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    <link>http://hdl.handle.net/10386/74</link>
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        <rdf:li rdf:resource="http://hdl.handle.net/10386/812" />
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    <dc:date>2013-05-14T01:14:03Z</dc:date>
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  <item rdf:about="http://hdl.handle.net/10386/822">
    <title>Helminth ichthyo-parasitic fauna of a South African Sub-Tropical Lake</title>
    <link>http://hdl.handle.net/10386/822</link>
    <description>Title: Helminth ichthyo-parasitic fauna of a South African Sub-Tropical Lake
Authors: Matla, Matsoele Moses
Abstract: The diversity of the helminth parasites of fishes in a clear-water, subtropical Lake&#xD;
Tzaneen, in South Africa was investigated. Of the 527 fish specimens sampled&#xD;
approximately 9000 parasites were collected. There are 38 different parasite species&#xD;
discussed comprising 27 Monogenea, 3 Digenea, 4 Cestoda, 3 Nematoda and 1&#xD;
Acanthocephala. Four new monogenean species are described and these are&#xD;
Dactylogyrus spp. 1 to 4. Three monogenean species are introduced as first records&#xD;
in Africa and these are Actinocleidus fusiformis (Mueller, 1934), Haplocleidus&#xD;
furcatus Mueller, 1937 and Acolpenteron ureteroecetes Fischthal &amp; Allison, 1940.&#xD;
Fourteen monogenean and one acanthocephalan species are discussed as first&#xD;
geographical records for South Africa and these are Gyrodactylus rysavyi Ergens,&#xD;
1973, Dactylogyrus brevicirrus Paperna, 1973, Dactylogyrus cyclocirrus Paperna,&#xD;
1973, Dogielius dublicornis Paperna, 1973, Dogielius sp., Schilbetrema quadricornis&#xD;
Paperna &amp; Thurston, 1968, Quadriacanthus aegypticus El Naggar &amp; Serag, 1986,&#xD;
Quadriacanthus clariadis Paperna, 1961, Scutogyrus gravivaginus (Paperna &amp;&#xD;
Thurston, 1969), Cichlidogyrus quaestio Douëllou, 1993, Cichlidogyrus halli Price &amp;&#xD;
Kirk, 1967, Cichlidogyrus sclerosus Paperna &amp; Thurston, 1969, Cichlidogyrus&#xD;
dossoui Douëllou, 1993, Cichlidogyrus tilapiae Paperna, 1960 and Acanthosentis&#xD;
tilapiae Baylis, 1948. Seven species are discussed as first records for their hosts and&#xD;
these are Cichlidogyrus dossoui, Cichlidogyrus halli and Acanthosentis tilapiae on&#xD;
Oreochromis mossambicus; Dactylogyrus sp. 1 on Barbus radiatus and Barbus&#xD;
trimaculatus; Dactylogyrus sp. 2 on Barbus unitaeniatus; Dactylogyrus sp. 3 and&#xD;
Dactylogyrus sp. 4 on Labeo molybdinus. Gyrodactylus rysavyi is the only species&#xD;
with a first site (gills) record. The other monogenean species discussed are&#xD;
Macrogyrodactylus clarii Gussev, 1961, Macrogyrodactylus karibae (Douellou and&#xD;
Chishawa, 1995), Dactylogyrus afrolongicornis afrolongicornis Paperna, 1973,&#xD;
Dactylogyrus allolongionchus Paperna, 1973, Dactylogyrus spinicirrus (Paperna &amp;&#xD;
Thurston, 1968) and Cichlidogyrus philander (Douëllou, 1993). The digeneans&#xD;
discussed are Glossidium pedatum Looss, 1899 and the larvae of Diplostomum van&#xD;
Nordmann, 1832 and Clinostomum Leidy, 1856. The Cestodes discussed are&#xD;
Proteocephalus glanduligerus (Janicki, 1928) Fuhrmann, 1933, Polyonchobothrium&#xD;
clarias Woodland, 1925 and the larvae of Ligula intestinalis Goeze, 1782 and family Gryporhynchidae. The nematodes discussed are Procamallanus laevionchus (Wedl,&#xD;
1861), Paracamallanus cyathopharynx Baylis, 1923 and larvae of Contracaecum&#xD;
Railliet and Henry, 1912. Monogenea were commonly found on the gills but less on&#xD;
the skin and in the urinary bladder. Digenea were found mainly in the eyes, brain and&#xD;
visceral cavity, with only one species (Glossidium pedatum) present in the intestines&#xD;
of Clarias gariepinus. Cestoda and Nematoda were found in the intestine and body&#xD;
cavity. Only one species of Acanthocephala (Acanthosentis tilapiae) was found in the&#xD;
intestines of Oreochromis mossambicus. No definite seasonal variations of infection&#xD;
and parasite affinities towards the sexes and the sizes of the hosts could be&#xD;
determined. The lake is oligotrophic with the water quality having no influence on the&#xD;
parasite diversity and species richness.
