La pollution particulaire de l'air provient de différentes sources dont le trafic routier et est reconnue pour avoir un impact significatif sur la santé. Grâce à un meilleur contrôle des émissions à l'échappement, la contribution des émissions non liées à l’échappement à la pollution de l’air s’accroit. Dans celles-ci- se trouvent les particules d'usure des freins dont la toxicité est mal caractérisée. Dans cette thèse nous avons travaillé sur des particules d’usure de freins recueillies sur différents véhicules avec pour objectif une caractérisation physico-chimique et toxicologique de ces particules et de leur fraction nanométrique. Ces particules présentent une hétérogénéité de forme et de taille avec une fraction nanoparticulaire dont le fer et le cuivre sont les composants principaux. L’étude toxicologique a été réalisée sur un modèle 3D de cellules épithéliales bronchiques humaines (Calu-3) cultivées en Transwell® permettant d’obtenir une barrière épithéliale respiratoire. Les nanoparticules (NPs) jusqu’à 100 µg/cm² n’affectent pas la viabilité cellulaire à 24h et n’induisent pas de réponse-proinflammatoire. La technique de « single Particle ICP-MS » nous a permis de démontrer qu’elles sont capables de traverser la barrière respiratoire en faible quantité, probablement par transcytose. De plus ces NPs induisent l’expression et la production de la mucine MUC5AC par un mécanisme dépendant de la voie du récepteur à l'EGF. Dans un test de blessure réalisé sur un épithélium pré-exposé aux NPs, la vitesse de réparation de la lésion n’est pas modifiée mais la prolifération est plus importante que dans un épithélium non pré-exposé. En conclusion, la fraction nanoparticulaire métallique présente dans les particules d'usure des freins traverse faiblement la barrière épithéliale bronchique, induit la production de mucus et active la prolifération lors de la réparation ce qui pourrait suggérer une implication dans le remodelage des voies respiratoires. / Particulate air pollution results from a variety of sources including road traffic and is known to have a significant impact on health. With improved exhaust emissions control, the contribution of non-exhaust emissions to air pollution is increasing. In these are brake wear particles whose toxicity is poorly characterized. In this thesis we worked on brake wear particles collected on different vehicles with the aim of achieving a physico-chemical and toxicological characterization of these particles and their nanometric fraction. These particles have a heterogeneity of shape and size with a nanoparticulate fraction of which iron and copper are the main components. The toxicological study was performed on a 3D model of human bronchial epithelial cells (Calu-3) grown in Transwell® to obtain a pertinent respiratory epithelial barrier. Nanoparticles (NPs) do not affect cell viability up to 100 μg/cm² at 24 hours and do not induce a proinflammatory response. The technique of "Single Particle ICP-MS" has allowed us to demonstrate that particles are able to cross the respiratory barrier in small quantities, probably by transcytosis. In addition, these NPs induce expression and production of MUC5AC mucin by a mechanism dependent on the EGFR pathway. In a wound healing test carried out on an epithelium pre-exposed to the NPs, kinetic repair of the lesion is not modified but the proliferation is greater than in a non-pre-exposed epithelium. In conclusion, the metal nanoparticulate fraction present in brake wear particles weakly crosses the bronchial epithelial barrier, induces production of mucus and activates the proliferation during the repair which could suggest an implication in the remodeling of the airways.

