossbreeding Merino-type flock. Blood samples of all ewes in the respective
flocks are already available in the biobanks at Grootfontein and Elsenburg, where it is maintained at minus 80 ˚C.
Blood samples of replacement ewes entering the breeding flock will be obtained annually and included in the
respective biobanks. Complete pedigree and production information is available for all animals. The OJD positive
status of these two flocks has created the opportunity to improve the paucity of information on the detection,
vaccination and genetics of OJD in local sheep flocks through research. This report covers the Cradock fine wool
Merino part of the project.
RESULTS AND DISCUSSION
Since 2017, 50 ram and 50 ewe weaned lambs (from the 2016-born lambs) were inoculated with Gudair® vaccine. The
lambs were divided in Inoculated and Not Inoculated groups on a stratified body weight basis. Weaning weight,
corrected for age and gender, were used to divide the animals.
In 2019, 140 surplus young and culled older animals were slaughtered. The percentage of animals confirmed positive
or negative with histopathology according to age and OJD inoculation status are summarised in Table 1. A total of 43
animals were confirmed positive for OJD with histopathology from the 140 animals that were slaughtered during 2019.
It is evident from Table 1 that 30% of the young animals (born in 2017) and 38% of the adult animals (born before
2017) slaughtered during 2019 were confirmed positive for OJD.
Table 1. Percentage of animals confirmed positive or negative with histopathology according to age and OJD
inoculation status
Status Age (140) OJD Inoculated (46)
Young1 (119) Adult2 (21) Young (45) Adult (1)
OJD Negative 70.59% (84) 61.90% (13) 77.78% (35) 0.00%
OJD Positive 29.41% (35) 38.10% (8) 22.22% (10) 100.00% (1)
Total inoculated 97.83% 1.17% 1 Animals born in 2017; 2 Animals born before 2017
Forty-six of the 140 animals that were slaughtered were inoculated against OJD, of which 98% were young animals.
The low number of adult ewes (born before 2017) is due to the fact that the 2015-born animals were the first group that
was inoculated. The only inoculated adult ewe that was slaughtered tested positive for OJD, while 22% (10) of the
young animals that were inoculated tested positive.
Faecal and tissue samples were also collected during the reporting period on the 140 animals that were culled and
slaughtered. The results of the Ziehl Neelsen Stain smears of the faeces and small intestine and histopathology of the
intestine samples are summarised in Table 2. It is evident from Table 2 that approximately 31% of the animals
slaughtered were confirmed to be positive for OJD with histopathology, while between 26% and 29% of the animals
slaughtered were positive or suspicious for OJD with the other two tests.
31
Table 2. Faecal and intestine Ziehl Neelsen Stain smears and histopathology results of the 140 animals slaughtered
Status Histopathology
(%) Faecal smear (%) Intestine smear (%)
OJD Negative 69.29% (97) 70.83% (102) 73.94% (105)
OJD Suspicious - 18.06% (26) 12.68% (18)
OJD Positive 30.71% (43) 11.11% (16) 13.38% (19)
The results of the faecal and small intestine Ziehl Neelsen Stain smears of the 43 animals confirmed OJD positive with
histopathology are summarised in Table 3. The intestine smears had the highest correlation with the histopathology
results, with 44% of the OJD positive animals having positive or suspicious intestine smears.
Table 3. Faecal and intestine Ziehl Neelsen Stain smears of the 43 histopathology confirmed OJD positive animals
Status Histopathology
(%) Faecal smear (%)a Intestine smear (%)
OJD Negative - 60.98% (25) 55.81% (24)
OJD Suspicious - 26.83% (11) 13.95% (6)
OJD Positive 100.00% (43) 12.20% (5) 30.23% (13) a Two of the 43 animals had no faecal samples
The results of the faecal and small intestine Ziehl Neelsen Stain smears of the 97 animals confirmed OJD negative with
histopathology are summarised in Table 4. Approximately 24% of OJD negative animals were tested positive with the
faecal smears test, which can be done on the live animal. This is the so-called false positive results from the tests on
live animals, which is a big problem when testing for OJD. Furthermore, the large percentage of OJD confirmed
positive animals that was not detected on live animals (Table 3), suggests that these two tests on live animals are
unreliable.
Table 4. Faecal and intestine Ziehl Neelsen Stain smears of the 97 histopathology confirmed OJD negative animals
Status Histopathology
(%) Faecal smear (%) Intestine smear (%)
OJD Negative 100.00% (97) 75.79% (72) 82.47% (80)
OJD Suspicious - 12.63% (12) 11.34% (11)
OJD Positive - 11.58% (11) 6.19% (6)
The growth and wool production of the two groups are summarised in Table 5, while the body dimension
measurements are presented in Table 6. It is evident from these two tables that only body weight, body height and front
cannon bone length differed significantly between the two groups.
32
Table 5. Body weights and wool production1 (± s.e.) of the lambs born from 2016 to 2019
Trait Inoculated Not Inoculated
Number of lambs alive at weaning (2016-2019) 307 307
Number of lambs alive at 12-months of age (2016-2018) 190 184
Weaning weight (kg) 27.5 ± 0.1 27.5 ± 0.1
6-month body weight (kg) 32.1 ± 0.4 31.7 ± 0.4
8-month body weight (kg) 39.5 ± 2.6 38.5 ± 2.6
12-month body weight (kg) 58.5 ± 1.3 57.9 ± 1.4
Body weight (kg) 61.2a ± 1.2 59.8a ± 1.2
Greasy wool (kg) 5.3 ± 0.2 5.2 ± 0.2
Clean wool (kg) 3.5 ± 0.1 3.4 ± 0.2
Clean yield (%) 65.4 ± 1.0 65.9± 1.0
Staple length (mm) 85.7 ± 1.2 86.2 ± 1.3
Fibre diameter (µm) 17.0 ± 0.2 17.1 ± 0.2
Crimps / 25 mm 13.2 ± 0.4 13.2 ± 0.3
Duerden 83.7 ± 0.9 84.0 ± 0.9
Standard deviation of fibre diameter (µm) 2.5 ± 0.1 2.5 ± 0.1
Coefficient of variation of fibre diameter (%) 14.7 ± 0.3 14.9 ± 0.3
Comfort factor (%) 99.8 ± 0.0 99.8 ± 0.0
Pleat score 6.5 ± 0.3 6.5 ± 0.3
Staple strength (N/Ktex) 43.6 ± 2.2 45.2 ± 2.3 1 Alive at 13-months of age; a Values with the same superscript differed significantly (P <0.05)
Table 6. Body dimension measurements (± s.e.) of the lambs born from 2016 to 2018 (13 months of age)
Trait Inoculated Not inoculated
Body length (cm) 84.7 ± 1.0 84.0 ± 1.0
Body height (cm) 75.8a ± 1.2 74.0a ± 1.2
Front cannon bone length (cm) 15.8a ± 0.2 15.4a ± 0.3
Heart girth (cm) 99.9 ± 1.1 100.7 ± 1.1 a Values with the same superscript differed significantly (P < 0.05)
PUBLICATIONS
None to date.
CONCLUDING REMARKS
The project is running according to the project proposal and all the data were recorded. It is evident from the results
that the indicator tests on live animals are not accurate.
ACKNOWLEDGEMENTS
The author extends his gratitude to Cape Wools SA for partial funding of the project and the Department of Rural
Development and Agrarian Reform of the Eastern Cape for assistance with the execution of the project.
33
Establishment of the South African biological reserve for small stock research and
conservation
M.A. Snyman
AIM AND OBJECTIVES
The aim of the South African Biological Reserve for Small Stock is to promote the improvement and conservation of
South African sheep and goat breeds.
The objectives of this program are to:
• Maintain resource flocks of various small stock breeds as reference populations and source of phenotypic data
and genetic material in collaboration with provincial departments of agriculture and breeders
• Collect blood samples from animals in the reference flocks, store blood samples, extract and store DNA in
suitable minus 80 °C storage facilities
• Collect embryos, semen and somatic cell tissue samples from endangered breeds and store these in liquid
nitrogen storage facilities
• Develop and maintain a database with all relevant genetic, production and reproduction data
• Provide biological material and data to South African research institutions for the promotion of genomic
research on the improvement of the sheep and goat population of the country
• Conserve and preserve the genetic diversity of South African sheep and goat breeds
• Conserve and preserve the indigenous sheep and goat breeds of South Africa.
BACKGROUND
The South African Biological Reserve for Small Stock (GADI-Biobank) was established at the Grootfontein
Agricultural Development Institute with the aim to promote and facilitate the improvement and conservation of South
African sheep and goat breeds. The layout of this program is summarised in Table 1.
The three projects (AP10/1, AP10/2 and AP10/3) respectively deal with the establishment and maintenance of:
• Live flocks of animals (conservation and research)
• Cryopreservation bank (primarily conservation, secondary research)
• Blood and DNA bank (genomic research).
ACTIVITIES DURING REPORT YEAR
Current projects and sub-projects
AP10/1: Live flocks of animals
This project involves the maintenance of various flocks as resource for the Biobank, as well as for other research work.
Currently there are five sub-projects running under this project, namely for the Angora goats, Namaqua Afrikaner,
Merino, Dohne Merino and Afrino sheep.
AP10/2: Cryopreservation bank
Due to budget constraints, no embryos were cryopreserved during this report year. The total number of frozen embryos
in the bank is 307.
AP10/3: Blood and DNA bank
Various projects for breeds participating in the blood and DNA bank project, namely Afrino, Merino, Dohne Merino,
Namaqua Afrikaner and Meatmaster sheep and Angora goats, are underway.
Policy and ownership of samples
The following documents relating to the operation of the GADI-Biobank are used:
• Policy for GADI-Biobank
• Transfer of Biological Material to GADI-Biobank
• Agreement for the Supply of Resource Material.
34
Table 1. Layout of the program
PROGRAM AP10
Establishment of the South African Biological Reserve for Small Stock research and conservation
PROJECT AP10/1
Establishment and maintenance of
live flocks of sheep and goat breeds
in South Africa
PROJECT AP10/2
Cryopreservation bank for
conservation of biodiversity of sheep
and goat breeds in South Africa
PROJECT AP10/3
Blood and DNA bank for genomic
research in sheep and goat breeds in
South Africa
SUB-PROJECTS SUB-PROJECTS SUB-PROJECTS
AP10/1/1: Establishment and
maintenance of live flocks of the
endangered Namaqua Afrikaner
sheep breed in South Africa
AP10/2/1: Establishment and
maintenance of a cryopreservation
bank for Namaqua Afrikaner sheep
AP10/3/1: Maintenance of a
biological bank for Angora goats in
South Africa
AP10/1/2: Maintenance of live flocks
of Angora goats as reference flocks
for a biological bank for Angora
goats in South Africa (Completed)
AP10/2/1/1: Characterisation and
cryopreservation of semen from the
indigenous Namaqua Afrikaner
sheep breed, in comparison with the
Dorper and Dohne Merino breeds
(Completed)
AP10/3/1/1: Maintenance of a
biological bank for Angora goats in
South Africa: Grootfontein Student
Angora Stud
AP10/1/3: Maintenance of two
Merino flocks as resource flocks for
research and reference flocks for a
biological bank for Merino sheep in
South Africa
AP10/2/1/2: Intensive rearing of
Namaqua Afrikaner lambs from
weaning until breeding age for use in
semen freezing protocol trials
AP10/3/2: Maintenance of a
biological bank for Namaqua
Afrikaner sheep in South Africa
AP10/1/4: Maintenance of an Afrino
flock as resource for research and as
reference flock for a biological bank
for Afrino sheep in South Africa
AP10/3/3: Maintenance of a
biological bank for Merino sheep in
South Africa
AP10/1/5: Maintenance of an Angora
goat resource flock at Grootfontein
Agricultural Development Institute
AP10/3/4: Maintenance of a
biological bank for Afrino sheep in
South Africa
AP10/1/6: Maintenance of a Dohne
Merino flock as resource for research
and as reference flock for a
biological bank for Dohne Merino
sheep in South Africa
AP10/3/6: Maintenance of a
biological bank for Dohne Merino
sheep in South Africa
AP10/3/7: Maintenance of a
biological bank for Meatmaster
sheep in South Africa
CONCLUDING REMARKS
The program is running according to schedule and project activities will continue as stipulated in the project protocols.