Description: Thesis (Ph.D. (Zoology)) --University of Limpopo, 2012</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10386/812">
    <title>Aspects of the biology of the chestnut-backed sparrow-lark (Eremopterix leucotis) in the Limpopo Province, South Africa</title>
    <link>http://hdl.handle.net/10386/812</link>
    <description>Title: Aspects of the biology of the chestnut-backed sparrow-lark (Eremopterix leucotis) in the Limpopo Province, South Africa
Authors: Dikgale, Mahlodi Lucket
Abstract: Sparrow-larks form a relatively small genus in the family Alaudidae and comprise&#xD;
only seven species distributed widely throughout Africa and parts of the Eurasian&#xD;
landmass. Sparrow-larks are unique amongst larks in that they are sexually&#xD;
dichromatic and exhibit biparental care. The chestnut-backed sparrow-lark&#xD;
Eremopterix leucotis is endemic to Africa with five subspecies recognized based on&#xD;
differences in plumage colouration. The five subspecies are distributed throughout&#xD;
the arid to semi-arid savannas of Africa with two subspecies (E. l. hoeschi and E. l.&#xD;
smithi) occurring in southern Africa. Despite their widespread occurrence and its&#xD;
interest for research on the evolution of characteristics in the family (e.g. being&#xD;
sexually dichromatic and exhibiting biparental care), very little is known of the biology&#xD;
and ecology of the Eremopterix larks. The chestnut-backed sparrow-lark is no&#xD;
exception and most of what we know of the species is based on incidental&#xD;
observations from a few nests. In an attempt to improve our knowledge of this&#xD;
interesting group of species, it was decided to study various aspects of the breeding&#xD;
biology and ecology, moult, vocalizations and geographical variation in the chestnutbacked&#xD;
sparrow-lark.&#xD;
The breeding biology of the chestnut-backed sparrow-lark was studied at Al3 farm&#xD;
(De Loskop) near Mogwadi in the Limpopo Province of South Africa from January&#xD;
2008 to December 2010. Data collected during the study included: breeding&#xD;
seasonality, egg and clutch characteristics, duration of the incubation and nestling&#xD;
periods, nest-site characteristics, the roles and relative contribution of the sexes in&#xD;
the breeding cycle, nestling development, diet and nestling provisioning rate, and&#xD;
breeding success. Chestnut-backed sparrow-larks bred mostly during the dry&#xD;
season, which is from April to September in the study area. Nevertheless, the results&#xD;
revealed that breeding is bimodal with a main peak in breeding activity in late&#xD;
summer and autumn (March to April) and a second smaller peak in spring&#xD;
(September to October). The species showed geographical variation in clutch size&#xD;
with a mean of 1.88 eggs recorded in the study area as opposed to 1.00 recorded in&#xD;
the northern parts of its range. Egg dimensions compared well with measurements&#xD;
obtained from the Nest Record Card Scheme of the Animal Demography Unit,&#xD;
University of Cape Town, South Africa. The mean incubation period of 10.33 days&#xD;
recorded in this study compares favourably with that of other Eremopterix species&#xD;
viii&#xD;
(8–10 days), a genus with some of the shortest incubation periods amongst larks.&#xD;
The mean nestling period of 9.2 days (range: 8–10) in the study area was&#xD;
significantly less than the 10–12 days reported for populations in the northern range&#xD;
of the species, but it compares well with those of other sparrow-larks.&#xD;
Nest site characteristics, which were quantified within a 1 m2 quadrant with the nest&#xD;
as the centre, including nest dimensions, were consistent with those reported in the&#xD;
literature. Chestnut-backed sparrow-larks in the study area preferred to nest in areas&#xD;
with a high percentage of bare ground (median = 67.5%) and very little vegetation&#xD;
cover (median = 25%). Most nests faced in a southerly direction compared to nests&#xD;
in the north of the species’ range, which face in a north-easterly or easterly direction.&#xD;
The species’ preference to face the nests away from the midday sun most probably&#xD;
serves a thermoregulatory function to avoid excessive heat during the warmest parts&#xD;