Les particules issues de la pollution sont responsables de millions de morts prématurées. Les nanoparticules (au diamètre inférieur à 100 nm) atteignent les alvéoles où elles rencontrent la barrière alvéolo-capillaire. Cette barrière est composée d'un épithélium alvéolaire et d'un endothélium, dos à dos contre une membrane ultrafine (environ 0.2 µM), soumis à une stimulation constante exercée par l'inflation cyclique des alvéoles et par le cisaillement dû à la circulation sanguine. Nous nous sommes appliqués à développer un modèle in vitro innovant de cette barrière alvéolo-capillaire afin d'observer les interactions des nanoparticules avec cette barrière. Dans un premier temps, nous avons développé un substrat micro-fabriqué qui reproduit les propriétés géométriques et physiques de la membrane alvéolo-capillaire. Sur cette membrane, nous avons mis en place une co-culture de cellules épithéliales alvéolaires (A549) et endothéliales (HUVEC). Grâce à une étude de microscopie confocale, nous avons observé le comportement de ce modèle en termes d'étanchéité et de fonctions biologiques. Finalement nous avons observé les interactions entre des nanoparticules de silice et notre modèle en termes de toxicité, d'internalisation et de translocation. Dans une seconde partie, nous avons développé une puce microfluidique à deux chambres qui permet de reproduire autour de notre modèle de co-culture le microenvironnement spécifique des alvéoles pulmonaires. Des études de conception mécanique et l'optimisation de méthodes de microfabrication nous ont permis de générer une puce réversible compatible avec de la culture à long-terme et de l'observation en live par microscopie confocale. Dans une troisième partie, nous avons commencé un travail préliminaire visant à intégrer des cellules pluripotentes induites différenciées dans notre modèle in vitro. Nous avons travaillé à optimiser deux protocoles de différentiation sur une lignée commerciale: vers un endothélium et vers un épithélium alvéolaire. Finalement, nous proposons ici un modèle in vitro offrant de nombreux avantages: une importante communication intercellulaire via leur co-culture sur une membrane ultrafine, une culture long-terme observable au quotidien, la reproduction des stimuli dynamiques de l'environnement alvéolo-capillaire in vivo et la possibilité d'effectuer des tests d'interaction et de translocation de nanoparticules. / Pollutions particles are responsible for millions of premature death. Nanoparticles (with a diameter below 100 nm) reach the alveolar sacs where they encounter the alveolar capillary barrier. This barrier is constituted of an alveolar epithelium and an endothelium back to back on an ultra-thin membrane (about 0.2 µm), submitted to constant stimuli due to cyclic alveolar inflation and blood flow shear stress. We focused here on developing an innovative in vitro model of the alveolar capillary barrier to study the interactions of the nanoparticles with this barrier. Firstly, we have developed a micro-engineered substrate reproducing the geometrical and physical properties of the alveolar capillary membrane. We implemented the co-culture of an alveolar epithelium (A549) and an endothelium (HUVEC) on this membrane. We used confocal microscopy to observe the behavior of our model regarding barrier integrity and specific phenotypes. Finally, we observed the interactions between Silica nanoparticles and our model in terms of toxicity, internalization and translocation. Secondly, we developed a two-chamber microfluidic chip reproducing the specific microenvironment of the alveoli around our co-culture model. Studies of mechanical design and fabrication processes optimization allowed for the generation of a reversible chip compatible with long-term culture and live observation with a confocal microscope. Thirdly, we launched preliminary experiments aiming at the integration of differentiated induced pluripotent stem cells in our in vitro model. We worked on optimizing two directed differentiation protocols: towards an endothelium and towards an alveolar epithelium.Finally, we present here an in vitro model with numerous features: a close-contact co-culture on an ultra-thin membrane enabling important intercellular communication, a long-term culture allowing for live monitoring, mimicking the in vivo dynamic stimuli of the alveolar capillary barrier microenvironment and the possibility for nanoparticles interaction and translocation studies.