Summary of activities performed during the 2018/2019 reporting year:
• Five sub-projects are underway under the “Maintenance of live flocks”-project. These involve five sheep and
one Angora goat flocks. All phenotypic data recorded have been entered into the database
• To date, 307 Namaqua Afrikaner embryos have been cryopreserved and are being stored in the cryopreservation
bank
• Blood samples from 56 730 Angora goats and sheep have been collected and stored in the blood and DNA bank
• Researchers from six research institutions already made use of samples and data from the blood and DNA bank
for various research projects.
ACKNOWLEDGEMENTS
The following people are acknowledged for their contribution to this program:
• Technicians at experimental stations for collection of data
• Participating breeders for their inputs
• Mohair South Africa for partial funding of the Angora goat DNA bank project
• Cape Wools for partial funding of the Merino sheep DNA bank project
• Eastern Cape Department of Rural Development and Agrarian Reform
• Northern Cape Department of Agriculture, Land Reform and Rural Development.
35
Establishment and maintenance of live flocks of the endangered Namaqua Afrikaner sheep
breed in South Africa
M.A. Snyman
AIM AND OBJECTIVES
The aim of this project is to conserve and preserve the endangered, indigenous Namaqua Afrikaner sheep breed in
South Africa via an in situ conservation program.
The objectives of this project are to:
• Maintain the Namaqua Afrikaner flocks at the Carnarvon and Karakul Experimental Stations
• Locate current breeders/owners of Namaqua Afrikaner sheep
• Identify private farms for establishment of live flocks of Namaqua Afrikaner sheep
• Maintain these flocks
• Collect pedigree and phenotypic data on animals in the flocks
• Make these resources available for inclusion in the blood, DNA and cryopreservation biobanks.
BACKGROUND
The Northern Cape Department of Agriculture, Land Reform and Rural Development maintains two Namaqua
Afrikaner flocks at two of its experimental stations near the towns of Carnarvon and Upington in the Northern Cape
Province. These flocks are kept for the purpose of the preservation of this genetic pool and the collection of production
and reproduction data on this breed. This report deals with the data collected on the Carnarvon Namaqua Afrikaner
flock.
This project also supplies animals and performance data resources for the following projects:
• AP2/23: Prediction of tail weight from tail measurements in Namaqua Afrikaner sheep at various ages
• AP10/2/1/2: Intensive rearing of Namaqua Afrikaner lambs from weaning until breeding age for use in semen
freezing protocol trials
• AP10/3/2: Maintenance of a biological bank for the endangered Namaqua Afrikaner sheep breed in Southern
Africa.
RESULTS AND DISCUSSION
Rainfall and veld conditions
The long-term average yearly rainfall for the experimental station and the yearly recorded rainfall since 1991 are
displayed in Figure 1. Since 2013, below average rainfall has been recorded. In 2018, 206 mm rain was recorded.
Although this is average for the region, 178 mm of the rain fell from January until May 2018. For the ensuing period
until December 2019, only 72 mm rain was recorded. The lowest rainfall since 2003 was recorded during 2019 (44
mm), with only 11 mm of rain recorded from May until December 2019.
0
50
100
150
200
250
300
350
400
450
19
91
19
93
19
95
19
97
19
99
20
01
20
03
20
05
20
07
20
09
20
11
20
13
20
15
20
17
20
19
Rain
fall
(m
m)
Year
Annual Long term
Figure 1. Long term average yearly rainfall for the experimental station and yearly recorded rainfall since 1991
36
This resulted in very poor veld conditions which necessitated the provision of supplementary feeding to the Afrino
ewes during mating in April 2019 for the first time in 30 years. The Namaqua Afrikaner ewes did not receive any
supplementation during mating. However, supplementation of the Namaqua ewes commenced during lambing in
September 2019. The ewes received chocolate maize (300 g/ewe/day) and lucerne pellets (300 g/ewe/day) from
September until the end of December 2019. Lucerne hay was provided when available and necessary. This
supplementation was given on a per ewe basis and included the lambs which were run with the ewes until weaning in
January 2020. During January, the supplementation was reduced to 150 g/ewe/day of chocolate maize.
Productive performance
The average body weight of the ram and ewe lambs since 1993 are summarised in Table 1. The description of the
morphological traits recorded on the 2007- to 2018-born lambs is presented in Table 2. The morphometric traits
indicated that rams had bigger body dimensions than ewes, as is evident from the higher body length, wither height and
heart girth. Rams also had longer and thicker tails than ewes (P <0.05). In the majority of the animals, the tails twisted
to the left, while more animals had black heads than brown heads. All rams were horned, except one 2011-born and
one 2018-born ram, which were polled. The majority of ewes also had horns (83.2%). The majority of the animals had
no colour on the body, although this could be expected, as it was one of the criteria on which surplus young animals
were culled.
Table 1. Average productive performance (± s.e.) since 1993 of the ram and ewe lambs in the Carnarvon Namaqua
Afrikaner flock
Trait Rams Ewes
Birth weight (kg) 4.40 ± 0.05 4.15 ± 0.05
42-day body weight (kg) 15.4 ± 0.2 14.4 ± 0.2
120-day weaning weight (kg) 28.0 ± 0.3 26.3 ± 0.3
5-month body weight (kg) 32.3 ± 0.5 29.7 ± 0.5
6-month body weight (kg) 36.4 ± 0.5 32.9 ± 0.5
7-month body weight (kg) 39.0 ± 0.5 35.3 ± 0.5
8-month body weight (kg) 41.6 ± 0.5 37.1 ± 0.5
9-month body weight (kg) 44.9 ± 0.6 38.8 ± 0.6
10-month body weight (kg) 47.4 ± 0.6 40.8 ± 0.6
11-month body weight (kg) 50.4 ± 0.6 42.3 ± 0.6
12-month body weight (kg) 53.7 ± 0.7 44.8 ± 0.6
Table 2. Morphological traits (± s.e.) at 14 months of age of the 2007- to 2018-born Namaqua Afrikaner ewe and ram
lambs in the Carnarvon flock
Trait Rams Ewes
Body length (cm) 74.6a ± 0.4 72.0b ± 0.4
Wither height (cm) 72.2a ± 1.6 69.0b ± 1.6
Heart girth (cm) 100.9a ± 3.0 95.3b ± 3.1
Cannon bone length (cm) 17.7a ± 0.4 17.1b ± 0.4
Tail circumference at base (cm) 47.0a ± 1.4 35.2b ± 1.4
Tail length (cm) 37.3a ± 0.6 36.0b ± 0.6
Testis circumference (cm) 32.3 ± 0.4
Teat length left (mm) 20.1 ± 0.8
Teat length right (mm) 21.0 ± 0.8
Percentage of animals
Tail twist: To Left 63.7 61.7
Tail twist: To Right 33.4 30.2
Tail no twist - straight 2.9 8.1
Colour head: Black 55.9 56.1
Colour head: Brown 40.5 40.4
Colour head: Mixed 3.6 3.5
Colour on body: Yes 23.3 23.0
Colour on body: No 76.7 77.0
Horns 99.8 83.2
Polled 0.2 16.8 a,b Values with different superscripts differ significantly (P <0.05) between sexes
37
The average reproductive performance of the Namaqua Afrikaner ewe flock from 1982 to 2019 is presented in Table 3,
while the reproductive performance of the 2016, 2017, 2018 and 2019 lambing seasons are summarised in Table 4.
Table 3. Body weight (± s.e.) and reproduction (CV %) of Namaqua Afrikaner ewes since 1982 in the Carnarvon flock
Trait Average
Body weight before mating (kg) 51.0 ± 0.7
Body weight after weaning (kg) 50.7 ± 0.9
Reproduction
Total weight of lamb weaned / year (kg) 33.3 (42.9)
Number of lambs born / year 1.39 (40.3)
Number of lambs weaned / year 1.24 (44.5)
Number of lifetime lambing opportunities 3.07
Total weight of lamb weaned / lifetime (kg) 108.6 (37.7)
Number of lambs born / lifetime 4.44 (35.6)
Number of lambs weaned / lifetime 4.00 (38.7)
Table 4. Reproduction of Namaqua Afrikaner ewes from the 2016 until the 2019 lambing seasons
Trait 2016 2017 2018 2019
Body weight before mating (kg) 59.1 53.8 48.8 50.0
Body weight after weaning (kg) - 49.2 - 45.4
Body weight loss: mating to weaning (kg) - 4.6 - 4.6
Number of ewes mated 105 107 105 105
Ewes lambed / 100 ewes mated 77.0 97.2 92.3 82.9
Ewes aborted / 100 ewes mated 0.9 0.9 0 0.95
Lambs born / 100 ewes lambed 169.8 165.4 175.2 146.0
Lambs born / 100 ewes mated 128.6 160.7 161.9 121.0
Stillborn lambs (%) 2.9 5.8 1.8 2.36
Lamb survival rate (%) 97.0 92.0 94.0 88.6
Lambs weaned / 100 ewes mated 120.0 139.2 149.5 103.8
Total weight of lamb weaned (kg) 29.8 28.6 37.7 20.9
Individual weaning weight of lambs (kg) 25.0 20.6 25.0 20.9
Despite the very dry conditions in 2019 and the fact that the Namaqua Afrikaner ewes only started to receive
supplementation during lambing, they did not lose more weight from mating until after weaning of their lambs than
during the 2017 season. Unfortunately, after-weaning weights were not recorded during 2016 and 2018. Only three of
the ewes did not lamb in 2017 with a resultant conception rate of 97.2%. This high conception rate, together with the
high fecundity, contributed to the high weaning percentage, despite the lower lamb survival rate than in 2016. The
higher fecundity recorded in 2018, compared to 2017, contributed to the higher weaning percentage. The latter, in turn,
contributed to the higher total weight of lamb weaned in 2018. A 10% lower conception rate was recorded in 2019 than
in 2018. This, as well as the lower fecundity and lamb survival rates, could be attributed to the poor veld conditions
due to the low rainfall. The lowest percentage of lambs weaned per ewes mated in many years was recorded during the
2019 lambing season.
2020 Breeding season
Due to the drought and poor veld conditions at the experimental station, it was decided not to mate the Namaqua ewes
during the April 2020 breeding season. This proved to be a blessing in disguise as the country went into lockdown due
to the COVID-19 pandemic on 27 March 2020. A further consequence of the lockdown was that no monthly body
weights of the 2019-born Namaqua lambs could be taken during April and May 2020.
38
ESTABLISHMENT AND IDENTIFICATION OF PRIVATELY OWNED FLOCKS
Three private owners received Namaqua Afrikaner ewes and rams during the reporting period (Table 5).
Table 5. Private owners that obtained Namaqua Afrikaners from Carnarvon Experimental Station during 2019/2020
Owner Farm, District Number of animals received from Carnarvon
Ewes Rams
N.D. Selao Klaarkom, Kuruman 2
J. Claasens Weltevrede, Prince Albert 15 1
B. Steenkamp Klipbanksfontein, Carnarvon 37 19
Total 52 22
PUBLICATIONS
The following have already been published from this project:
Qwabe, S.O., 2011. Genetic and phenotypic characterisation of the South African Namaqua Afrikaner sheep breed.
MSc thesis, University of Pretoria, Pretoria, South Africa.
