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Auswahl der wissenschaftlichen Literatur zum Thema „Cassava – Diseases and pests – South Africa“
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Zeitschriftenartikel zum Thema "Cassava – Diseases and pests – South Africa"
Okonya, Joshua, Walter Ocimati, Anastase Nduwayezu, Déo Kantungeko, Nicolas Niko, Guy Blomme, James Legg und Jürgen Kroschel. „Farmer Reported Pest and Disease Impacts on Root, Tuber, and Banana Crops and Livelihoods in Rwanda and Burundi“. Sustainability 11, Nr. 6 (15.03.2019): 1592. http://dx.doi.org/10.3390/su11061592.
Der volle Inhalt der QuelleNesamari, R., T. A. Coutinho und J. Roux. „Diseases and pests of Encephalartos species in South Africa“. South African Journal of Botany 98 (Mai 2015): 214. http://dx.doi.org/10.1016/j.sajb.2015.03.168.
Der volle Inhalt der QuelleMontemayor, S. I., P. M. Dellapé und M. C. Melo. „Predicting the potential invasion suitability of regions to cassava lacebug pests (Heteroptera: Tingidae: Vatiga spp.)“. Bulletin of Entomological Research 105, Nr. 2 (19.12.2014): 173–81. http://dx.doi.org/10.1017/s0007485314000856.
Der volle Inhalt der QuelleKwibuka, Yves, Espoir Bisimwa, Arnaud G. Blouin, Claude Bragard, Thierry Candresse, Chantal Faure, Denis Filloux et al. „Novel Ampeloviruses Infecting Cassava in Central Africa and the South-West Indian Ocean Islands“. Viruses 13, Nr. 6 (29.05.2021): 1030. http://dx.doi.org/10.3390/v13061030.
Der volle Inhalt der QuelleBoykin, Sseruwagi, Alicai, Ateka, Mohammed, Stanton, Kayuki et al. „Tree Lab: Portable genomics for Early Detection of Plant Viruses and Pests in Sub-Saharan Africa“. Genes 10, Nr. 9 (21.08.2019): 632. http://dx.doi.org/10.3390/genes10090632.
Der volle Inhalt der QuelleBoykin, Laura, Ammar Ghalab, Bruno Rossitto De Marchi, Anders Savill, James M. Wainaina, Tonny Kinene, Stephen Lamb et al. „Real time portable genome sequencing for global food security“. F1000Research 7 (18.07.2018): 1101. http://dx.doi.org/10.12688/f1000research.15507.1.
Der volle Inhalt der QuelleMoodley, Vaneson, Augustine Gubba und Paramu L. Mafongoya. „Emergence and Full Genome Analysis of Tomato Torrado Virus in South Africa“. Viruses 12, Nr. 10 (15.10.2020): 1167. http://dx.doi.org/10.3390/v12101167.
Der volle Inhalt der QuelleEngelbrecht, Gerhard, Sarina Claassens, Charlotte M. S. Mienie und Hendrika Fourie. „South Africa: An Important Soybean Producer in Sub-Saharan Africa and the Quest for Managing Nematode Pests of the Crop“. Agriculture 10, Nr. 6 (22.06.2020): 242. http://dx.doi.org/10.3390/agriculture10060242.
Der volle Inhalt der QuelleGraziosi, Ignazio, Nami Minato, Elizabeth Alvarez, Dung Tien Ngo, Trinh Xuan Hoat, Tin Maung Aye, Juan Manuel Pardo, Prapit Wongtiem und Kris AG Wyckhuys. „Emerging pests and diseases of South-east Asian cassava: a comprehensive evaluation of geographic priorities, management options and research needs“. Pest Management Science 72, Nr. 6 (24.03.2016): 1071–89. http://dx.doi.org/10.1002/ps.4250.
Der volle Inhalt der QuelleSwartz, Alison, Susan Levine, Hanna-Andrea Rother und Fritha Langerman. „Toxic layering through three disciplinary lenses: childhood poisoning and street pesticide use in Cape Town, South Africa“. Medical Humanities 44, Nr. 4 (20.10.2018): 247–52. http://dx.doi.org/10.1136/medhum-2018-011488.
Der volle Inhalt der QuelleDissertationen zum Thema "Cassava – Diseases and pests – South Africa"
Lombard, Lorenzo. „Fungal diseases in Eucalyptus and Acacia nurseries in South Africa“. Diss., University of Pretoria, 2004. http://hdl.handle.net/2263/24484.
Der volle Inhalt der QuelleDissertation (MSc)--University of Pretoria, 2004.
Microbiology and Plant Pathology
Unrestricted
Surridge, Angela Karen Joanna. „Fungi associated with banana leaf diseases in South Africa“. Diss., University of Pretoria, 2002. http://hdl.handle.net/2263/25782.
Der volle Inhalt der QuelleDissertation (MSc (Microbiology))--University of Pretoria, 2002.
Microbiology and Plant Pathology
unrestricted
Mathewson, Johanna. „Die insekplaagkompleks op sitrus te Vaalharts“. Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51706.
Der volle Inhalt der QuelleFull text to be digitised and attached to bibliographic record.