Les hélicases sont des protéines qui utilisent l'énergie fournie par l'hydrolyse de l'ATP ou du GTP pour catalyser la disjonction des doubles hélices d'ADN ou d'ARN. Cette activité de déroulement de double brin leur confère un rôle essentiel dans le métabolisme des acides nucléiques, le maintien de la stabilité du génome et les processus de signalisation cellulaire. En conséquence, ils sont impliqués dans des processus aussi divers que le vieillissement, l'apparition de cancers, l'immunité innée. Cette thèse est axée sur la compréhension de la fonction et des mécanismes moléculaires de deux hélicases différentes et le manuscrit est donc divisé en deux parties. Le premier est dédié à l'hélicase RIG-I, une hélicase à ARN, exprimée lorsque les cellules leucémiques cessent de proliférer et sont induites à se différencier en granulocytes, indispensables à la reconnaissance de l'ARN double brin des virus, initiant la protection des cellules contre la réplication des génomes viraux. Le mécanisme d'action de RIG-I est bien décrit dans le contexte d'une infection virale. Mais dans le cas de la différenciation des cellules myéloïdes, l'intervention de RIG-I et son rôle dans la balance la prolifération / différenciation restent incomplets. En effet, les interactions RIG-I en particulier avec les ligands cellulaires ne sont pas totalement comprises. La première partie de mon travail consistait à tenter d'isoler et de caractériser les partenaires de RIG-I lors de la différenciation des cellules leucémiques NB4. La seconde est consacrée à l'étude des mécanismes sous-jacents aux G-quadruplexes résolus par les hélicases. Plusieurs questions subsistent quant aux interactions entre la structure particulière des G-quadruplexes et ces enzymes. Une hélicase de Bacteroides sp 3_1_23, BsPif1, a été choisie pour comparer et caractériser l'interaction entre les G-quadruplexes et l'ADN canonique de Watson-Crick. Dans les deux parties du travail, les interactions ont été étudiées par des techniques biochimiques utilisant soit une lignée cellulaire ou une protéine purifiée et des acides nucléiques synthétiques. / Helicases are proteins that utilize the energy provided by the hydrolysis of ATP or GTP to catalyse the disjunction of double DNA or RNA helices. This double strand unwinding activity gives them an essential role in the metabolism of nucleic acids, the maintenance of the genome stability and cell signalling processes. As a result, they are involved in processes as diverse as aging, the appearance of cancers, innate immunity. This thesis is focused on the understanding of the function and the molecular mechanisms of two different helicases and the manuscript is therefore divided in two parts. The first one is dedicated to the RIG-I helicase, an RNA helicase, expressed when leukemic cells stop proliferate and are induced to differentiate in granulocytes, which are essential in the recognition of double-stranded RNA of viruses, initiating the protection of the cells against the replication of the viral genomes. The mechanism of action of RIG-I is well described in the context of viral infection. But in the case of the differentiation of myeloid cells, the intervention of RIG-I and its influence on the equilibrium proliferation / differentiation remains incomplete. Indeed, RIG-I interactions in particular with cellular ligands are not fully understood. The first part of my work consisted in an attempt to isolate and characterize RIG-I partners during differentiation of NB4 leukemic cells. The second one is devoted to the study of mechanisms underlying G-quadruplexes resolving by helicases. Several questions remain about the interactions between the particular structure of G-quadruplexes and these enzymes. A Bacteroides sp 3_1_23 helicase, BsPif1, was chosen to compare and characterize the interaction between G-quadruplexes and canonical Watson-Crick DNA. In the two parts of the work, the interactions were investigated by biochemical techniques using either a cell line or purified protein and synthetic nucleic acids.