Snyman, M.A., Van Marle-Köster, E., Qwabe, S.O. & Visser, C., 2013. Genetic and phenotypic profile of three South
African Namaqua Afrikaner sheep flocks. Grootfontein Agric. 13(1), 5-20.
Qwabe, S.O., Van Marle-Köster, E., Visser, C. & Snyman, M.A., 2013. Case study: Saving the endangered Namaqua
Afrikaner sheep breed through conservation and utilization. FAO special report on Case studies on the
application of biotechnologies for smallholders.
Letsoalo, P.T., Kilian, E., Baca, A., Olivier, H.I.P., Snyman, M.A. & Muchenje, V., 2016. Characterisation and
cryopreservation of semen of the indigenous Namaqua Afrikaner sheep breed. Proceedings of the 49th Congress
of the South African Society of Animal Science, Stellenbosch, 3-6 July.
Letsoalo, P.T., 2017. Characterisation and cryopreservation of semen from the indigenous Namaqua Afrikaner sheep
breed, in comparison with the Dorper and Dohne Merino breeds. MSc thesis, University of Fort Hare, Alice,
South Africa.
Letsoalo, P.T., Snyman, M.A., Baca, A. & Muchenje, V., 2018. Characterisation and cryopreservation of semen from
the indigenous Namaqua Afrikaner sheep breed, in comparison with the Dorper and Dohne Merino breeds.
Grootfontein Agric 18(1), 20-32.
CONCLUDING REMARKS
The impact of the drought on the project due to the fact that the ewes were not mated during the 2020 breeding season,
can only be evaluated in four or five years’ time.
ACKNOWLEDGEMENTS
The following people / institutions are acknowledged for their contribution to this project:
• Northern Cape Department of Agriculture, Land Reform and Rural Development
• Personnel at the Carnarvon Experimental Station for data collection and maintenance of the flock
• Personnel at GADI for data collection
• Participating private owners of Namaqua Afrikaner sheep.
39
Maintenance of two Merino flocks as resource flocks for research and reference flocks for a
biological bank for Merino sheep in South Africa
W.J. Olivier
AIM AND OBJECTIVES
The aim of this project is to maintain two Merino flocks as resource for research and reference flocks for a biological
bank for Merino sheep in South Africa.
The objectives of this project are to:
• Maintain the current Merino flocks at GADI and Cradock Experimental Station
• Collect production and reproduction data on all animals in the participating flocks
• Store blood samples and extracted DNA samples of all animals
• Create and maintain a database with all relevant genetic, production and reproduction data
• Make these resources available for qualifying researchers in South Africa for genomic and other research
studies or projects
• Make animals available for student and farmer training.
BACKGROUND
Two Merino flocks are part of the research program of GADI. The Cradock fine wool Merino stud (CMS) is kept
under intensive conditions on irrigated pastures at Cradock Experimental Station, while the Grootfontein Merino stud
(GMS) is kept under extensive conditions on natural pastures at GADI. Both these flocks have been part of long-term
selection experiments since their establishment.
The combined structure and ewe flock size of the two Merino flocks mentioned above make them suitable as a
reference population for a biological bank. Furthermore, the genetic links between these two flocks are very strong and
make it suitable for the investigation of genotype or sire by environmental interactions. The data sets collected on these
research flocks are of the most comprehensive data sets on productive and reproductive traits of Merino sheep
available worldwide. Numerous scientific articles, employing the latest technology at the time, have been published on
data collected on these flocks. It is therefore imperative that this genetic material should be maintained as resource for
future research in quantitative genetics, genetic diversity studies and genomic studies in Merino sheep. It could
furthermore play an important role in the conservation of biodiversity in the South African small stock industry.
This flock is currently also part of the following research projects:
• AP1/17/1: Quantification of the genetic relationship between reproduction and body weight in different sheep
flocks
• AP1/17/2: Genome-wide association study to identify possible genetic markers (SNPs) associated with
reproduction and body weight in different sheep flocks
• AP1/17/4: Identification of genomic regions associated with body weight and reproduction in two South
African sheep breeds
• AP2/20: Establishment of a reference population for future implementation of genomic breeding values for
the South African Merino sheep breed
• AP10/3/3: Maintenance of a biological bank for Merino sheep in South Africa.
RESULTS AND DISCUSSION
The birth coat score, birth weight, 42-day weight, weaning weight and 6-month body weight of the 2019 lambs born in
the respective flocks are presented in Table 1. Due to the COVID-19 lockdown the 6-month body weight of the GMS
lambs was not recorded.
Table 1. Birth coat score and body weights (± s.e.) of the 2019 progeny
Trait Cradock Grootfontein
Ram lambs Ewe lambs Ram lambs Ewe lambs
Birth coat score 1.1 ± 0.1 1.2 ± 0.1 2.3 ± 0.1 2.3 ± 0.1
Birth weight (kg) 4.6 ± 0.5 4.9 ± 0.5 3.9 ± 0.1 3.9 ± 0.1
42-day weight (kg) 12.6 ± 0.4 12.1 ± 0.4 18.1 ± 0.9 17.5 ± 0.9
Weaning weight (kg) 23.8 ± 1.2 22.6 ± 1.2 30.0 ± 1.7 28.1 ± 1.6
6-month weight (kg) 32.4 ± 1.7 30.7 ± 1.7 - -
40
The 12-month and 16-month body weights of the lambs born during September (GMS) and October (CMS) 2018 are
presented in Table 2. The 12-month body weight was corrected for age, while the 16-month body weight used was the
corrected weight as received from the Small Stock Improvement Scheme. The fixed effects included in the final
models were sex, rearing status and age of the dam in years.
Table 2. The body weights (± s.e.) of the 2018-born progeny
Trait Cradock Grootfontein
Ram lambs
12-month body weight (kg) 64.2 ± 1.9 42.5 ± 1.3
16-month body weight (kg) 65.9 ± 1.9 45.1 ± 1.3
Ewe lambs
12-month body weight (kg) 55.8 ± 1.9 43.9 ± 1.3
16-month body weight (kg) 53.9 ± 1.9 43.7 ± 1.3
The wool production data at the age of 13 months of the 2018-born ram and ewe progeny are summarised in Table 3
and the subjectively assessed wool and conformation traits and the body dimension measurements are summarised in
Tables 4 and 5 respectively.
Table 3. Wool production data (± s.e.) of the 2018-born ram and ewe progeny at selection age
Trait Cradock Grootfontein
Rams Ewes Rams Ewes
12-month fibre diameter (μm) 16.4 ± 0.2 16.7 ± 0.2 14.9 ± 0.2 16.2 ± 0.2
16-month fibre diameter (μm) 16.9 ± 0.3 17.7 ± 0.3 15.3 ± 0.2 16.8 ± 0.2
Greasy fleece weight (kg) 5.9 ± 0.3 5.5 ± 0.3 4.2 ± 0.2 4.3 ± 0.2
Clean fleece weight (kg) 3.6 ± 0.2 3.5 ± 0.2 2.6 ± 0.1 2.8 ± 0.1
Clean yield (%) 60.7 ± 1.4 63.4 ± 1.4 62.7 ± 1.5 65.5 ± 1.6
Staple length (mm) 80.7 ± 2.4 87.3 ± 2.5 97.2 ± 2.6 106.1 ± 2.8
Pleat score (n) 6.5 ± 0.2 6.4 ± 0.2 6.3 ± 0.2 6.5 ± 0.2
Number of crimps per 25 mm 13.5 ± 0.6 13.7 ± 0.6 11.9 ± 0.4 12.9 ± 0.4
Duerden 86.1 ± 1.9 90.6 ± 2.0 74.2 ± 1.4 83.5 ± 1.5
Coefficient of variation (%) 14.9 ± 0.5 13.7 ± 0.5 17.1 ± 0.6 15.6 ± 0.6
Comfort factor (%) 99.8 ± 0.0 99.8 ± 0.0 99.9 ± 0.0 99.8 ± 0.0
Staple strength (N/Ktex) 39.6 ± 2.4 56.2 ± 2.4 46.6 ± 2.6 51.8 ± 2.6
Table 4. The subjective wool and conformation traits (± s.e.) of the 2018-born ram and ewe progeny at selection age
Trait Cradock Grootfontein
Rams Ewes Rams Ewes
Wool quality 20.0 ± 2.2 23.2 ± 2.2 33.5 ± 1.0 34.1 ± 1.1
Variation over the fleece 21.1 ± 2.1 25.0 ± 2.2 33.7 ± 1.1 34.7 ± 1.1
Wool yolk 18.3 ± 1.5 19.2 ± 1.6 24.4 ± 0.7 24.8 ± 0.8
Staple formation 19.7 ± 2.0 21.9 ± 2.0 19.6 ± 1.3 20.4 ± 1.4
Bellies and points 22.5 ± 3.2 21.2 ± 3.2 26.0 ± 1.0 26.4 ± 1.1
Wool colour 26.4 ± 2.0 32.0 ± 2.1 29.6 ± 1.7 29.5 ± 1.8
Conformation of the head 24.6 ± 2.8 25.1 ± 2.8 32.0 ± 0.9 32.5 ± 1.0
Colour 27.6 ± 2.4 28.7 ± 2.4 23.8 ± 1.3 26.7 ± 1.3
Pasterns 33.6 ± 1.5 36.7 ± 1.5 30.3 ± 0.9 30.0 ± 0.9
Hocks 23.3 ± 1.5 21.5 ± 1.5 16.5 ± 1.3 20.1 ± 1.3
Front quarters 23.8 ± 1.5 23.6 ± 1.5 17.0 ± 0.9 19.6 ± 0.9
Overall conformation 24.5 ± 1.7 23.9 ± 1.8 16.6 ± 1.5 23.1 ± 1.7
It is evident from Table 4 that the scores for staple formation, hocks, front quarters and overall conformation of GMS were
below average, while for CMS, wool quality, variation over the fleece, staple formation and wool yolk were below average.
41
Table 5. Body dimension measurements (± s.e.) of the 2018-born progeny at selection age
Trait Cradock Grootfontein
Rams Ewes Rams Ewes
Body length (cm) 87.0 ± 1.2 85.2 ± 1.2 75.3 ± 1.1 74.1 ± 1.2
Body depth (cm) 76.7 ± 1.2 73.8 ± 1.2 72.5 ± 0.8 71.0 ± 0.9
Front cannon bone length (cm) 15.1 ± 0.5 15.3 ± 0.5 15.5 ± 0.5 15.4 ± 0.5
Heart girth (cm) 100.3 ± 1.6 100.1 ± 1.6 83.0 ± 2.3 82.6 ± 2.4
Horn length (cm) 33.5 ± 1.8 16.2 ± 2.0 26.7 ± 1.1 15.8 ± 1.3
Horn base circumference (cm) 22.7 ± 0.1 11.5 ± 0.1 19.8 ± 0.7 11.8 ± 0.7
Length of the left teat (mm) - 22.6 ± 2.1 - 21.5 ± 2.1
Length of the right teat (mm) - 22.6 ± 2.1 - 21.2 ± 2.1
Testis circumference (cm) 36.7 ± 2.0 - 29.5 ± 2.0 -
Testis length (cm) 16.5 ± 1.4 - 15.3 ± 1.3 -
The information of the 2019 breeding season for both studs is summarised in Table 6. The low conception rate of the
Cradock fine wool Merino stud (CMS) could possibly be ascribed to the fact that CMS is infected with Ovine Johne’s
Disease. The poor survival rate in the Grootfontein Merino stud (GMS) is a combined effect of the poor environmental
conditions during 2019, as well as problems with stray dogs that killed 15 lambs.