ENGLISH ABSTRACT: The cultivation of citrus in the Vaalharts region is a fairly recent development. With the introduction of this crop, an insect pest complex has also developed in this region. The presence of these pests was studied in eleven orchards, planted with three citrus cultivars and of varying ages, distributed in the 300 square kilometer cultivation area. Each orchard was inspected for the presence of pests by making use of two weekly sampling techniques. Ten of the most important insect pests of citrus in the Vaalharts region are briefly described by refering to their general appearance, life cycles, feeding and pest status and economic threshold. For every pest various control options, including operational systems, crop cultivation, biological and chemical control, are discussed and, where applicable, illustrated by means of graphic presentations. The seasonal presence of the cirtrus pests in the Vaalharts region is tabulated and discussed individually. With these details as background, an insect pest management programme for citrus in the Vaalharts region is compiled.
AFRIKAANSE OPSOMMING: Die verbouing van sitrus in die Vaalhartsgebied is 'n redelik onlangse ontwikkeling. Gepaard met die nuwe gewas het daar ook 'n insekplaagkompleks in die gebied ontstaan. Die voorkoms van die plae is in elt .boorde, beplant met drie sitruskultivars en van verskillende ouderdomme, verspreid in die 300 vierkante kilometer verbouingsareaal, bestudeer. Elk van die boorde is weekliks ondersoek vir die aanwesigheid van plae deur van twee moniteringstegnieke gebruik te maak. Die tien belangrikste insekplae van sitrus in die Vaalhartsgebied word kortliks beskryf deur na hulle algemene voorkoms, lewenssiklus, voeding en plaagstatus en ekonomiese drempelwaardes asook die moniteringsmetodes wat gebruik is, te verwys. Vir elke plaag word beheeropsies, wat operasionele stelsels, gewasverbouing, bloloqlese en chemiese beheer insluit, bespreek wat, waar toepaslik, aan die hand van grafiese voorstellings gemustreer word. Die seisoenale aanwesigheid van die sitrusplae word in 'n tabel aangedui en individueel bespreek. Met die gegewens as agtergrond is 'n insekplaagbestuurprogram vir sitrus in die Vaalhartsgebied opgestel.
Jacobs, Rene. „Characterisation of Botryosphaeria species from mango in South Africa“. Diss., University of Pretoria, 2002. http://hdl.handle.net/2263/28434.
Der volle Inhalt der QuelleGilbert, Martin Jeffray. „The ecology of the South African citrus thrips, Scirtothrips aurantii Faure and its economic implications“. Thesis, Rhodes University, 1993. http://hdl.handle.net/10962/d1005358.
Der volle Inhalt der QuelleDe, Koker Wenhelene Crystal. „Molecular characterization of grapevine virus E in South Africa“. Thesis, Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/71709.
Der volle Inhalt der QuelleENGLISH ABSTRACT: Grapevine virus E (GVE) is a newly identified virus that has been detected in an established vineyard in South Africa. This virus is a member of the genus Vitivirus, family Flexiviridae. Members of this genus are known to infecte grapevine and are associated with various disease complexes, such as the Rugose wood complex (RWC) and Shiraz disease (SD). However, the role and impact of GVE in South African vineyards are still unknown. It is important to study these viruses to determine how they infect and the possible impact they may have on vine health. The accurate and early detection of grapevine viruses is the first important step in disease management. In this study, reverse transcription-polymerase chain reaction (RT-PCR), double antibody sandwich enzyme linked immunesorbent assay (DAS-ELISA) and quantitative (q)RT-PCR were used for the detection of GVE in the vineyard (Vitis vinifera cv Merlot) where GVE was first identified in South Africa. Reverse transcription-PCR was used for detection and determining the incidence of GVE. The incidence was as low as 3% in the vineyard surveyed. All the GVE positive plants were co-infected with GLRaV-3 and no disease association could therefore be made. Evaluation of the Bioreba Grapevine virus A (GVA) DAS-ELISA kit showed that it did not detect GVE. No cross-reactivity occurred with epitopes of GVE, confirming this kit to be a valid and specific assay for GVA infection. The relative virus titer of GVE was calculated over the growing season of 2010/2011, using qRT-PCR. No fluctuation in virus titer was observed during that growing season. Transmission experiments were performed in an attempt to transfer GVE from grapevine to an alternative host. Three different transmission buffers as well as nine different herbaceous plant species, that have shown to be susceptible to several plant viruses in previous studies, were evaluated. In these experiments, GVE could not be transmitted to any of the herbaceous species. To further characterize GVE, chimeric clones were constructed with GVA. The ORF2 and ORF5 of GVE were cloned into previously constructed GVA ORF2 and ORF5 deletion mutants. Construction of the chimeric clones, 35S-GVA-GR5-ΔORF2-GVE-ORF2 and 35S-GVA-118-ΔORF5-GVE-ORF5 were successful and they were evaluated for their infectivity in N. benthamiana. The 35S-GVA-GR5-ΔORF2-GVE-ORF2 chimera was able to infect and replicate in these plants and disease symptoms such as yellowing of veins and leaf curling were observed. Virus, derived from this vector, was detected by TPIA, RT-PCR and DAS-ELISA. The 35S-GVA-118-ΔORF5-GVE-ORF5 chimeric vector was not able to infect N. benthamiana as no disease symptoms were observed in any of the infiltrated plants and virus was not detected with serological analysis and RT-PCR. This study was aimed at further characterizing the recently identified virus GVE. Here, insight is given into the prevalence of this virus in the vineyard where it was first identified and attempts to biologically characterize GVE were made.