We investigated four different problems using coarse grained computational models : self-assembly of single stranded (ss) DNA virus, ejection dynamics of double stranded(ds) DNA from phages, translocation of ssDNA through MspA protein pore, and segmental dynamics of a polymer translocating through a synthetic nanopore. In the first part of the project, we investigated the self-assembly of a virus with and without its genome. A coarse-grained model was proposed for the viral subunit proteins and its genome (ssDNA). Langevin dynamics simulation, and replica exchange method were used to determine the kinetics and energetics of the self-assembly process, respectively. The self-assembly follows a nucleation-growth kind of mechanism. The ssDNA plays a crucial role in the self-assembly by acting as a template and enhancing the local concentration of the subunits. The presence of the genome does not changes the mechanism of the self-assembly but it reduces the nucleation time and enhances the growth rate by almost an order of magnitude. The second part of the project involves the investigation of the dynamics of the ejection of dsDNA from phages. A coarse-grained model was used for the phage and dsDNA. Langevin dynamics simulation was used to investigate the kinetics of the ejection. The ejection is a stochastic process and a slow intermediate rate kinetics was observed for most ejection trajectories. We discovered that the jamming of the DNA at the pore mouth at high packing fraction and for a disordered system is the reason for the intermediate slow kinetics. The third part of the project involves translocation of ssDNA through MspA protein pore. MspA protein pore has the potential for genome sequencing because of its ability to clearly distinguish the four different nucleotides based on their blockade current, but it is a challenge to use this pore for any practical application because of the very fast traslocation time. We resolved the state of DNA translocation reported in the recent experimental work . We also investigated two methods for slowing down the translocation process: pore mutation and use of alternating voltage. Langevin dynamics simulation and Poisson Nernst Planck solver were used for the investigation. We demonstrated that mutation of the protein pore or applying alternating voltage is not a perfect solution for increasing translocation time deterministically. Both strategies resulted in enhanced average translocation time as well as the width of the translocation time distribution. The increase in the width of the translocation time distribution is undesired. In the last part of the project, we investigated the applicability of the polyelectrolyte theory in the computer simulation of polyelectrolyte translocation through nanopores. We determined that the Debye Huckel approximation is acceptable for most translocation simulations as long as the coarse grained polymer bead size is comparable or larger than the Debye length. We also determined that the equilibrium translocation theory is applicable to the polyelectrolyte translocation through a nanopore under biasing condition. The unbiased translocation behavior of a polyelectrolyte chain is qualitatively different from the Rouse model predictions, except for the case where the polyelectrolyte is very small compared to the nanopore. .

Typescript (photocopy). / Digitized by Kansas Correctional Industries

Call number: LD2668 .T4 1985 S757 / Master of Science

Translocation involves the movement of organisms, by human intervention, from one area to other suitable (receptor) habitats. In a conservation context, translocation can be employed to support species preservation, population restoration and/or for ecological research. Despite decades of internationally published research, translocation remains a controversial endeavour. However, due to continual degradation and fragmentation of natural habitats in the face of human development, translocation is becoming a vital component of conservation efforts. Prior to the development of an Exxaro coal mine in Mpumalanga, a population of an endangered Highveld succulent species, Frithia humilis Burgoyne (Aizoaceae/Mesembryanthemaceae), was saved from extirpation by means of translocation. Three receptor habitats were identified within the distribution range of the species. The largest part of the donor population was transplanted to sandstone outcrops of the Ecca Group (Karoo Supergroup), resulting in four subpopulations residing on geological substrates typical of the species’ habitat. The remaining portion of the donor population was experimentally translocated to two habitats containing non-native geologies, namely sedimentary outcrops of the Wilge River Formation (Waterberg Group) and (igneous) felsite oucrops of the Rooiberg Group (Transvaal Supergroup). A control population was identified, occupying Ecca and Dwyka Group (Karoo Supergroup) sediments, as a measure to compare the response of translocated populations. A monitoring programme, utilising a plant age classification system, was initiated in February