Table 6. Reproduction data of the 2019 breeding season
Trait Cradock Grootfontein
Number of ewes mated 209 199
Mating weight of adult ewes (kg) 67.8 ± 0.7 55.9 ± 0.9
Mating weight of young ewes (kg) 58.5 ± 1.6 54.5 ± 0.4
Conception rate (number of ewes that lambed / number of ewes mated) 76.1 94.0
Lambing percentage (number of lambs born / number of ewes mated) 132.1 133.2
Weaning percentage (number of lambs weaned / number of ewes mated) 90.9 83.9
Mortality of lambs:
Died between birth and 42 days (%) 25.7 25.7
Died between 42 days and weaning (%) 5.4 11.3
Died between birth and weaning (%) 31.2 37.0
Total weight of lamb weaned per adult ewe (kg) 17.3 ± 3.3 23.7 ± 1.3
Total weight of lamb weaned per young ewe (kg) 20.8 ± 1.4 17.6 ± 2.8
Due to the COVID-19 lockdown the wool samples from the Cradock Merino stud could not be analysed, while the
Grootfontein Merino stud ewes were not shorn before mating. The Grootfontein ewes will be shorn during mid-
pregnancy.
PUBLICATIONS
The following have already been published from this project:
Olivier, W.J., 2013. The evaluation of a South African fine wool genetic resource flock. PhD thesis, University of
Stellenbosch, Stellenbosch, South Africa.
Nemutandani, K.R., Snyman, M.A., Olivier, W.J. & Visser, C., 2014. Genetic analysis of body weight at different ages
in the Grootfontein Merino stud. Proceedings of the 47th Congress of the South African Society of Animal Science,
Pretoria, 6 - 8 July, 91.
Nemutandani, K.R., Snyman, M.A., Olivier, W.J. & Visser, C., 2016. Comparison of breeding values for body weight
in Merino sheep estimated with different statistical procedures. Proceedings of the 49th Congress of the South
African Society of Animal Science, Stellenbosch, 4-7 July, 57.
Nemutandani, K.R., Snyman, M.A., Olivier, W.J. & Visser, C., 2016. (Co)variance components and genetic
parameters estimation using a repeatability model in the Grootfontein Merino stud. Proceedings of the 49th
Congress of the South African Society of Animal Science, Stellenbosch, 4-7 July, 193.
Olivier, W.J. & Snyman, M.A., 2016. Population structure and pedigree analysis of the Grootfontein Dohne Merino
stud. Proceedings of the 49th Congress of the South African Society of Animal Science, Stellenbosch, 4-7 July, 199.
42
Olivier, W.J. & Van Graan, A.C., 2016. Evaluation of birth coat score as a possible early selection indicator for wool
characteristics. Proceedings of the 49th Congress of the South African Society of Animal Science, Stellenbosch, 4-7
July, 43.
Olivier, W.J., 2016. The effect of culling lambs at weaning on estimated breeding values of performance data of a
Merino stud. Proceedings of the 49th Congress of the South African Society of Animal Science, Stellenbosch, 4-7
July, 64.
Nemutandani, K.R., Olivier, W.J., Snyman, M.A. & Visser, C., 2017. Estimation of direct and maternal effects on
body weight in Merino sheep using random regression models. Proceedings of the 50th Congress of the South
African Society of Animal Science, Port Elizabeth, 18 - 21 September.
Nemutandani, K.R., Snyman, M.A., Olivier, W.J. & Visser, C., 2018. Estimation of variance components and
heritabilities for body weight from birth to six years of age in Merino sheep using random regression models.
Proceedings of the 11th World Congress on Genetics Applied to Livestock Production, Auckland, New Zealand, 11-
16 February.
Nemutandani, K.R., 2018. Genetic analysis of body weight at different ages in the Grootfontein Merino stud.
MScAgric thesis, University of Pretoria, Pretoria, South Africa.
Nemutandani, K.R., Snyman, M.A., Olivier, W.J. & Visser, C., 2018. Estimation of genetic parameters and
comparison of breeding values for body weight with different models in a South African Merino stud. Small
Ruminant Research 169, 34-41.
Olivier, W.J., 2018. The effect of culling lambs at weaning on estimated breeding values of performance traits at 15
months of age in a Merino stud. Grootfontein Agric 18, 33-39.
CONCLUDING REMARKS
All the production and reproduction data were recorded and stored during the reporting period.
ACKNOWLEDGEMENTS
The following people / institutions are acknowledged for their contribution to this project:
• Eastern Cape Department of Rural Development and Agrarian Reform
• Personnel at the Cradock Experimental Station and GADI for data collection and maintenance of the flocks
• Officials from BKB for classing of the animals
• Cape Wools SA for partial funding of the project.
43
Maintenance of an Afrino flock as resource for research and as reference flock for a
biological bank for Afrino sheep in South Africa
M.A. Snyman
AIM AND OBJECTIVES
The aim of this project is to maintain an Afrino flock as resource for research and a reference flock for a biological
bank for Afrino sheep in South Africa.
The objectives of this project are to:
• Maintain the current Afrino flock at the Carnarvon Experimental Station
• Evaluate selection criteria to improve reproductive efficiency, mutton and wool production of dual purpose
sheep breeds under extensive grazing conditions
• Collect production and reproduction data on all animals in the flock and create and maintain a database with all
relevant genetic, production and reproduction data for dual purpose sheep in South Africa
• Store blood samples and extracted DNA samples of all animals
• Make these resources available for qualifying researchers in South Africa for genomic and other research
studies or projects
• Provide research animals for other projects.
BACKGROUND
This is a co-operative project between the Northern Cape Department of Agriculture, Land Reform and Rural
Development and Grootfontein Agricultural Development Institute. The project is continuing as in the past.
Researchers and technicians from GADI are still responsible for data capturing, linear scoring of subjective traits and
selection of breeding sires and dams. This is done in collaboration with the farm personnel at Carnarvon Experimental
Station, who are responsible for data collection and maintenance of the flock.
This flock is currently also part of the following research projects:
• AP1/17/1: Quantification of the genetic relationship between reproduction and body weight in different sheep
flocks
• AP1/17/2: Genome-wide association study to identify possible genetic markers (SNPs) associated with
reproduction and body weight in different sheep flocks
• AP1/17/4: Identification of genomic regions associated with body weight and reproduction in two South
African sheep breeds
• AP10/3/4: Maintenance of a biological bank for Afrino sheep in South Africa.
RESULTS AND DISCUSSION
Rainfall and veld conditions
Long term average yearly rainfall recorded for the experimental station and the yearly recorded rainfall since 1991 are
illustrated in Figure 1. Since 2013, below average rainfall has been recorded. In 2018, 206 mm rain was recorded.
Although this is average for the region, 178 mm of the rain fell from January until May 2018. For the ensuing period
until December 2019, only 72 mm rain was recorded. The lowest rainfall since 2003 was recorded during 2019 (44
mm), with only 11 mm of rain recorded from May until December 2019.
0
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150
200
250
300
350
400
450
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Figure 1. Long term average yearly rainfall for the experimental station and yearly recorded rainfall since 1991
44
This resulted in very poor veld conditions which necessitated the provision of supplementary feeding to the Afrino
ewes during mating in April 2019 for the first time in 30 years. No supplementation was provided during pregnancy,
but supplementation of the Afrino ewes commenced during lambing in September 2019. The ewes received chocolate
maize (350 g/ewe/day) and lucerne pellets (350 g/ewe/day) from September until the end of December 2019. Lucerne
hay was provided when available and necessary. This supplementation was given on a per ewe basis and included the
lambs which were run with the ewes until weaning in January 2020. During January, the supplementation was reduced
to 220 g/ewe/day of chocolate maize.
Production and reproduction
The average productive performance and subjectively assessed traits of the ram and ewe lambs since 1990 are
summarised in Tables 1 and 2 respectively.
Table 1. Average productive performance (± s.e.) since 1990 of ram and ewe lambs in the Carnarvon Afrino flock
Trait Rams Ewes
Birth weight (kg) 4.90 ± 0.01 4.63 ± 0.01
42-day body weight (kg) 16.0 ± 0.2 15.0 ± 0.2
120-day weaning weight (kg) 32.4 ± 0.2 30.0 ± 0.2
5-month body weight (kg) 33.6 ± 0.4 30.5 ± 0.4
6-month body weight (kg) 38.2 ± 0.4 34.9 ± 0.4
7-month body weight (kg) 40.9 ± 0.4 37.3 ± 0.4
8-month body weight (kg) 45.6 ± 0.4 40.7 ± 0.4
9-month body weight (kg) 49.6 ± 0.4 43.8 ± 0.4
10-month body weight (kg) 53.2 ± 0.5 46.9 ± 0.5
11-month body weight (kg) 56.6 ± 0.5 49.3 ± 0.5
12-month body weight (kg) 60.9 ± 0.5 52.9 ± 0.5
14-month body weight (kg) 64.3 ± 0.5 53.2 ± 0.5
Greasy fleece weight (kg) 3.24 ± 0.05 3.03 ± 0.05
Clean fleece weight (kg) 2.05 ± 0.04 1.98 ± 0.04
Fibre diameter (µm) 19.4 ± 0.1 19.8 ± 0.1
Clean yield (%) 61.1 ± 0.6 62.3 ± 0.6
Staple length (mm) 83.2 ± 1.0 86.1 ± 1.0
Number of crimps/25 mm 17.9 ± 1.3 17.2 ± 134
Coefficient of variation (%) 16.6 ± 0.2 16.6 ± 0.2
Standard deviation (µm) 3.15 ± 0.04 3.23 ± 0.04
Comfort factor (%) 99.5 ± 0.1 99.3 ± 0.1
Staple strength (N/Ktex) 35.8 ± 1.3 35.5 ± 1.3
Table 2. Average scores for subjectively assessed wool and conformation traits (± s.e.) at 14 months of age since 1990
of ram and ewe lambs in the Carnarvon Afrino flock
Trait Rams Ewes
Conformation of the head 32.6 ± 1.2 33.0 ± 1.2
Softness of face cover 33.0 ± 0.9 33.4 ± 0.9
Pigmentation 26.1 ± 1.4 27.0 ± 1.4
Front quarters 33.4 ± 0.8 32.7 ± 0.8
Front pasterns 36.1 ± 0.8 36.9 ± 0.8
Hind pasterns 36.5 ± 0.7 37.1 ± 0.7
Hocks 34.8 ± 1.0 34.6 ± 1.0
Top line 34.9 ± 0.7 35.9 ± 0.7
Body length (cm) 78.5 ± 0.6 75.5 ± 0.6
Wither height (cm) 70.2 ± 0.6 67.6 ± 0.6
Heart girth (cm) 103.7 ± 2.5 99.5 ± 2.5
Front cannon bone length (cm) 18.4 ± 0.3 17.6 ± 0.3
Softness of fleece 32.5 ± 1.1 32.0 ± 1.1
Crimp definition 29.8 ± 1.4 30.7 ± 1.4
Uniformity of fleece 35.2 ± 1.0 35.6 ± 1.0
Density of fleece 34.6 ± 0.9 35.2 ± 0.9
Wool colour 32.3 ± 0.8 32.9 ± 0.8
45
Trait Rams Ewes
Creeping belly 33.2 ± 1.7 35.4 ± 1.7
Scrotal circumference (cm) 33.9 ± 0.5
Teat length left (mm) 23.7 ± 0.9
Teat length right (mm) 23.1 ± 0.9
Selection in the flock is aimed at increasing reproductive performance and body weight, maintaining wool weight and
fibre diameter and improving wool quality traits. Genetic trends for body weights, wool traits and reproduction are
summarised in Table 3. It is evident that the selection objectives with regard to reproductive performance, body weight
and most of the wool traits have been achieved.