AFRIKAANSE OPSOMMING: Grapevine virus E (GVE) is „n nuut geïndetifiseerde virus wat onlangs in „n gevestigde wingerd in Suid Afrika opgespoor is. Hierdie virus vorm deel van die genus Vitivirus, familie Betaflexiviridae. Spesies in hierdie genus is bekend vir wingerdinfeksies en word met „n verskeidenheid wingerd siektes geassosieer, soos bv. Rugose wood complex (RWC) en Shiraz siekte (SD). Die rol en impak van GVE is nog onbekend. Dit is dus belangrik om die virus te bestudeer om te bepaal hoe dit infekteer en of dit enige impak het op wingerd gesondheid. Akkurate en vroeë opsporing van virusse is die eerste belangrike stap vir virussiekte beheer. In hierdie studie word tru-transkripsie (TT) – polimerase ketting reaksie (PKR), dubbel teenliggaam (DAS) -ensiem gekoppelde immuno-absorberende analise (ELISA) en qTT-PKR gebruik vir die opsporing van GVE in die wingerd (Vitis vinifera cv Merlot) waar dit vroeër in Suid Afrika geïdentifiseer was. Vir opsporing en bepaling van verspreiding is TT-PKR gebruik. Daar is bepaal dat 3% van die wingerd met GVE geïnfekteer is. Al die GVE-positiewe stokke het ook positief getoets vir GLRaV-3 en geen assosiasie met siekte simptome kon gemaak word nie. Evaluering van die Bioreba GVA DAS-ELISA met GVE positiewe stokke het nie GVE opgespoor nie. Geen kruisreaktiwiteit het plaasgevind met epitope van GVE nie en dus is die DAS-ELISA ʼn betroubare toets vir GVA infeksie. Die relatiewe virus titer van GVE was ook bepaal oor die groeiseisoen van 2010/2011 deur qTT-PKR te gebruik. Geen fluktuasie in virus titer gedurende die groeiseisoen is waargeneem nie. Transmissie eksperimente is gedoen om GVE vanaf wingerd na ʼn alternatiewe gasheer oor te dra. Drie verskillende transmissie buffers en tien verskillende sagteplant spesies, wat voorheen vatbaarheid vir plantvirusse getoon het, is gebruik. In die transmissie eksperimente kon GVE nie na enige van die sagteplante oorgedra word nie. Om GVE verder te karakteriseer is hibried-virusse met GVA gemaak. Die leesraam (ORF) 2 en ORF5 van GVE gekloneer in GVA ORF2 en -ORF5 delesie konstrukte, 35S-GVA-GR5-ΔORF2 en 35S-GVA-118-ΔORF5, onderskeidelik (Blignaut, 2009; Du Preez, 2010). Klonering van die hibried konstrukte, 35S-GVA-GR5-ΔORF2-GVE-ORF2 en 35S-GVA-118-ΔORF5-GVE-ORF5, was suksesvol en is in N. benthamiana geëvalueer. Virus afkomstig van die 35S-GVA-GR5-ΔORF2-GVE-ORF2 hibried konstruk, kon plante suksesvol infekteer en kon repliseer binne hierdie plante. Siektesimptome soos vergeling van die are en rolblaar is ook waargeneem in plante geïnfekteer met hierdie hibried konstruk. Plante is getoets met weefsel afdruk immuno analise (TPIA), TT-PKR en DAS-ELISA en is positief gevind vir virus afkomstig van hierdie konstruk. Die 35S-GVA-118-ΔORF5-GVE-ORF5 hibried kon nie N. benthamiana infekteer nie en geen siektesimptome is waargeneem in enige van die plante geïnfiltreer met hierdie konstruk. Serologiese analise en TT-PKR het ook nie virus in die N. benthamiana plante opgespoor nie. Die doel van hierdie studie was om GVE te karakteriseer. In hierdie studie word insig gegee oor die verspreiding van hierdie virus in Suid Afrika en pogings is gemaak om GVE biologies te karakteriseer.
Rentel, Monique. „Morphology and taxonomy of tortricid moth pests attacking fruit crops in South Africa“. Thesis, Stellenbosch : Stellenbosch University, 2013. http://hdl.handle.net/10019.1/79825.