of the day. Most nests (78.2%) had an apron varying in size from small and&#xD;
insignificant to large and well-developed. The functional significance of the apron&#xD;
remains a matter of conjecture and there was no association between breeding&#xD;
success and presence or absence of the apron. In addition, one pair constructed one&#xD;
nest with and another without an apron, suggesting that individual preference or&#xD;
characteristic is not a determinant factor in the construction of an apron. Both sexes&#xD;
took part in nest construction, incubation and feeding and brooding of nestlings.&#xD;
However, the relative contributions were not entirely symmetrical as males incubated&#xD;
a greater proportion (50.1%) of the time compared to females (43.1%), and the mean&#xD;
and median of male incubation shift lengths were longer than that of females, albeit&#xD;
not statistically significant. However, females made statistically significantly (P &lt;&#xD;
0.05) more nest visits to deliver food compared to males (54.6% vs. 45.5%). The&#xD;
average breeding success, estimated using Mayfield’s method, was 16.1% but there&#xD;
were inter-annual differences with the overall breeding success in 2010 being only&#xD;
8.1% compared to 20.6% of 2008. Known causes of failure included nest&#xD;
depredation, flooding, starvation, nest abandonment and hatching failure.&#xD;
Statistical analysis of morphometric data of live specimens and museum study skins&#xD;
suggest that, in addition to being sexually dichromatic, chestnut-backed sparrowlarks&#xD;
also exhibit mild sexual size dimorphism. However, there was considerable&#xD;
overlap in these measurements between the sexes and as a result the biological&#xD;
significance of this sexual size dimorphism may be negligible. Nevertheless, the&#xD;
ix&#xD;
results show chestnut-backed sparrow-lark males tend to have longer wings and tails&#xD;
compared to females. This may be adaptive with respect to the extended display&#xD;
flights that males perform during the breeding season. Interestingly, the mean mass&#xD;
of breeding females in the study area was significantly more compared to males,&#xD;
whereas the SAFRING database, representing data recorded throughout the year,&#xD;
showed no significant differences in the mean mass between the sexes. The greater&#xD;
mass of breeding females may relate to physiological changes associated with the&#xD;
acquisition of resources and the development of structures and tissues associated&#xD;
with egg-laying and egg-production.&#xD;
Larks rely heavily on vocalizations to attract mates and advertise territories. Not&#xD;
surprisingly, the study revealed a rich vocal repertoire for the chestnut-backed&#xD;
sparrow-lark. The analysis of the vocalizations shows that chestnut-backed sparrowlarks&#xD;
have a display song performed by males, a sub-song sung by both sexes and&#xD;
various different calls used in different contexts, e.g. flight and alarm calls. The study&#xD;
also presents the first analysis and description of the vocalizations of nestlings. An&#xD;
interesting feature of the vocalizations of the chestnut-backed sparrow-larks was that&#xD;
they performed hetero-specific vocal mimicry, which was incorporated in the subsong.&#xD;
Moult is a relatively unknown aspect in the annual cycle of the majority of larks.&#xD;
Chestnut-backed sparrow-larks undergo post-breeding moult, which is an adaptation&#xD;
to reduce the conflict between moult and breeding as both activities have high&#xD;
energy demands. The moult study also showed that they undergo a partial moult in&#xD;
mid-winter, involving the inner-most secondaries and some of the contour feathers.&#xD;
The results of this study shed valuable light on the natural history of this species and&#xD;
contributed significantly to ornithology and our growing understanding of the biology&#xD;
and ecology of the family. The results can also form a basis for future inter- and&#xD;
intraspecific comparative studies. The study illustrates the importance of undertaking&#xD;
long term studies of species to account for inter-annual differences in various&#xD;
ecological parameters.