Table 3. Genetic trends in production and reproduction traits in the Carnarvon Afrino flock since 1990
Trait Genetic trend R2
Birth weight (kg) y = 0.0097x-0.0109 0.8580
Birth weight maternal (kg) y = 0.0021x+0.0183 0.6053
42-day body weight (kg) y = 0.0221x-0.0184 0.8705
42-day body weight maternal (kg) y = 0.0001x+0.1143 0.0003
120-day weaning weight (kg) y = 0.0503x+0.0786 0.9605
120-day weaning weight maternal (kg) y = 0.0181x+0.0430 0.6436
9-month body weight (kg) y = 0.1328x+0.1595 0.9839
16-month body weight (kg) y = 0.3175x-0.0732 0.9832
Clean fleece weight (kg) y = 0.0119x-0.1696 0.7433
Fibre diameter (µm) y = 0.0061x2-0.2151x+0.3623 0.9527
Total weight of lamb weaned (kg) y = 1.5798Ln(x)+6.8348 0.6593
Number of lambs born y = 0.0725Ln(x)+0.3724 0.5417
Number of lambs weaned y = 0.06516Ln(x)+0.2958 0.6038
Productive performance of the ewe flock since 1990 is presented in Table 4, while the reproductive performance of the
2016 to 2019 lambing seasons is summarised in Table 5. The effects of the drought and subsequent poor veld
conditions are evident from the higher loss in body weight of the ewes from mating until after weaning of their lambs
in 2019 than during the 2017 season. Unfortunately, after-weaning weights were not recorded during 2016 and 2018.
The 1.5% lower conception rate and 11.2% lower lamb survival rate recorded in 2017 compared to 2016, contributed
to the 14% lower weaning percentage recorded for the 2017 lambing season. The higher fecundity recorded in 2018,
compared to 2017, contributed to the higher weaning percentage. The latter, as well as the fact that the ewes received
some supplementation during lactation in 2018, contributed to the higher total weight of lamb weaned in 2018. Despite
the drought, the conception percentage in 2019 was higher than in 2018 and in line with the previous years. This could
probably be ascribed to the supplementation received during the 2019 breeding season. The fecundity and weaning
percentage, however, were much lower during 2019. The lowest percentage of lambs weaned per ewes mated in many
years was recorded during the 2019 lambing season.
Table 4. Production (± s.e.) of Afrino ewes since 1990 in the Carnarvon flock
Trait Average
Body weight (kg) 67.6 ± 0.9
Greasy fleece weight (kg) 2.67 ± 0.09
Clean fleece weight (kg) 1.73 ± 0.04
Fibre diameter (µm) 20.6 ± 0.1
Clean yield (%) 64.5 ± 0.6
Staple length (mm) 74.9 ± 1.0
Number of crimps/25 mm 14.0 ± 0.2
Coefficient of variation (%) (since 2000) 17.6 ± 0.2
Standard deviation (µm) (since 2000) 3.39 ± 0.04
Comfort factor (%) (since 2000) 99.3 ± 0.1
Staple strength (N/Ktex) (since 2008) 28.7 ± 0.8
Creeping belly score (since 2004) 30.9 ± 1.2
46
Trait Average
Reproduction
Total weight of lamb weaned / year (kg) 36.59 ± 0.06
Number of lambs born / year 1.34 ± 0.10
Number of lambs weaned / year 1.18 ± 0.05
Number of lambing opportunities 3.32
Total weight of lamb weaned / lifetime (kg) 130.0 ± 2.5
Number of lambs born / lifetime 4.66 ± 0.09
Number of lambs weaned / lifetime 4.18 ± 0.08
Table 5. Reproduction of Afrino ewes from the 2016 until the 2019 lambing seasons
Trait 2016 2017 2018 2019
Body weight before mating (kg) 72.5 71.1 64.8 70.2
Body weight after weaning (kg) - 64.1 - 53.4
Body weight loss mating to weaning (kg) - 7.0 - 16.8
Number of ewes mated 202 203 199 201
Ewes lambed / 100 ewes mated 92.1 90.6 89.4 93.0
Ewes aborted / 100 ewes mated 0.5 0.5 0 0
Lambs born / 100 ewes lambed 147.8 151.1 170.2 140.6
Lambs born / 100 ewes mated 136.1 136.9 152.3 130.8
Stillborn lambs (%) 2.9 3.2 2.97 4.18
Lamb survival rate (%) 97.4 86.2 92.9 80.9
Lambs weaned / 100 ewes mated 128.7 114.3 137.2 101.0
Total weight of lamb weaned (kg) 35.6 32.3 46.7 26.5
Individual weaning weight of lambs (kg) 27.9 28.3 32.9 27.4
PUBLICATIONS
The following have already been published from this project:
Snyman, M.A. & Olivier, W.J., 2015. An analysis of creeping belly in the Carnarvon Afrino sheep flock. Grootfontein
Agric 15(1), 1-9.
Dzomba, E.F., Snyman, M.A., Chimonyo, M. & Muchadeyi, F.C., 2016. P4055 Assessing the genomic status of South
African mutton, pelt and dual purpose sheep breeds using genome-wide single nucleotide genotypes. Journal of
Animal Science 94(4), 106.
Snyman, M.A., Cloete, S.W.P. & Olivier, W.J., 2016. Genetic parameters for milk production of ewes in four South
African woolled sheep flocks. Proceedings of the 49th Congress of the South African Society of Animal
Science, Stellenbosch, 3-6 July.
Snyman, M.A., Cloete, S.W.P. & Olivier, W.J., 2016. Genetic parameters for milk production of ewes in four South
African woolled sheep flocks under different grazing conditions. Grootfontein Agric 16(1), 1-15.
Snyman, M.A. & Olivier, W.J., 2016. Population structure and pedigree analysis of the Carnarvon Afrino flock.
Proceedings of the 49th Congress of the South African Society of Animal Science, Stellenbosch, 3-6 July.
CONCLUDING REMARKS
The impact of the drought on the project due to the fact that the ewes were not mated during the 2020 breeding season,
as well as the earlier recording of selection age data can only be evaluated in four or five years’ time.
ACKNOWLEDGEMENTS
The following people / institutions are acknowledged for their contribution to this project:
• Northern Cape Department of Agriculture, Land Reform and Rural Development
• Personnel at the Carnarvon Experimental Station for data collection and maintenance of the animals
• Personnel at GADI for data collection.
47
Blood and DNA bank for genomic research in sheep and goat breeds in South Africa
M.A. Snyman
AIM AND OBJECTIVES
The aim of this project is to maintain a blood and DNA bank for small stock breeds (sheep and goats) in South Africa
as resource for genomic research.
The objectives of this project are to:
• Maintain and expand the existing central storage facility of the blood and DNA bank for South African small
stock breeds at Grootfontein Agricultural Development Institute (GADI)
• Maintain an operational DNA laboratory for this purpose
• Collect blood samples from all animals in the participating flocks
• Store blood samples of all animals
• Extract and store DNA of sub-samples
• Collect production and reproduction data on all animals in the participating flocks
• Create and maintain a database with all relevant genetic, production and reproduction data
• Make these resources available to qualifying researchers in South Africa for genomic research studies.
BACKGROUND
The blood and DNA bank forms part of the bigger program on the establishment of a South African Biological Reserve
for small stock research and conservation (GADI-Biobank). It serves as a depot for resource material for genomic
research projects. Seven projects for breeds participating in the blood and DNA bank project (Afrino, Merino, Dohne
Merino, Namaqua Afrikaner and Meatmaster sheep and Angora goats) are underway.
The following sheep flocks are part of the DNA and blood bank projects (AP10/3):
• Afrino flock at the Carnarvon Experimental Station (200 ewes)
• Fine wool Merino stud at Cradock Experimental Station (220 ewes)
• Merino stud at Grootfontein Agricultural Development Institute (220 ewes)
• Namaqua Afrikaner flock at the Carnarvon Experimental Station (110 ewes)
• Namaqua Afrikaner flock at the Karakul Experimental Station (120 ewes)
• Namaqua Afrikaner flock at Welgeluk, Mr Johann van der Merwe, Carnarvon (110 ewes)
• Dohne Merino stud at Dohne Agricultural Development Institute (120 ewes)
• Dohne Merino stud at Grootfontein Agricultural Development Institute (400 ewes)
• Dohne Merino stud of Mr Robbie Blaine, Wauldby, Stutterheim (320 ewes)
• Meatmaster stud of Mr Clinton Collett, La Rochelle, Venterstad (350 ewes)
• Merino stud of Mr Eric Naudé, Leopardsvlei, Middelburg (1000 ewes)
• Merino stud of Mr Geoff Kingwill, Grand View, Murraysburg (450 ewes).
The following Angora goat flocks are part of the Angora blood and DNA bank project:
• Jansenville fine hair and crossbred flocks - Jansenville Experimental Station, Jansenville (until 2015)
• Cape Angora Top Tier - Boksfontein, Murraysburg (until 2007)
• Studs 116 & 217 - Mr Arthur Short, Wheatlands, Graaff-Reinet (until 2010)
• Studs 142, 154, 215 & 317 - Mr Ray Hobson, Baroe, Steytlerville (until 2015)
• Stud 248 - Mr Deon Barkhuizen, Rooiklip, Uniondale (until 2011)
• Stud 323 - Grootfontein Student Angora Stud, Grootfontein (since 2012)
• Angela project - Vleikuil, Rietbron (until 2017).
MATERIALS AND METHODS
Blood sample collection and storage
Blood collection during this reporting period could not take place as usual. Firstly, due to two broken down freezers,
there was not enough freezer space to do the collections as usual. The freezers were repaired at the end of February
2020, using surplus funds from other units at GADI. Therefore, blood samples were only collected from the 2019-born
Grootfontein Dohne Merino, Carnarvon Afrino, Carnarvon Namaqua Afrikaner and the La Rochelle Meatmaster lambs
before the COVID-19 outbreak, after which the lockdown prevented any further travelling for blood collections.
Blood samples were collected into 10 ml EDTA vacutainer blood collection tubes. After collection, the blood samples
were divided into four aliquots of 2 ml blood each into cryo-vials. These samples were frozen at minus 80 °C for future
use. The number of sheep and Angora goats sampled to date is summarised in Tables 1 and 2 respectively. Blood
samples from a total of 56 730 animals have been collected and stored to date.
48
Table 1. Number of blood samples collected to date for Afrino, Merino, Namaqua Afrikaner, Dohne Merino and
Meatmaster sheep
Breed Total
Afrino 3701
Merino - Cradock 4151
Merino - GADI 2793
Merino - E. Naude 5037
Merino - G. Kingwill 3069
Namaqua Afrikaner - Carnarvon 1916
Namaqua Afrikaner - Karakul 545
Namaqua Afrikaner - J. van der Merwe 185
Dohne Merino - Dohne ADI 1502
Dohne Merino - GADI 6484
Dohne Merino - Wauldby 1986
Meatmaster 5093
Total 36462
Table 2. Number of blood samples collected to date for Angora goats
Participant Total
Fine hair 3128
Short 2580
Retief 884
Barkhuizen 2157
Hobson 6846
GSAS 2557
Angela 2116
Total 20268
Production and reproduction data
The following production data were recorded on the participating flocks during the reporting year:
• Full pedigrees
• Body weight of ewes before mating
• Reproduction data of all ewes
• Birth weight of kids/lambs
• Body weight of kids/lambs at weaning and subsequent ages
• Fleece weight and fleece sample of ram and ewe kids at second shearing
• Body weight, fleece weight and fleece sample of young sheep ewes and rams at selection age
• Fleece weight and fleece sample of Angora ewes at the winter shearing
• Fleece weight and fleece sample of sheep ewes at shearing.
Genotypes
Information on samples from the GADI-Biobank and Elsenburg Biobank genotyped to date with the Illumina® Ovine
SNP50 BeadChip are summarised in Table 3.