Der volle Inhalt der QuelleENGLISH ABSTRACT: Cydia pomonella (codling moth), Thaumatotibia leucotreta (False codling moth), Thaumatotibia batrachopa (Macadamia nut borer), Grapholita molesta (Oriental fruit moth), Cryptophlebia peltastica (Litchi moth), Epichoristodes acerbella (Pear leafroller/Carnation worm) and Lozotaenia capensana (Apple leafroller) are the most economically important tortricids affecting various crops in South Africa. The correct identification of these species, especially of the larval stage, is of great importance in pest management. Using available literature, augmented by additional morphological studies, an interactive identification key (Lucid key) for larval and adult stages of the seven species was developed. The colour and markings of the head, characteristics of the prothoracic and anal shields, the position of the prespiracular setae (L-group) relative to the spiracle on the prothoracic segment, the position of the spiracle on the eighth abdominal segment and L-group on the ninth abdominal segment, as well as the presence or absence of the anal comb are key characteristics for larval identification. For adult identification, wing pattern and genitalia are the most important features. However, the use of genitalia for moth identification might be difficult for the lay user, as the dissection and mounting of these structures requires certain skills and specialized equipment. Thus, genitalia have not been included in the Lucid Key. Differences in the morphological characteristics of most pupae were so minute that this stage was also not included in the Lucid key. However, the pupae of E. acerbella and L. capensana are easily distinguished from those of the other species by the presence of acremaster. This study also included the first morphological description of the pupa of L. capensana, which can be distinguished from that of E. acerbella by various features of the cremaster, antennae, spiracle shape, number of setae on abdominal segments A5-7, the size of spines on A3-7, and the presence/absence of spines on A9. A previous study by Timm (2005) indicated that geographically isolated populations of T. leucotreta tend to be genetically distinct. This raised the question of whether speciation/subspeciation has occurred or is occurring. Male moth genitalia are thought to evolve rapidly and are often the only features that can reliably distinguish similar species. Hence, variation in the shape of the valvae of T. leucotreta was used to determine whether divergence has occurred between populations of T. leucotreta. Elliptical Fourier analysis was used to analyze the valvar variation in three different populations. Although some variation in valvar shape was detected among mean population values for certain traits, no clear pattern emerged. Principle component analysis also showed no distinct clustering of valvae shape among populations, providing no evidence for divergence in male genitalia and therefore no morphological evidence of incipient speciation.
AFRIKAANSE OPSOMMING: Cydia pomonella (Kodlingmot), Thaumatotibia leucotreta (Valskodlingmot), T. batrachopa (Makadamianeutboorder), Grapholita molesta (Oosterse vrugtemot), Cryptophlebia peltastica (Lietsjiemot), Epichoristodes acerbella (Peerbladroller/Angelierrusper) en Lozotaenia capensana (Appelbladroller) is die mees ekonomies belangrike tortrisiede van die vrugtebedryf in Suid-Afrika. Die juiste identifikasie van hierdie spesies, veral van hulle larwale stadium, is van groot belang by plaagbestuur. Deur gebruik te maak van beskikbare literatuur, aangevul deur bykomstige morfologiese studies, is ‗n interaktiewe uitkenningssleutel (―Lucid key‖) vir die larwale en volwasse stadia van die sewe spesies ontwikkel. Die kleur en tekening van die kop, kenmerke van die prothorakale en anale skild, die ligging van die prespirakulêre setae (L-groep) relatief tot die spiraculum op die prothorakale segment, die ligging van die spirakulum op die agste abdominale segment en L-groep op die negende abdominale segment, asook die aan- of afwesigheid van die anale kam is sleutel kenmerke vir larwale uitkenning. Vir die volwassenes is die vlerktekening en genitalia die mees belangrike kenmerke. Die gebruik van die genitalia vir motuitkenning kan egter vir die leek gebruiker moeilik wees omdat die disseksie en montering van hierdie strukture bepaalde vaardighede en gespesialiseerde toerusting vereis. Vir die rede is die genitalia nie in die Lucid-sleutel ingesluit nie. Verskille in die morfologiese kenmerke van meeste papies is klein en die stadium is gevolglik ook nie in die sleutel ingesluit nie. Die papies van E. acerbella en L. capensana kan egter maklik van die ander spesies onderskei word deur die aanwesigheid van ‗n cremaster. Hierdie studie sluit ook die eerste morfologiese beskrywing van die papie van L. capensana in, wat van dié van E. acerbella onderskei kan word deur gebruik te maak van kenmerke van die cremaster, antennae, spirakulêre vorm, aantal setae op abdominale segmente A5-7, die grootte van stekels op A3-7, en die aan- of afwesigheid van stekels op A9. ‗n Vroeëre studie (Timm 2005) het aangedui dat geografies geïsoleerde bevolkings van T. leucotreta neig om geneties verskillend te wees. Dit het die vraag laat ontstaan of spesiasie/subspesiasie moontlik plaasgevind het of steeds plaasvind. Manlike mot genitalië word geag om vinnig te ontwikkel en is dikwels die enigste kenmerke wat betroubaar tussen soortgelyke spesies kan onderskei. Dus is die variasie in die vorm van die valvae van T. leucotreta gebruik om te bepaal of divergensie wel tussen bevolkings van T. leucotreta plaasgevind het. Elliptiese Fourier ontleding is gebruik om die valvae se variasie by drie verskillende bevolkings te ontleed. Alhoewel enkele variasie in die vorm van die valvae bespeur is by die gemiddelde bevolkingswaardes vir bepaalde eienskappe, kon geen duidelike patroon bespeur word nie. Hoofkomponentontleding het ook geen duidelike groepering van valvae se vorm tussen bevolkings getoon nie, wat geen bewys lewer van divergensie in die manlike genitalia en dus geen morfologiese bewys van beginnende spesiasie.