Description: Thesis (M.Sc. (Zoology)) -- University of Limpopo, 2012</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10386/807">
    <title>Breeding habitat of Blue Crane (Anthropoides Paradiseus) in Mpumalanga Province, South Africa</title>
    <link>http://hdl.handle.net/10386/807</link>
    <description>Title: Breeding habitat of Blue Crane (Anthropoides Paradiseus) in Mpumalanga Province, South Africa
Authors: Mmonoa, Ernest Mmaphuti
Abstract: The aim of this study was to determine the breeding habitat of Blue Crane (Anthropoides&#xD;
paradiseus) by investigating the home range, habitat selection and habitat suitability.&#xD;
Geographic Information System (GIS) was used as the main tool for analysis.&#xD;
Home range sizes of Blue Cranes were studied during the breeding season using direct&#xD;
observation method. A 50% and 95% Adaptive Kernel was used to estimate home range sizes. The&#xD;
home range sizes were 9.0 ha and 43.5 ha for 50% and 95% Adaptive Kernel, respectively. All the&#xD;
nests were located within 50% Adaptive Kernel, often referred to as core area. The nests were&#xD;
located in agricultural land (mainly pasture) and close to water sources.&#xD;
Habitat selection was studied at nest sites (n = 74) and random sites (n = 200) following site&#xD;
attribute design. The Blue Crane showed a preference to breed in agricultural lands, close&#xD;
proximity to water sources, higher elevation areas, within north eastern sandy highveld&#xD;
vegetation, and north facing slope. The Blue Crane also avoided anthropogenic factors such as&#xD;
built-up land, roads and railway line.&#xD;
ModelBuilder extension of ArcGIS software was used to construct a breeding habitat suitability&#xD;
model for Blue Cranes. Nine habitat variables (water source, slope, aspect, elevation, land use,&#xD;
vegetation, built-up land, roads and railway line) were used in the model. The model was&#xD;
constructed using reclassify and weighted overlay command. Highly suitable sites accounted for&#xD;
601, 448 ha, while moderately suitable sites accounted for 823, 593 ha, and least suitable sites&#xD;
accounted for 3, 000, 153 ha.&#xD;
This study demonstrated the effective use of GIS technology in analysing the breeding ecology of&#xD;
Blue Crane. The GIS technology provided capabilities for capturing and analysing varied and&#xD;
large data. It was also evident that availability of accurate and complete species data remains&#xD;
vital to enable the full utilization of the GIS technology.
Description: Thesis (M.Sc. (Zoology)) --University of Limpopo, 2009</description>
    <dc:date>2009-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10386/720">
    <title>An individual-based approach to genetic management in the game industry, with specific reference to parentage determination in free-ranging populations</title>
    <link>http://hdl.handle.net/10386/720</link>
    <description>Title: An individual-based approach to genetic management in the game industry, with specific reference to parentage determination in free-ranging populations
Authors: Ehlers, Karen
Description: Thesis (Ph.D. (Zoology)) -- University of Limpopo, 2012</description>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </item>
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