Table 3. Information on samples from the GADI-Biobank and Elsenburg Biobank genotyped to date
Flock Number of
animals Year Genotyped at Funded by
Merino (n=1967)
Elsenburg Hi-Lo Merino flock 91 2011 Geneseek THRIP
Cradock fine wool Merino stud 48 2013 Geneseek Cape Wools
Grootfontein Merino stud 37 2013 Geneseek Cape Wools
Industry sires 15 2015 Geneseek Cape Wools
Industry sires 27 2016 Geneseek Cape Wools
Cradock fine wool Merino stud 5 2016 ARC-BT a ARC
Grootfontein Merino stud 11 2016 ARC-BT ARC
Industry flocks 34 2016 ARC-BT ARC
49
Flock Number of
animals Year Genotyped at Funded by
Elsenburg Hi-Lo Merino flock 408 2018 Geneseek WCAT b
Langgewens Merino flock 24 2018 Geneseek WCAT
Cradock fine wool Merino stud 80 2018 ARC-BT Cape Wools
Grootfontein Merino stud 80 2018 ARC-BT Cape Wools
Cradock fine wool Merino stud 239 2019 Geneseek WCAT
Grootfontein Merino stud 257 2019 Geneseek WCAT
Geoff Kingwill 127 2019 Geneseek WCAT
Eric Naudé 484 2019 Geneseek WCAT
Dohne Merino (n=649)
Industry flocks 39 2015 Geneseek WCAT
Elsenburg 9 2015 Geneseek WCAT
GADI 28 2016 ARC-BT ARC
Dohne ADI 22 2016 ARC-BT ARC
Wauldby Dohne stud 187 2017 ARC-BT ARC
GADI 48 2017 ARC-BT RMRD-SA
Langgewens Dohne Merino flock 25 2018 Geneseek WCAT
Wauldby Dohne stud 223 2019 ARC-BT RMRD-SA
GADI 68 2019 ARC-BT RMRD-SA
SA Mutton Merino (n=75)
Elsenburg 21 2013 Geneseek WCAT
Industry flocks 37 2015 Geneseek WCAT
Industry flocks 17 2016 Geneseek WCAT
Dormer (n=44)
Industry flocks 34 Geneseek WCAT
Elsenburg 10 Geneseek WCAT
Afrino (n=178)
Carnarvon Afrino flock 50 2016 ARC-BT ARC
Carnarvon Afrino flock 128 2018 ARC-BT Cape Wools
Meatmaster (n=89)
Industry flocks 50 2016 ARC-BT ARC
Industry flocks 39 2016 Geneseek WCAT
Dorper (n=88)
Elsenburg 20 2013 Geneseek WCAT
Industry flocks 40 2015 Geneseek WCAT
Industry flocks (White Dorper) 28 2015 Geneseek WCAT
Namaqua Afrikaner (n=53)
Nortier 20 2013 Geneseek WCAT
Industry flocks 33 2016 Geneseek WCAT
Damara
Industry flocks 30 2016 Geneseek WCAT
Pedi
Industry flocks 29 2016 Geneseek WCAT
Black headed Persian
Industry flocks 30 2018 Geneseek WCAT
Fat-tailed sheep
Industry flocks 16 2016 Geneseek WCAT
Total 3248 a ARC-Biotechnology Platform, Onderstepoort b Western Cape Agricultural Trust. Funding for these genotypes was obtained from different funders, including Cape
Wools SA, Red Meat Research and Development SA (RMRD-SA), the Western Cape Agricultural Trust (WCAT), the
National Research Foundation through their Technology and Human Resources for Industry Program (THRIP) and
Research and Technology Fund (RTF) initiatives.
50
PROJECTS AND PUBLICATIONS
The following scientific papers have already been published from projects utilising resources from the GADI-Biobank.
2007 to 2010
Friedrich, H., 2009. Evaluation of microsatellite markers for parentage verification in South African Angora goats.
MSc thesis, University of Pretoria, Pretoria, South Africa.
Goosen, P., Swart, A.C., Storbeck, K. & Swart, P., 2010. Hypocortisolism in the South African goat: The role of
3βHSD. Molecular and Cellular Endocrinology 315, 182-187.
Pieters, A., 2007. Genetic characterization of commercial goat populations in South Africa. MSc thesis, University of
Pretoria, Pretoria, South Africa.
Storbeck, K., Swart, A.C., Slabbert, J.T. & Swart, P., 2007. The identification of two CYP17 alleles in the South
African Angora goat. Drug Metabolism Reviews 39, 467-480.
Storbeck, K., Swart, A.C., Snyman, M.A. & Swart, P., 2008. Two CYP17 genes in the South African Angora goat
(Capra hircus). The identification of three genotypes that differ in copy number and steroidogenic output. The
FEBS Journal 275, 3934-3943.
Storbeck, K., Swart, A.C. & Swart, P., 2009. CYP17 causes hypocortisolism in the South African Angora goat.
Molecular and Cellular Endocrinology 300, 121-125.
Visser, C., Crooijmans, R.P.M.A. & Van Marle-Köster, E., 2010. A genetic linkage map for the South African Angora
goat. Small Ruminant Research 93, 171-179.
Visser, C., Snyman, M.A., Van Marle-Köster, E. & Bovenhuis, H., 2009. Genetic parameters for physical and quality
traits of mohair in South African Angora goats. Small Ruminant Research 87, 27-32.
Visser, C. & Van Marle-Köster, E., 2009. Genetic variation of the reference population for quantitative trait loci
research in South African Angora goats. Animal Genetic Resources Information 45, 113-119.
2011 to 2014
Visser, C., 2011. A molecular approach to genetic improvement of South African Angora goats. PhD thesis, University
of Pretoria, Pretoria, South Africa.
Visser, C., Van Marle-Köster, E., Bovenhuis, H. & Crooijmans, R.P.M.A., 2011. QTL for mohair traits in South
African Angora goats. Small Ruminant Research 100(1), 8-14.
Visser, C., Van Marle-Köster, E. & Friedrich, H., 2011. Parentage verification of South African Angora goats, using
microsatellite markers. South African Journal of Animal Science 41(3), 250-255.
Qwabe, O.S., 2011. Genetic and phenotypic characterisation of the South African Namaqua Afrikaner sheep breed.
MSc thesis, University of Pretoria, Pretoria, South Africa.
Snyman, M.A., Van Marle-Köster, E., Qwabe, S.O. & Visser, C., 2013. Genetic and phenotypic profile of three South
African Namaqua Afrikaner sheep flocks. Grootfontein Agric 13(1), 5-20.
Visser, C., Van Marle-Köster, E., Snyman, M.A., Bovenhuis, H. & Crooijmans, R.P.M.A., 2013. Quantitative trait loci
associated with pre-weaning growth in South African Angora goats. Small Ruminant Research 112(1-3), 15-20.
Garritsen, C., 2014. The impact of DNA parentage verification on EBV estimation and sire ranking in South African
Angora goats. MSc thesis, University of Pretoria, Pretoria, South Africa.
Garritsen, C., Visser, C., Van Marle-Köster, E. & Snyman, M.A., 2014. The impact of DNA parentage verification on
EBV estimation and sire ranking in South African Angora goats. Small Ruminant Research 124, 30-37.
2015
Lashmar, S.F., 2015. SNP variation in SA goat breeds based on the 50k goat bead SNP Chip. MSc thesis, University of
Pretoria, Pretoria, South Africa.
Lashmar, S.F. & Van Marle-Köster, E., 2015. Validation of the 50k Illumina goat SNP chip in the South African
Angora goat. South African Journal of Animal Science 45(1), 56-59.
Sandenbergh, L., 2015. Identification of SNPs associated with robustness and greater reproductive success in the South
African Merino sheep using SNP chip technology. PhD, University of Stellenbosch, Stellenbosch, South Africa.
2016
Dzomba, E.F., Snyman, M.A., Chimonyo, M. & Muchadeyi, F.C., 2016. P4055 Assessing the genomic status of South
African mutton, pelt and dual purpose sheep breeds using genome-wide single nucleotide genotypes. Journal of
Animal Science 94(4), 106.
Lashmar, S.F., Visser, C. & Van Marle-Köster, E., 2016. SNP-based genetic diversity of South African commercial
dairy and fiber goat breeds. Small Ruminant Research 136, 65-71.
Sandenbergh, L., Cloete, S.W.P., Roodt-Wilding, R., Snyman, M.A. & Bester-van der Merwe, A.E., 2016. Evaluation
of the OvineSNP50 chip for use in four South African sheep breeds (Short communication). South African
Journal of Animal Science 46(1), 89-93.
Visser, C., Lashmar, S.F., Van Marle-Köster, E., Poli, M.A. & Allain, D., 2016. Genetic Diversity and Population
Structure in South African, French and Argentinian Angora Goats from Genome-Wide SNP Data. PLoS ONE
11(5): e0154353. doi:10.1371/journal.pone.0154353.
51
2017
Andrews, M., Visser, C. & Van Marle-Köster, E., 2017. Identification of novel variants for KAP 1.1, KAP 8.1 and
KAP 13.3 in South African goats. Small Ruminant Research 149, 176-180.
Andrews, M., 2017. Molecular characterization and polymorphism of three keratin associated protein genes in South
African Angora goats. MSc thesis, University of Pretoria, Pretoria, South Africa.
Snyman, M.A., Storbeck, K-H. & Swart, P., 2017. Evaluation of production and reproduction of three South African
Angora goat CYP17 genotypes. South African Journal of Animal Science 47(4), 478-493.
2018
Dlamini, N.M., 2018. A case-control investigation to evaluate resistance to Haemonchus contortus in South African
Dohne Merino sheep. MSc thesis, University of Pretoria, Pretoria, South Africa.
2019
Dlamini, N.M., Visser, C., Snyman, M.A., Soma, P. & Muchadeyi, F.C., 2019. Genomic evaluation of resistance to
Haemonchus contortus in a South African Dohne Merino flock. Small Ruminant Research 175, 117-125.
Snyman, M.A., Dlamini, N.M., Visser, C., Muchadeyi, F.C. & Soma, P., 2019. Genetic variation in resistance to
Haemonchus contortus in the Wauldby and Grootfontein Dohne Merino flocks. Grootfontein Agric 19(1), 20-
30.
There are already 13 research projects that obtained blood and DNA samples, as well as the relevant phenotypic data
from the bank that have been completed, while there are currently another eight projects underway (Table 4).
Table 4. Projects using samples and data from the blood and DNA bank
Project title Researcher Affiliation
Completed projects
Genetic characterization of commercial goat
populations in South Africa.