Schreuder, Wouter. „Characterization and pathogenicity of South African isolates of Fusarium oxysporum f. sp. melonis“. Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51651.
Der volle Inhalt der QuelleENGLISH ABSTRACT: The purpose of this study was to characterize the race and vegetative compatibility of Fusarium oxysporum f. sp. melonis (FOM) isolates collected in the major melon producing areas, to report on their geographical distribution, and their possible relatedness to isolates from other countries. Seventy two FOM isolates obtained from 30 fields in 17 melon producing regions were race-typed using the differential cultivars Topmark (susceptible to all races), Doublon (Fomi), CM 17187 (Fom2) and Perlita (Fom3) and grouped by means of vegetative compatibility. All isolates belonged to vegetative compatibility group 0134, indicating a high degree of genetic homogeneity among the South African FOM population. Fifty four isolates were identified as race 0, eight as race 1, and 10 as race 2. Race 0 occurred in 15 of the regions whereas race 1 was sporadically recovered. Race 2, on the other hand, was obtained only from four fields located in one geographical region. Perlita plants (carrying the gene Fom3) inoculated with local isolates ofrace 0 and race 2 and reference isolates of race 0 became stunted, their leaves turned yellow, and became thickened and brittle. These results suggested that Fom3 in Perlita confers a tolerant reaction compared to the resistant reaction of gene FornI in Doublon. The disease reaction of cultivar Perlita to FOM was therefore reinvestigated. Twenty isolates, including the four FOM races (0, 1, 2, and 1,2) obtained from different countries, were used. The differential cultivars were included to verify virulence of the isolates. Perlita plants inoculated with three isolates of race 2 remained asymptomatic. The remaining race 2 and 0 isolates, induced severe stunting of Perlita plants, but mean percentage stunting values did not differ significantly (P = 0.05) and ranged between 25.1 and 50.0. Leaves of stunted plants were chlorotic, thickened and brittle. Disease reaction of Perlita was verified at a lower inoculum concentration with two race 2 (pipette method) and two race 0 isolates (root dip method). Results proved that Fom3 does not confer similar resistance towards race 0 and some race 2 isolates as FornI in Doublon. Cultivars possessing Fom3, should therefore be considered tolerant to FOM races 0 and 2. The ability of a nit mutant isolate, generated from FOM race 0 which belongs to VCG 0134, to change its virulence during infection of melon plants, was investigated under quarantine. Seedlings of melon cultivars Imperial 45 and Early Sweet (no resistance genes), Amber (Fom2) and Fiata (FomI, Fom2) were consecutively grown in two cement troughs in a gauzehouse. Each planting was terminated when plants had advanced Fusarium wilt or after the fruit were harvested. In the first planting, Imperial 45 seedlings were transplanted and artificially inoculated with the nil mutant isolate. In the consecutive plantings, seeds were sown in the infested soil to enable natural infection. For each crop, representative plants showing Fusarium wilt were selected for isolation. All F. oxysporum isolates recovered were single-spored and their nit mutant and VCG status verified. Virulence of the labelled isolates was determined using differential cultivars. In trough A, all plants of the susceptible cultivars Imperial 45 and Early Sweet crops showed Fusarium wilt. The labelled isolates recovered from the selected plants were all designated race O. In the first crop (planting No.5) of the resistant cultivar Amber, 6.7% of the plants developed Fusarium wilt. In the second Amber crop the disease incidence increased to 56.6%, and to 81.8% in the final crop. Contrary to the susceptible cultivars, only race 2 isolates were obtained from the symptomatic Amber plants. Similar data were found with the susceptible cultivar Imperial 45 and the resistant cultivar Amber in trough B. Planting of Fiata caused a dramatic reduction in Fusarium wilt incidence in trough B. However, 1.2% of plants were affected by Fusarium wilt in the first Fiata crop (planting No.6), whereas 4% of the plants were symptomatic in the final planting. From these symptomatic Fiata plants only race 1,2 isolates were obtained. These findings, and the fact that the symptomatic plants represented a substantial proportion of the first Amber (approximately 7-15%) and Fiata (approximately 2%) crops, provedthat changes in the race structure of this fungal pathogen occurred rapidly when confronted with a resistant cultivar. The potential of RAPD analysis to differentiate between the isolates displaying virulence changes was evaluated. Four F. oxysporum f. sp. niveum isolates were included as an outgroup. A histopathological study was conducted to verify whether these isolates retain their ability to behave as true vascular pathogens. The three primers used clearly distinguished the 12 FOM isolates from the four F. oxysporum f. sp. niveum isolates. However, the primers showed a highly conserved and characteristic banding pattern for the FOM isolates which represented three physiological races (race 0, race 2, race 1,2), indicating that RAPD analysis cannot detect race-specific groupings in FOM. Disease reactions on the three differential cultivars confirmed the virulence of FOM isolates. The histopathological data furthermore proved that the two FOM races (race 2, race 1,2), which derived from the race 0 parent isolate, retained their ability to behave as true vascular pathogens.