of 2010 to elucidate demographic trends and to gauge the response of translocated populations to novel environments. Plant survival, plant growth, flowering, fruiting (representing reproductive response) and seedling emergence were chosen as indicators to measure translocation success over the short term. Furthermore, quantitative and qualitative entomological investigations into the identity of possible F. humilis pollinators, as well as the presence of pollinator species at receptor habitats, were made. A repeatable methodology for post-translocation monitoring and scientifically sound baseline data for future comparative purposes were successfully established. Initial results showed that F. humilis subpopulations replanted on Ecca standstones had positive responses to translocation: Subpopulations survived and all but one increased in size. Individual plant growth increased, higher reproductive output was evident and seedling emergence was pervasive. Positive responses indicated that F. humilis populations translocated onto typical geologies had the potential to establish and persist over three years. Knowledge of this early success is of immense value to the conservation of the species, as a limited number of known natural populations remain. Coal mining, targeting coal seams underlying typical F. humilis habitats, is also likely to remain a threat. The viability of translocating F. humilis populations to non-typical geological substrates has shown limited efficacy. Poor survival along with inferior reproductive response confirmed Wilge River Formation outcrops as poor receptor sites for translocated F. humilis populations. Rooiberg felsite outcrops also proved to be dubious receptor sites, primarily since there was a downward trend in seedling emergence over time, suggesting inferior germination conditions. Nevertheless, translocation to non-native geological substrates did not have disastrous short-term consequences for these populations, since flowering, fruit production and seedling emergence continued, albeit at reduced (or continually declining) rates. Potential pollinator species of F. humilis were not revealed through quantitative surveys of insect diversity. Qualitative surveys proved more efficient and accurate at pinpointing insect pollinator species. This study provided the first evidence of Apidae, Megachilidae (Hymenoptera) and Bombyliidae (Diptera) insect species pollinating F. humilis. The generalist nature of the plant-pollinator relationship, as well as the presence of generalist pollinator species at some receptor habitats, probably contributed to the initial positive response of F. humilis flowering and fruiting after translocation. Results from this study, however promising, should be viewed as initial indications of translocation success. The literature review revealed a plethora of literature recommending post-translocation monitoring programmes for five years to several decades. This study confirmed that successful establishment of F. humilis can be determined after three years, but that long-term monitoring is required to evaluate persistence. / MSc (Environmental Sciences), North-West University, Potchefstroom Campus, 2015

Translocation involves the movement of organisms, by human intervention, from one area to other suitable (receptor) habitats. In a conservation context, translocation can be employed to support species preservation, population restoration and/or for ecological research. Despite decades of internationally published research, translocation remains a controversial endeavour. However, due to continual degradation and fragmentation of natural habitats in the face of human development, translocation is becoming a vital component of conservation efforts. Prior to the development of an Exxaro coal mine in Mpumalanga, a population of an endangered Highveld succulent species, Frithia humilis Burgoyne (Aizoaceae/Mesembryanthemaceae), was saved from extirpation by means of translocation. Three receptor habitats were identified within the distribution range of the species. The largest part of the donor population was transplanted to sandstone outcrops of the Ecca Group (Karoo Supergroup), resulting in four subpopulations residing on geological substrates typical of the species’ habitat. The remaining portion of the donor population was experimentally translocated to two habitats containing non-native geologies, namely sedimentary outcrops of the Wilge River Formation (Waterberg Group) and (igneous) felsite oucrops of the Rooiberg Group (Transvaal Supergroup). A control population was identified, occupying Ecca and Dwyka Group (Karoo Supergroup) sediments, as a measure to compare the response of translocated populations. A monitoring programme, utilising a plant age classification system, was initiated in February of 2010 to elucidate demographic trends and to gauge the response of translocated populations to novel environments. Plant survival, plant growth, flowering, fruiting (representing reproductive response) and seedling emergence were chosen as indicators to measure translocation