Ms A. Pieters University of Pretoria
MSc-study
Developing a genetic marker for the identification
of more hardy Angora goats
Dr K.-H. Storbeck University of Stellenbosch
PhD-study
A molecular approach to genetic improvement of
South African Angora goats (QTL for fibre traits in
South African Angora goats)
Dr C. Visser University of Pretoria
PhD-study
Application of microsatellite markers for parentage
verification in South African Angora goats
Ms H. Friedrich University of Pretoria
MSc-study
Further investigations into the influence of CYP17-
genotypes on reproduction and hardiness in Angora
goats
Dr K.-H. Storbeck
Dr M.A. Snyman
University of Stellenbosch
GADI
Genetic and phenotypic characterisation of
Namaqua Afrikaner sheep
Ms O.S. Qwabe GADI
University of Pretoria
MSc-study
Increasing genetic progress in South African
Angora goats through improved pedigree integrity
Ms C. Garritsen
Dr M.A. Snyman
University of Pretoria
GADI
MSc-study
QTL for body weight in South African Angora
goats
Dr C. Visser
Dr M.A. Snyman
University of Pretoria
GADI
Identification of SNPs associated with robustness
and greater reproductive success in the South
African Merino sheep using SNP chip technology
Dr L. Sandenbergh University of Stellenbosch
PhD-study
Verification of the 50k Illumina Goat SNP chip in
the SA Angora goat population
Mr S.F. Lashmar
Dr C. Visser
University of Pretoria
MSc-study
Molecular characterization and polymorphism of
three keratin associated protein genes in South
African Angora goats
Ms M. Andrews
Dr C. Visser
University of Pretoria
MSc-study
Evaluation of production and reproduction of three
Angora goat CYP17 genotypes
Dr M.A. Snyman
Prof P. Swart
GADI
University of Stellenbosch
A case-control investigation to evaluate resistance
to Haemonchus contortus in South African Dohne
Merino sheep
Dr M.A. Snyman
Dr C. Visser
Dr F.C. Muchadeyi
Mr N.M. Dlamini
GADI
University of Pretoria
ARC
MSc-study
52
Project title Researcher Affiliation
Current projects
Fine mapping of Chromosome 24 and Chromosome
25 for QTL associated with fleece traits in Angora
goats
Dr C. Visser University of Pretoria
Sheep comparative genomics Prof E.F. Dzomba
Dr F.C. Muchadeyi
University of KwaZulu-Natal
ARC
Genome-wide search for signatures of selection
associated with reproduction and body weight in
South African Afrino and Merino sheep
Ms S. Süllwald
Dr C. Visser
Dr M.A. Snyman
Dr W.J. Olivier
University of Pretoria
GADI
MSc-study
Genetic diversity and population structure of
commercial and indigenous SA sheep breeds
Me A. Retief
Dr C. Visser
University of Pretoria
MSc-study
Development of systems for estimating genomic
breeding values in South African wool sheep
Mr N. Nel
Prof S.W.P. Cloete
University of Stellenbosch
Elsenburg Directorate of
Animal Science
PhD-study
Genome-wide search for genetic markers associated
with resistance to Haemonchus contortus in Dohne
Merino sheep
Dr M.A. Snyman
Mr J. Reding
GADI
SA Studbook
Estimation of genomic breeding values for the
South African Merino sheep
Dr R.R. Van der Westhuizen SA Studbook
Analysis of genetic diversity and population
structure of indigenous (fat-tailed) sheep in South
Africa using the OvineSNP50 beadchip
Dr A. Molotsi
Mr I. Malan
University of Stellenbosch
MSc-study
SOURCING OF FUNDING
Applications for funding for the continued maintenance and operation of the Grootfontein Biobank were submitted to
the wool and red meat commodity organisations during January 2019. Unfortunately, these organisations are of the
opinion that it is the responsibility of DAFF to fund the maintenance of the GADI-Biobank. Meetings were
subsequently held with scientists from the University of Pretoria and the Directorate Genetic Resources (DAFF) on the
continued operation and conservation of the resources in the GADI-Biobank. A project proposal was submitted to the
Directorate Genetic Resources requesting funding for the isolation and storage of DNA from the blood samples
currently in the GADI-Biobank.
Subsequent to the abovementioned meeting, a meeting was held with the convenor of the Biodiversity Biobanks South
Africa (BBSA) project in August 2019 at the South African National Biodiversity Institute (SANBI) in Pretoria.
During this meeting it was decided that the objectives of the GADI-Biobank are basically the same as the core biobank
option of the BBSA, and that the GADI-Biobank will participate as a core biobank in BBSA.
A three-year proposal for the Biodiversity Biobanks SA was submitted to the Department of Science & Innovation
(DSI) during October 2019, which was approved in March 2020. A three-year Business Plan and Budget for the
Biodiversity Biobanks SA for 2020/21 to 2022/23 was drafted. A meeting with all role players was held on 29 April
2020 via Zoom, where this Business Plan and Budget proposal was discussed. This proposal was submitted to DSI for
approval.
CONCLUDING REMARKS
The program is running according to schedule and project activities will continue as stipulated in the project protocols.
To date, blood samples from 56 730 Angora goats and sheep have been collected and stored in the blood and DNA
bank. All phenotypic data recorded have been entered into the database. At the moment, no DNA isolations are being
done, as there are no funding or human resources available. The cataloguing of the blood samples in the freezers is also
not progressing as planned, due to the mentioned lack of human resources. Funding for this project is becoming a
problem, but if the participation of the bank in the BBSA becomes a reality, this may alleviate the problem to some
extent.
ACKNOWLEDGEMENTS
All people and institutions that contributed to the project in one way or another are acknowledged for their inputs.
53
Satansbos monitoring and control
J.C.O. du Toit
AIM AND OBJECTIVES
The aim of the Satansbos program is to monitor the distribution and work towards the control of satansbos in South
Africa, with a focus on the eastern Karoo.
The objectives of this program include the following:
• Develop a colony of the biocontrol agent at Grootfontein
• Gather information on the distribution of satansbos, and present this information in an accessible format
• Conduct research into methods for controlling satansbos
• Provide information to interested parties (farmers, public, municipalities, etc.) on the plant and its control
• Collaborate with the “Eradicate Satansbos Action Group” (ESAG).
PROGRAM LAYOUT
The program will incorporate four major facets (Biocontrol, Research, Information, Monitoring), which will be
addressed in individual research projects.
1. Biocontrol. A colony of satansbos beetles will be established at Grootfontein. Once established, this can act as
a source of beetles for interested parties. At Rhodes University there is a beetle producing facility, but drought
in the area has limited production.
2. Research. Research will be conducted at Grootfontein and participating local farms on how the plant is
currently spreading (e.g. in the tributary to the Fish River) and how it can be controlled (e.g. using herbicides).
3. Information. Information on satansbos will be distributed through various media, including Info packs,
articles in newspapers and magazines, and on the GADI website. Informing municipalities of the nature of the
plant and the threat it poses will be a key focus, because many towns have satansbos infestations.
4. Monitoring. The distribution of satansbos will be continuously updated from data collected opportunistically
(e.g. GADI scientists in the field) and actively (e.g. farmer surveys). Spatial information will be made
available to the public and other interested parties.
Grootfontein will collaborate with ESAG, especially in terms of assisting with spatial distribution data, and advice on
herbicide control.
MATERIALS AND METHODS
Biocontrol
The biocontrol production centre at Rhodes University has not yet started making beetles available owing to the
ongoing drought in the region. GADI is on the waiting list for beetles when production has resumed.
Research
No new research projects have been initiated.
Monitoring
Satansbos occurs across nearly the entire latitude of the country, and has been found from 20 to 30 degrees east.
Monitoring is ongoing.
Towns where satansbos has been found are:
Aberdeen, Beaufort West, Bela-Bela, Bethulie, Bloemfontein, Burgersdorp, Carnarvon, Colesberg, Cookhouse,
Cradock, De Aar, De Rust, Despatch, Dewetsdorp, Graaff-Reinet, Hanover, Hutchinson, Jacobsdal, Jagersfontein,
Jansenville, Kendrew, Koffiefontein, Kroonstad, Ladismith, Louis Trichardt, Middelburg (Eastern Cape), Molteno,
Murraysburg, Nieu-Bethesda, Noupoort, Pearston, Polokwane, Postmasburg, Pretoria, Prieska, Queenstown,
Reddersburg, Richmond (Northern Cape), Rosmead, Rouxville, Smithfield, Sterkstroom, Steynsburg, Steytlerville,
Tarkastad, Thohoyandou, Tierpoort, Uniondale, Victoria West, Vosburg, Vuwani, Willowmore, Winburg.
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Towns where satansbos has not been found are:
Alicedale, Aliwal North, Ashton, Barkley West, Barrydale, Bedford, Brandfort, Brandvlei, Britstown,
Buffelsjagsrivier, Calitzdorp, Calvinia, Danielskuil, Dealesville, Fauresmith, Fraserburg, George, Grahamstown,
Griekwastad, Groblershoop, Hankey, Hofmeyr, Hopetown, Humansdorp, Kathu, Kimberley, Kuruman, Laingsburg,
Leeu-Gamka, Loxton, Luckhoff, Marydale, Matjiesfontein, Montagu, Niekerkshoop, Olifantshoek, Oudtshoorn, Parys,
Patensie, Petrusburg, Petrusville, Philipstown, Phillipolis, Prince Albert, Riebeeck East, Ritchie, Sedgefield, Somerset
East, Springfontein, Strydenburg, Suurbraak, Swellendam, Touwsrivier, Trompsburg, Van Der Kloof, Van Wyksdorp,
Wegdraai, Williston.
Final surveys to determine the distribution of satansbos in the Karoo could not be completed owing to the 2020
COVID-19 global pandemic. Attempts to survey these towns will be undertaken, after which results will be published.
PUBLICATIONS
The following have been published since the commencement of the project:
Du Toit, J.C.O., Vorster, H. & Van den Berg, L., 2014. Satansbos (Solanum elaeagnifolium) - the return of the threat in
the Eastern Karoo and Free State. Proceedings of the 2014 Annual Symposium on the Management of Invasive
Alien Plants.
CONCLUDING REMARKS
Satansbos mapping will continue. A biocontrol population will be established when beetles can be sourced.
Unsurveyed towns will be surveyed over the following year.
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Other Pasture Science projects
2019-2020 Report year
Under normal circumstances, botanical surveys in most of the Pasture Science projects are conducted annually from
the end of March until June. As a result of the national lockdown due to the COVID-19 pandemic since the end of
March 2020, these botanical surveys for the projects could only be conducted from July 2020 onwards. The results of
these surveys were therefore not available yet at the time of publication of this report.
The projects are, however, continuing and the results will be reported in the next Research Report. The following
projects were involved:
Fixed season grazing of the mountain paddock in the False Upper Karoo
L. van den Berg
AIM AND OBJECTIVES
The aim of this project is to demonstrate the disadvantages of fixed season grazing on hilly Karoo veld.
The objective of this project is to graze certain paddocks seasonally, year-after-year, to determine the impact on
botanical composition.
PUBLICATIONS
The following have been published from this project during the past ten years:
Van den Berg, L., 2011. Visual landscape changes after 43 years of fixed seasonal grazing in the Eastern Upper Karoo.
Grootfontein Agric 11(1), 19-27.
Mureva, A. & Ward, D., 2016. Spatial patterns of encroaching shrub species under different grazing regimes in a semi-
arid savanna, eastern Karoo, South Africa. African Journal of Range and Forage Science 33, 77-89.
Determining the cattle and sheep grazing impact in the Eastern Mixed Karoo
T.P. Nengwenani and J.C.O. du Toit
AIM AND OBJECTIVES
The aim of this project is to determine the influence that cattle and sheep, grazing the veld simultaneously, have on the
optimal but sustainable use of the veld, while the animals still produce at a high level and the vegetation is still
afforded time to regenerate and improve over time.
The objectives of the project are to:
• Utilise veld with different combinations of sheep and cattle
• Measure the impact on the veld
• Measure the production of the livestock
• Determine the sustainability and profitability of different veld management systems
• Starting 2015, the Boesmanskop trials are used as site for carbon sequestration of rangelands, in collaboration
with EMS-Africa (a follow-on project from ARS-Africa) from Germany.
PUBLICATIONS
The following have been published from this project during the past ten years:
Du Toit, J.C.O., Van den Berg, L. & O’Connor, T.G., 2014. Fire effects on vegetation in a grassy dwarf shrubland at a
site in the eastern Karoo, South Africa. African Journal of Range and Forage Science 32, 13-20.
Du Toit, J.C.O., O’Connor, T.G. & Van den Berg, L., 2015. Photographic evidence of fire-induced shifts from dwarf-
shrub- to grass-dominated vegetation in Nama-Karoo. South African Journal of Botany 101, 148-152.
Du Toit, J.C.O. & Nengwenani, T.P., 2016. Vegetation changes at the Boesmanskop Research Trials, Grootfontein,
2007-2015. Grootfontein Agric 16, 21-32.