AFRIKAANSE OPSOMMING: DIE KARAKTERISERING EN PATOGENESITEIT VAN SUID-AFRIKAANSE ISOLATE VAN FUSARIUMOXYSPORUMF. SP.MELONIS Die doel van die studie was om Fusarium oxysporum f. sp. melonis (FOM) isolate wat in die hoof spanspekproduserende gebiede versamel is, volgens ras en vegetatiewe verenigbaarheid te karakteriseer, en hul geografiese verspreiding en verwantskap met isolate van ander lande aan te dui. Twee en sewentig FOM isolate afkomstig vanaf 30 landerye wat 17 spanspekproduserende areas verteenwoordig, is gebruik. Die differensiële kultivars Topmark (vatbaar vir alle rasse), Doublon (Forni), CM 17187 (Fom2) en Perlita (Fond) is gebruik om die rasbepalings te doen asook om die vegetatiewe verenigbare groepe (VVG) te bepaal. Al die isolate is as VVG 0134 geklassifiseer, wat 'n hoë mate van genetiese homogenesiteit binne die Suid-Afrikaanse populasie aandui. Vier en vyftig isolate is as ras 0, agt as ras 1 en 10 as ras 2 geklassifiseer. Ras 0 is vanaf 15 gebiede afkomstig, terwyl ras 1 sporadies voorgekom het. Ras 2 is vanuit vier landerye binne dieselfde geografiese gebied verkry. Plante van die kultivar Perlita wat met plaaslike isolate van ras 0 en 2, asook verwysings-isolate van ras 0 geïnokuleer is, het verdwerg voorgekom. Die blare van die plante het vergeel, verdik en bros voorgekom. Hierdie siekte reaksie het aangedui dat Fond in Perlita toleransie bewerkstellig in teenstelling met die weerstandbiedende reaksie van geen Fomi in Doublon. Die siekte reaksie van Perlita teenoor FOM is dus verder ondesoek. Hiervoor is 20 isolate wat al vier FOM rasse insluit (0, 1, 2, en 1,2), en van verskillende wêrelddele afkomstig is, gebruik. Die virulensie van die isolate is met die differensiële kultivars bevestig. Drie van die ras 2 isolate het geen siektesimptome op Perlita veroorsaak nie. Die ander ras 2 isolate, en al die ras 0 isolate, het egter die Perlita plante aansienlik verdwerg en die blare vergeel en verdik. Laasgenoemde groep isolate het 'n gemiddelde verdwergingsindeks van tussen 25.1% en 50.0% veroorsaak. Die siekte reaksie by Perlita is verder bevestig deur plante teen 'n laer inokulumdigtheid van twee ras 2 (pipet metode), en twee ras 0 (wortel-doop metode) isolate, te inokuleer. Uit die resultate was dit duidelik dat die weerstand wat Fom3 teenoor ras 0 en sommige ras 2 isolate verskaf, van FornI verskil. Kultivars wat oor die weerstandsgeen Fom3 beskik moet dus as tolerant beskou word. 'n Ondersoek is geloods na die vermoë van 'n nil mutant isolaat, genereer vanaf die wilde ras 0 isolaat van FOM (VVG 0134), om onder kwarantyn sy virulensie gedurende infeksie van spanspekplante te verander. Saailinge van die spanspekkultivars Early Sweet (geen weerstandsgene), Amber (Fom2) en Fiata (FornI, Fom2) is opeenvolgens in twee sement trêe in 'n gaashuis verbou. Die afsonderlike aanplantings is beëindig sodra gevorderde Fusarium-verwelksimptome verkry is, of nadat vrugte ge-oes is. Vir die eerste aanplanting is oorgeplante Imperial 45 saailinge kunsmatig met die nil mutant isolaat geïnokuleer. Tydens die opeenvolgende aanplantings is saad direk in die besmette grond gesaai ten einde natuurlike infeksie te verkry. Met elke aanplanting is isolasies gedoen vanaf verteenwoordigende plante wat Fusarium-verwelksimptome getoon het. Alle F. oxysporum isolate wat verkry is, is ge-enkelspoor en hul nit mutant status en VVG is bevestig. Virulensie van die gemerkte isolate is bepaal deur inokulasie van die differensiële kultivars. Alle plante van die vatbare Imperial 45 en Early Sweet kultivars wat in trog A geplant is, het Fusarium-verwelksimptome getoon. Die gemerkte isolate wat vanaf die verteenwoordigende plante verkry is, is almal as ras 0 geklassifiseer. Tydens die eerste aanplanting van die weerstandbiedende kultivar, Amber (aanplanting No.5), het 6.7% van die plante Fusarium-verwe1ksimptome ontwikkel. Tydens die tweede en derde aanplanting van Amber het die frekwensie van siektevoorkoms verhoog na 56.6% en 81.8 %, onderskeidelik. In teenstelling met die vatbare kultivars, is slegs ras 2 vanuit die Amber plante met siektesimptome verkry. Soortgelyke resultate is met Imperial 45 en Amber in trog B verkry. Aanplanting van kultivar Fiata het egter 'n dramatiese verlaging in die voorkoms van Fusarium-verwelk bewerkstellig. Tydens die eerste Fiata aanplanting (aanplanting No.6) het 1.2% plante Fusarium-verwelksimptome ontwikkel, en 4% tydens die laaste aanplanting. Vanaf hierdie plante is slegs ras 1,2 isolate verkry. Hierdie bevindings, en die feit dat 'n aansienlike hoeveelheid van die Amber (ongeveer 7-15%) en Fiata plante (ongeveer 2%) siektesimptome getoon het, bewys dat FOM vinnig van virulensie verander wanneer die patogeen 'n weerstanbiedende kultivar infekteer. Die vermoë van RAPD analise om tussen isolate wat in virulensie verander het, te onderskei, is ondersoek. Vier isolate van F. oxysporum f. sp. niveum is as 'n buite-groep ingesluit. Om te bevestig dat die isolate wat van ras verander het wel egte vaskulêre patogene is, is 'n histopatologiese ondersoek gedoen. Die drie inleiers wat gebruik is, het die 12 FOM isolate duidelik van die vier F. oxysporum f. sp. niveum isolate onderskei. Die 12 FOM isolate wat drie fiosologiese rasse (ras 0, ras 2, ras 1,2) verteenwoordig het, is egter saam gegroepeer, wat aandui dat hierdie metode nie tussen rasse van FOM kan onderskei nie. Inokulasiestudies met die differensiële kultivars het die virulensie van die isolate bevestig. Die histopatologiese ondersoek het verder bewys dat beide FOM rasse (ras 2, ras 1,2) wat vanaf die wilde tipe ras ° isolaat ontstaan het, hul vermoë behou het om as egte vaskulêre patogene op te tree.