success over the short term. Furthermore, quantitative and qualitative entomological investigations into the identity of possible F. humilis pollinators, as well as the presence of pollinator species at receptor habitats, were made. A repeatable methodology for post-translocation monitoring and scientifically sound baseline data for future comparative purposes were successfully established. Initial results showed that F. humilis subpopulations replanted on Ecca standstones had positive responses to translocation: Subpopulations survived and all but one increased in size. Individual plant growth increased, higher reproductive output was evident and seedling emergence was pervasive. Positive responses indicated that F. humilis populations translocated onto typical geologies had the potential to establish and persist over three years. Knowledge of this early success is of immense value to the conservation of the species, as a limited number of known natural populations remain. Coal mining, targeting coal seams underlying typical F. humilis habitats, is also likely to remain a threat. The viability of translocating F. humilis populations to non-typical geological substrates has shown limited efficacy. Poor survival along with inferior reproductive response confirmed Wilge River Formation outcrops as poor receptor sites for translocated F. humilis populations. Rooiberg felsite outcrops also proved to be dubious receptor sites, primarily since there was a downward trend in seedling emergence over time, suggesting inferior germination conditions. Nevertheless, translocation to non-native geological substrates did not have disastrous short-term consequences for these populations, since flowering, fruit production and seedling emergence continued, albeit at reduced (or continually declining) rates. Potential pollinator species of F. humilis were not revealed through quantitative surveys of insect diversity. Qualitative surveys proved more efficient and accurate at pinpointing insect pollinator species. This study provided the first evidence of Apidae, Megachilidae (Hymenoptera) and Bombyliidae (Diptera) insect species pollinating F. humilis. The generalist nature of the plant-pollinator relationship, as well as the presence of generalist pollinator species at some receptor habitats, probably contributed to the initial positive response of F. humilis flowering and fruiting after translocation. Results from this study, however promising, should be viewed as initial indications of translocation success. The literature review revealed a plethora of literature recommending post-translocation monitoring programmes for five years to several decades. This study confirmed that successful establishment of F. humilis can be determined after three years, but that long-term monitoring is required to evaluate persistence. / MSc (Environmental Sciences), North-West University, Potchefstroom Campus, 2015

Thesis (PhD (Botany and Zoology))--Stellenbosch University, 2008. / ENGLISH ABSTRACT: The worldwide movement of biota is of substantial concern for the conservation of biodiversity. The movement of species takes place at three different scales. These are translocations of indigenous species within their natural distribution ranges, the translocation of species outside their natural distribution ranges within geopolitical boundaries (i.e. extralimital introductions) and the translocation of species outside geopolitical boundaries and their natural distribution ranges (i.e. extraregional introductions). Ungulates are extensively translocated at each of these scales and each scale of translocation is expected to have different impacts on biodiversity. Ungulates are translocated for conservation purposes such as reintroducing species to places where they have previously gone extinct and to mitigate inbreeding in small, isolated populations. Ungulates are also extensively translocated for economic and recreational reasons, such as for sport hunting. Translocations for sport hunting include indigenous, extralimital and extraregional species. Concerns for translocations of indigenous species are largely for the loss of genetic diversity through the mixing of genetically distinct populations, and concerns for extralimital and extraregional translocations are for impacts on indigenous biodiversity such as through herbivory, competition, hybridization and disease transmission. This thesis investigates the extent of ungulate introductions globally and at a finer resolution in South Africa. It investigates the pathways, drivers and impacts of ungulate introductions and it also investigates the use of surrogates for genetic distinctiveness for advising the translocation of indigenous ungulates. The study finds that ungulate translocations have been extensive and have lead to the homogenization of ungulate assemblages in countries globally and at a quarter-degree grid-cell resolution in South Africa. Zoos were identified as a potential introduction pathway for extraregional ungulates globally and in South Africa extraregional introductions have made