Berger, C., Bieri, M., Bradshaw, K., Brümmer, C., Clemen, T., Hickler, T., Kutsch, W.L., Lenfers, U.A., Martens, C.,
Midgley, G.F., Mukwashi, K., Odipo, V., Scheiter, S., Schmullius, C., Baade, J., Du Toit, J.C.O., Scholes, R.J.,
Smit, I.P.J., Stevens, N. & Twine, W., 2019. Linking scales and disciplines: an interdisciplinary cross-scale
approach to supporting climate-relevant ecosystem management. Climatic Change 156, 139-150.
Du Toit, J.C.O., 2019. Drivers of Vegetation Change in the Eastern Karoo. PhD Thesis. University of KwaZulu-Natal,
Durban, South Africa.
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Long-term grazing trials in the Karoo: Camp 6
J.C.O. du Toit
AIM AND OBJECTIVES
The long-term Camp 6 trials are used to demonstrate and quantify vegetation changes over time as influenced by
grazing system and rainfall, and under conditions of steadily increasing atmospheric CO2 concentrations.
The objectives of the observations are to:
• Assist in the capturing and archiving of existing hardcopy proposals, data, reports, maps etc. of historical data
from the Camp 6 and other long-term experiments
• Compile a complete list of plant species present in each experiment and prepare herbarium samples to be
included in the Grootfontein Herbarium
• Measure current plant diversity to determine the effect of 60 years’ worth of grazing treatment on composition
and diversity
• Measure the composition, density and diversity of the woody component in the experiments
• Conduct vegetation surveys using historical methods.
PUBLICATIONS
The following were published from this project during the past decade:
Du Toit, J.C.O., 2011. Why does grass ‘rain’ in the eastern Karoo? Farmers’ Weekly, 9 September 2011. pp 28-29.
Du Toit, J.C.O., Van den Berg, L. & O’Connor, T.G., 2015. Fire in the Nama-Karoo - a shift from dwarf-shrubland to
sparse grassland. 50th Annual Congress of the Grassland Society of Southern Africa p. 49. Pietermaritzburg, South
Africa.
Talore, D.G., Tesfamariam, E.H., Hassen, A., Du Toit, J.C.O., Klampp, K. & Soussana, J.F., 2015. Long-term impacts
of season of grazing on soil carbon sequestration and selected soil properties in the arid Eastern Cape, South Africa.
Plant and Soil 397(1/2), 317-329.
Talore, D.G., Tesfamariam, E.H., Hassen, A., Du Toit, J.C.O., Klampp, K. & Soussana, J.F., 2015. Long-term impacts
of grazing intensity on soil carbon sequestration and selected soil properties in the arid Eastern Cape, South Africa.
Journal of the Science of Food and Agriculture 96(6), https://doi.org/10.1002/jsfa.7302.
Forrestel, E.J., Donoghue, M.J., Edwards, E.J., Jetz, W., Du Toit, J.C. & Smith, M.D., 2017. Different clades and traits
yield similar grassland functional responses. Proceedings of the National Academy of Sciences, 114(4), 705-710.
Hagan, J.G., Du Toit, J.C.O. & Cramer, M.D., 2017. Long-term livestock grazing increases the recruitment success of
epigeal termites: insights from a >75-year grazing experiment in the Karoo, South Africa. African Journal of Range
and Forage Science 34.
Du Toit, J.C.O., Ramaswiela, T., Pauw, M.J. & O’Connor, T.G., 2018. Interactions of grazing and rainfall on
vegetation at Grootfontein in the eastern Karoo. Proceedings of the 2018 Arid Zone Ecology Forum pp. 9-10.
Robertson, South Africa.
Du Toit, J.C.O. & O’Connor, T.G., 2018. Long-term interactions of grazing and rainfall on vegetation composition at
Grootfontein in the eastern Karoo. 53rd Annual Congress of the Grassland Society of Southern Africa p. 35.
Pretoria, South Africa.
Du Toit, J.C.O., Ramaswiela, T., Pauw, M.J. & O’Connor, T.G., 2018. Interactions of grazing and rainfall on
vegetation at Grootfontein in the eastern Karoo. African Journal of Range & Forage Science 35, 267-276.
Du Toit, J.C.O., 2019. Drivers of Vegetation Change in the Eastern Karoo. PhD Thesis. University of KwaZulu-Natal,
Durban, South Africa.
Du Toit, J.C.O. & O’Connor, T.G., 2019. Influence of season of grazing and rainfall over time on vegetation in the
eastern Karoo, South Africa. Proceedings of the 2019 Arid Zone Ecology Forum p. 20. Kimberley, South Africa.
Du Toit, J.C.O. & O’Connor, T.G., 2020. Long-term influence of season of grazing and rainfall on vegetation in the
eastern Karoo, South Africa. African Journal of Range and Forage Science 37, 159-171.
Du Toit, J.C.O & O’Connor T.G. 2020. Investigating the drivers of vegetation change in the eastern Karoo. SAEON
eNews 2020 #04. https://enews.saeon.ac.za/issue-04-2020/investigating-the-drivers-of-vegetation-change-in-the-
eastern-karoo/.
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A monitoring framework towards rangeland monitoring and management within the arid and semi-
arid rangelands of the Eastern and Northern Cape - Middelburg area
J.C.O. du Toit and T.P. Nengwenani
AIM AND OBJECTIVES
The objectives of the Middelburg project and sub-projects are to:
• Conduct herbaceous surveys in four land uses types in the Middelburg area, establishing differences and changes
in vegetation condition and patterns within and between different land use types
• Perform basic resource inventories pertaining to rangeland condition, current grazing capacity, biodiversity
indices and indicator plant species, and compare it with previous inventories where available in order to quantify
changes in temporal scale
• Integrate and interrelate multivariate data to establish patterns within and between land uses and determine the
environmental variables (vegetation type, climate, habitat heterogeneity, land area, historical influence) that are
responsible for the greatest proportion of its variation
• Develop and present Further Education and Farmer Development training products and courses.
A framework towards rangeland monitoring and management within the arid and semi-arid
rangelands of the Eastern and Northern Cape - Carnarvon area
L. van den Berg
AIM AND OBJECTIVES
The aim of this project is to monitor and quantify the effect of feral goats introduced from the Tanqua National Park on
the vegetation at the Carnarvon Research Station.
The objectives of the project are:
• To conduct vegetation surveys at each of the selected monitoring sites over years to describe:
o Plant species composition
o Veld condition
o Grazing capacity
• To make recommendations on future grazing management of the goats at Carnarvon Research Station.
PUBLICATIONS
The following were published from this project:
Van den Berg, L. & Du Toit, J.C.O., 2014. Effects of stocking rate on sheep management and vegetation composition
at Carnarvon. Grootfontein Agric 14(1), 34-41.
Du Toit, J.C.O., Van den Berg, L. & O’Connor, T.G., 2015. A summary of rainfall at the Carnarvon Experiment
Station, 1931-2013. Grootfontein Agric 15(1), 27-35.
Van der Merwe, H., Du Toit, J.C.O., Van den Berg, L. & O’Connor, T.G., 2018. Impact of sheep grazing intensity on
vegetation at the Arid Karoo Stocking Rate Trial after 27 years, Carnarvon, South Africa. Journal of Arid
Environments. 155, 36-45.
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The effects of grazing of different small stock breeds at different stocking rates on Eastern Karoo
vegetation
J.C.O du Toit
AIM AND OBJECTIVES
The aim of this project is to determine interacting effects of various breeds of livestock at different stocking rates on
vegetation composition and structure in the eastern Karoo.
The objectives of the study are to:
• Determine the effects of livestock breeds and stocking rates on vegetation composition and structure
• Determine the patterns of change in the vegetation composition and structure over time
• Determine the role of other environmental variables on vegetation composition and structure
• Provide visual records of changes in vegetation structure and composition using repeat photography
• Provide a site for an Eddy Covariance Flux Tower.
PUBLICATIONS
The following were published from this project:
Simpson, K.J., Ripley, B.S., Du Toit, J.C., Christin, P., Thomas, G.H., Osborne, C.P., 2018. Flammability and post-fire
regrowth are linked in savanna grasses. Chapter 3. In: The influence of fire on grass functional traits. PhD Thesis.
University of Sheffield, England.
Berger, C., Bieri, M., Bradshaw, K., Brümmer, C., Clemen, T., Hickler, T., Kutsch, W.L., Lenfers, U.A., Martens, C.,
Midgley, G.F., Mukwashi, K., Odipo, V., Scheiter, S., Schmullius, C., Baade, J., Du Toit, J.C.O., Scholes, R.J.,
Smit, I.P.J., Stevens, N. & Twine, W., 2019. Linking scales and disciplines: an interdisciplinary cross-scale
approach to supporting climate-relevant ecosystem management. Climatic Change 156, 139-150.
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Other projects in which activities could not take place as planned due to the COVID-19 lockdown are:
A monitoring framework towards rangeland monitoring and management within the arid and semi-
arid rangelands of the Eastern and Northern Cape - Beaufort West area
J.C.O. du Toit
AIM AND OBJECTIVES
The objectives of the Beaufort West project and sub-projects are:
• To establish a repeat-point photograph monitoring programme at the Landmark Foundation with a view of
understanding the utility of this approach for monitoring of landscapes elsewhere
• Monitor the influence of high-density grazing (notably the temporary kraaling aspect) on plant composition,
survival, and potential alien plant invasion
• In collaboration with other partners, conduct vegetation surveys at fixed sites and monitor changes over time.
• To develop and present Further Education and Farmer Development training products and courses.
Fire monitoring in the Karoo and adjacent biomes
J.C.O. du Toit
AIM AND OBJECTIVES
The aim of this project is to monitor vegetation changes following wildfires in the Karoo and adjacent biomes.
The objectives of this project are to:
• Take baseline photographs of areas burnt by wildfires, and boundaries between burnt and unburnt areas
• Undertake baseline compositional surveys of adjacent burnt and unburnt areas
• Monitor change over time of vegetation following burning.
PUBLICATIONS
The following were published from this project:
Du Toit, J.C.O., 2020. Keer so dat die Karoo brand. Landbou Weekblad. 17 September 2020. pp 34-35.
Du Toit, J.C.O., Van den Berg, L., Van Lingen, M., Goodall, V.L. & O’Connor, T.G., 2020. Catastrophic collapses of
sensitive species, including the quiver tree (Aloidendron dichotomum) following fire in the arid Nama-Karoo,
South Africa. 55th Annual Congress of the Grassland Society of Southern Africa pp. 34-35. Virtual Event.
Monitoring changes in vegetation structure using high resolution drone orthophotography
J.C.O. du Toit
AIM AND OBJECTIVES
The aim of the project is to use high resolution drone orthophotographs to map shrub distribution and monitor
vegetation change at Grootfontein Agricultural Development Institute.
The objectives of the project are to:
• Create high resolution orthophotographs of grazing trials and other areas at Grootfontein
• Determine the density and distribution of Karoo dwarf shrubs in areas using orthophotographs
• Examine landscape scale patterns of vegetation cover
• Monitor landscapes over time on Grootfontein and elsewhere
• Use drone imagery to develop a Decision Support System for farmers
• Use drone imagery to develop a model for estimating the density of termite mounds in Karoo rangelands.
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BISMOP (Biome Shift Monitoring Phytometer): Installing a standardised data base for ecological
responses to environmental change
J.C.O. du Toit
AIM AND OBJECTIVES
The aim of this project is to monitor vegetation changes in a common garden experiment, known as BISMOP (Biome
Shift Monitoring Phytometer), in the Karoo and other Southern African biomes.
The objectives of this project are to:
• Create a standardised data base for ecological response to environmental change
• Quantify phenological time series for each species in different biomes.