De, Villiers M. (Marelize). „Die gebruik van 'n swaainet vir die monitering en diversiteitsbepaling van insekte op lusern in die Wes-Kaap“. Thesis, Stellenbosch : Stellenbosch University, 2002. http://hdl.handle.net/10019.1/52775.
Der volle Inhalt der QuelleENGLISH ABSTRACT: Lucerne is the most important pasture and fodder crop in the winter rainfall area of South Africa. Various pests are known to cause damage to this crop. The use of the sweep net for monitoring pests is a cheap, easy and quick technique. If the sweep net is suitable for the lucerne pests in South Africa, potential pest status can be determined easily and quickly and the necessary precautionary measures taken to prevent crop losses. From a managerial point of view, it is also important to know the composition of the insect community in order to follow practices in which the number of beneficial insects can be increased and the injurious insects decreased. Therefore a study was done to quantify the use of the sweep net as a survey technique for monitoring pests on established lucerne stands. Insect diversity was also determined to obtain information on the insect families and guilds on lucerne. The redlegged earth mite, due to its importance as a pest, and the Anystis mite, important as a predator, were also included. The sweep net proved to be suitable for the sampling of the main lucerne pests. If a 29 cm diameter sweep net is swiped once per pace for six long paces, twelve systematically chosen sampling units are recommended for the lucerne earth flea and aphids. It is not necessary to differentiate amongst the three aphid species, or between the winged and unwinged aphids. Actual counts should be used instead of absence-presence data. Instead of counting all the insects in a sample, sub-samples can be taken. Operational characteristic curves can be used to determine the risk involved in the decision not to intervene, for example by spraying or grazing. Recommendations for monitoring and the accuracy of control decisions for the redlegged earth mite, Sitona weevil and lucerne butterfly can only be made after threshold values have been determined. The pea aphid, bluegreen aphid and lucerne earth flea showed peaks in their population levels during spring. Peak numbers of the spotted alfalfa aphid occurred during late summer and autumn. The Sitona weevil and lucerne butterfly numbers reached peak levels during late spring and early summer. For all pests population levels were dramatically reduced after grazing or cutting of the plantings. Therefore, these cultivation practices provided good control. The herbivores made up more than 85% of the insect community in lucerne. The largest herbivorous families, in terms of the number of individuals per family, were the Aphididae and Sminthuridae. These two families contain the main lucerne pests, the pea aphid, bluegreen aphid, spotted alfalfa aphid and the lucerne earth flea. The largest predatory family was the Anystidae, represented by the Anystis mite, the most important predator of the red legged earth mite and lucerne earth flea. Another well represented predatory family was the Coccinellidae, containing natural enemies of the aphids. The dryland plantings had a higher percentage of predators than the irrigated lucerne. The most important parasitaids were those in the superfamily Chalcidoidea and in the family Braconidae. The main detritivores were springtails in the suborder Arthropleona, insects in the families Mycetophilidae on irrigated lucerne, and Mycetophagidae on dryland lucerne. The most abundant visitors were in the families Chironomidae, Drosophilidae and Tephritidae. The dryland plantings had a lower percentage of visitors than the irrigated plantings. The number of insect families, as well as the number of individuals per family, was lower at the dryland plantings than at the irrigated plantings. The vast majority of insect families found on lucerne were collected during the one-year sampling period. A lower diversity was found where grazing was more severe, and there was a negative relationship between diversity and evenness.