ungulate assemblages more different; whereas large numbers of extralimital introductions have made ungulate assemblages more similar. The homogenization of ungulate species in South Africa has increased with time, due to increased numbers of translocations, particularly of extralimital species. In South Africa translocations have most recently been made to high-income areas with high human population density and high livestock density; whereas in the 1960s ungulates were introduced to areas species poor for indigenous ungulates and marginal for livestock. In South Africa, long distance translocations of indigenous species extralimitally has resulted in extensive range expansions of a magnitude greater than predicted range changes as a result of predicted climate change. When the use of surrogates of genetic distinctiveness for advising translocations was investigated for Africa, the East African rift valley was found to be important in delineating genetic distinctiveness and translocations across this feature should be prevented. Major rivers in Africa also showed potential for delineating genetic distinctiveness in ungulates, but relevant phylogeographic data are needed to confirm this. Sufficient evidence for the impacts of non-indigenous ungulates on biodiversity both in South Africa and globally is lacking despite substantial concern for their impacts. It is suggested that to demonstrate the impacts of non-indigenous ungulates exclosure and enclosure experiments should be used and population declines in indigenous species should be shown. / AFRIKAANSE OPSOMMING: Verskuiwing van plante en diere wêreldwyd lei tot groot kommer in gevolge die bewaring van biodiversiteit. Verskuiwings vind op drie skale plaas, naamlik, die verskuiwing van inheemse spesies binne hulle natuurlike verspreidingsgebied, die verskuiwing van spesies buite hul natuurlike verspreidingsgebied maar binne landsgrense (d.w.s. buite limiet verskuiwings), en die verskuiwing van spesies buite hul natuurlike verspreidingsgebied en buite landsgrense (d.w.s. buite grondgebied verskuiwings). Grootskaalse verskuiwing van hoefdiere vind op al drie skale plaas. Verskuiwing op elk van die skale sal na verwagting biodiversiteit verskillend beïnvloed. Hoefdiere word ook vir bewaringsdoeleindes verskuif, bv. die herbevolking van ‘n gebied waar die spesies uitgesterf het, asook om genetiese probleme wat gepaardgaan met klein bevolkingsgroottes te vermy. Hoefdiere word ook verskuif vir ekonomiese- en ontspannings redes, o.a. vir sportjag, en sluit verskuiwings op al drie skale in. Kommer oor verskuiwings binne ‘n spesies se verspreidingsgebied rus hoofsaaklik op die verlies van genetiese diversiteit a.g.v. die vermenging van vorig genetiese eiensoortige bevolkings, terwyl op die ander twee skale kommer hoofsaaklik gebaseer is op die impakte van kompetisie, interteling, predasie, herbivoor effek, en die verspreiding van parasiete op inheemse biodiversiteit. Hierdie proefskrif ondersoek die omvang van hoefdier verskuiwings globaal asook in Suid Afrika. Die verskuiwingsweë, oorsake en impakte van verskuiwings word hier ondersoek, asook die maatstawwe van genetiese eiensoortigheid om advies oor verskuiwings te verskaf. Die bevindings toon op ekstensiewe verskuiwing van hoefdiere wat eenvormigheid van hoefdier spesiesamestellings wêreldwyd bevorder het, sowel as op ‘n kwartgraad skaal in Suid Afrika. Dieretuine is geïdentifiseer as ‘n potensiële bron van buite grondgebied verskuiwings. In Suid Afrika het buite grondgebied verskuiwings hoefdier spesiesamestellings minder eenvormig gemaak, terwyl buite limiet verskuiwings hoefdier samestellings binne Suid Afrika meer eenvormig gemaak het. Eenvormigheid in hoefdier spesiesamestellings het met tyd in Suid Afrika toegeneem as gevolg van ‘n toename in veral buite limiet verskuiwings. In Suid Afrika is verskuiwings mees onlangs na hoë-inkomste gebiede met hoë menslike bevolkingsen veëdigthede gemaak. In die sestiger jare is hoefdiere egter verskuif na gebiede waar min inheemse hoefdiere voorgekom het en wat marginaal was vir veëboerdery. In Suid Afrika het langafstand buite limiet verskuiwings versoorsaak dat die verspreidingsgebiede van sekere hoefdier spesies groter is as wat die geval sal wees met voorspelde klimaatsveranderinge. Waneer surogaat inligting gebruik word om genetiese verskille tussen bevolkings te identifiseer om verskuiwings te adviseer, word die Oos Afrika Rift vallei geïdentifiseer as ‘n belangrike breuk tussen bevolkings. Verskuiwings oor die vallei moet verkieslik nie plaasvind nie. Groot riviere in Afrika speel ‘n soortgelyke rol, maar verdere genetiese inligting is nodig om dit te bevestig. Alhoewel kommer oor die impak van verskuiwings groot en teoreties verdedigbaar is, bestaan daar te min konkrete bewyse vir die impakte in Suid Afrika. Daar word voorgestel dat manipuleringseksperimente uitgevoer moet word om impakte te demonstreer, en dat aandag veral gegee moet word aan die demonstrasie van impakte op inheemse spesies.

published_or_final_version / abstract / Pathology / Doctoral / Doctor of Philosophy