AFRIKAANSE OPSOMMING: Lusern is die belangrikste wei- en voergewas 10 die winterreëngebied van Suid- Afrika. Hierdie gewas word deur 'n verskeidenheid plae aangeval. Die gebruik van die swaainet vir die monitering van plae is 'n goedkoop, maklike en vinnige tegniek. lndien die swaainet geskik is vir die betrokke plae in Suid-Afrika, kan potensiële plaagstatus van die plae dus maklik en vinnig bepaal word en die nodige voorsorgmaatreëls getref word om verliese te voorkom. Vanuit 'n bestuursoogpunt is dit ook belangrik om te weet wat die samestelling van die insekgemeenskap is sodat praktyke gevolg kan word waardeur die getal voordelige insekte verhoog en nadelige insekte verlaag word. Gevolglik is 'n studie uitgevoer om die gebruik van die swaainet te kwantifiseer as 'n monsternemingsmetode vir die monitering van plae op gevestigde lusernstande. Insekdiversiteit is ook bepaal ten einde inligting te bekom oor die insekfamilies en -gildes op lusern. Die lusernerdvlooi en swartsandmyt, vanweë hul belang as plae, en die Anystis-roofmyt, vanweë sy belang as predator, is ook ingesluit. Die swaainet blyk geskik te wees vir die monitering van die. vernaamste lusernplae. Wanneer 'n 29 cm deursnee swaainet vir ses lang treë een keer per tree geswaai word, word 12 sistematies gekose steekproefnemingseenhede vir die lusernerdvlooi en plantluise aanbeveel. Daar hoef nie onderskeid tussen die plantluisspesies en tussen gevleuelde en ongevleuelde plantluise getref te word nie. Daar moet gebruik gemaak word van werklike insektellings en nie van aanwesigheid-afwesigheid data nie. In plaas van om al die insekte in 'n monster te tel, kan submonsters geneem word. Operasionele karakteristieke kurwes kan gebruik word om die risiko verbonde aan die besluit om nie op te tree, deur byvoorbeeld te spuit of bewei nie, te bepaal. Vir die swartsandmyt, Sitona-snuitkewer en lusernskoenlapper moet drempelwaardes eers vasgestel word voordat aanbevelings vir monitering en die akkuraatheid van besluite rakende beheer, gegee kan word. Vir die ertjieluis, blougroenluis en lusernerdvlooi het die bevolkingsvlakke 'n piek in die lente bereik. Die gevlekte lusernluis se piekgetalle was hoofsaaklik in die laat somer en herfs. Die Sitona-snuitkewer en lusernskoenlapper het piekgetalle gehad in die laat lente en vroeë somer. Vir al die plae het bevolkingspieke drasties afgeneem nadat die aanplantings bewei of gesny is. Hierdie verbouingspraktyke blyk dus goeie beheer te verskaf. Die herbivore op lusern het meer as 85% van die insekgemeenskap beslaan. Die grootste herbivoorfamilies, in terme van aantal individue per familie, was die Aphididae en Sminthuridae. Hierdie twee families bevat die vernaamste lusernplae, naamlik die ertjieluis, blougroenluis, gevlekte lusernluis en lusernerdvlooi. Die grootste predatoriese familie was die Anystidae, wat verteenwoordig is deur die Anystis-roofmyt. 'n belangrike predator van die swartsandmyt en lusernerdvlooi. Nog 'n predatoriese familie wat goed verteenwoordig was, was die Coccinellidae, natuurlike vyande van plantluise. Die droëland aanplantings het 'n hoër persentasie predatore gehad as die besproeide lusern. Die belangrikste parasitoïede aanwesig was dié in die superfamilie Chalcidoidea en familie Braconidae. Die vernaamste detritivore was erdvlooie in die suborde Arthropleona, insekte in die families Mycetophilidae by besproeide lusern, en Mycetophagidae by droëland lusern. Die volopste besoekers was lede van die families Chironomidae, Drosophilidae en Tephritidae. Die droëland aanplantings het 'n laer persentasie besoekers gehad as die besproeide lusern. Die aantal insekfamilies, asook die aantal individue per familie, was laer by die droëland aanplantings as by die besproeide aanplantings. Die oorgrote meerderheid insekfamilies wat op lusern voorkom, is gedurende die een jaar opnameperiode waargeneem. 'n Laer insekdiversiteit is gevind waar beweiding strawwer was, en daar was 'n negatiewe verband tussen diversiteit en gelykmatigheid.
Nepgen, Eugene Stephan. „A study on the application technology of the sterile insect technique, with focus on false codling moth, Thaumatotibia leucotreta (Meyrick) (Lepidoptera: Tortricidae), a pest of citrus in South Africa“. Thesis, Rhodes University, 2014. http://hdl.handle.net/10962/d1013199.
Der volle Inhalt der QuelleBücher zum Thema "Cassava – Diseases and pests – South Africa"
Ojo, Bamidele. The man, John Steve Yaninek: A unique biological control scientist America has ever produced : a unique fortune to Africa and a peep into environmentally sustainable cassava plant protection. Oyo State, Nigeria: Starlight Press, 1997.
Den vollen Inhalt der Quelle findenSwain, V. M. A list of phytophagous insects and mites on forest trees and shrubs in South Africa. Pretoria: Dept. of Agriculture and Water Supply, 1986.
Den vollen Inhalt der Quelle findenIntegrating the management of pests, weeds and diseases of cassava in Africa. Kampala: African Crop Science Society, 1994.
Den vollen Inhalt der Quelle findenWalters, Dale. Chocolate Crisis. University Press of Florida, 2021. http://dx.doi.org/10.5744/florida/9781683401674.001.0001.
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