Refine
Document Type
- Article (5) (remove)
Has Fulltext
- yes (5)
Is part of the Bibliography
- no (5)
Keywords
- AFLP (5) (remove)
Background: Hybridisation is presumed to be an important mechanism in plant speciation and a creative evolutionary force often accompanied by polyploidisation and in some cases by apomixis. The Potentilla collina group constitutes a particularly suitable model system to study these phenomena as it is morphologically extensively variable, exclusively polyploid and expresses apomixis. In the present study, the alpine taxon Potentilla alpicola has been chosen in order to study its presumed hybrid origin, identify underlying evolutionary processes and infer the discreteness or taxonomic value of hybrid forms.
Results: Combined analysis of AFLP, cpDNA sequences and ploidy level variation revealed a hybrid origin of the P. alpicola populations from South Tyrol (Italy) resulting from crosses between P. pusilla and two cytotypes of P. argentea. Hybrids were locally sympatric with at least one of the parental forms. Three lineages of different evolutionary origin comprising two ploidy levels were identified within P. alpicola. The lineages differed in parentage and the complexity of the evolutionary process. A geographically wide-spread lineage thus contrasted with locally distributed lineages of different origins. Populations of P. collina studied in addition, have been regarded rather as recent derivatives of the hexaploid P. argentea. The observation of clones within both P. alpicola and P. collina suggested a possible apomictic mode of reproduction.
Conclusions: Different hybridisation scenarios taking place on geographically small scales resulted in viable progeny presumably stabilised by apomixis. The case study of P. alpicola supports that these processes played a significant role in the creation of polymorphism in the genus Potentilla. However, multiple origin of hybrids and backcrossing are considered to produce a variety of evolutionary spontaneous forms existing aside of reproductively stabilised, established lineages.
In Western Europe pedunculate oak (Quercus robur L.) is the forest tree with the highest number of phytophagous insect species (Yela & Lawton 1997). One of these, the green oak leaf roller Tortrix viridana L. is an oligophagous herbivorous moth with a host range limited to the genus Quercus (Hunter 1990, Du Merle 1999). During outbreaks, T. viridana often leads to defoliation of oaks in spring. The abundance of T. viridana is subject to the population size fluctuations typical for herbivorous insects, where periods of small population sizes (latent periods) alternate with periods of high population sizes (outbreak) (e.g. Schütte 1957, Horstmann 1984). Apart from many experimental studies on population dynamics of the moth (e.g. Hunter 1990, Du Merle 1999, Ivashov & al. 2002) so far little attention has been paid to the genetic variation within the species as an important aspect of the genetics of this host-parasite interaction. Simchuk & al. (1999) found changes in the heterozygosity level of different isozyme loci during outbreaks in T. viridana and molecular markers for T. viridana have been developed for analyses of genetic variation within and among populations (Schroeder & Scholz 2005). But, investigations of genetic variation within and among populations of forest pest species are important to predict future pest outbreaks. So far the processes outbreaks based on are not entirely clarified, however it is known that migration plays a major role. Using molecular markers investigations of the genetic variation are possible and offer the opportunity to analyse distribution events. In this paper first results are presented concerning the genetic variation of the green oak leaf roller at three geographic scales: (1) among trees within a population, (2) among populations at a small spatial scale of about 150 km and (3) among populations at a broader geographic scale up to 3000 km. Furthermore results of the genetic variation of oaks at the small spatial scale are represented.
The codling moth, Cydia pomonella (Lep., Tortricidae), is a significant pest of orchard crops such as apple and pear in Southern Germany, and can cause severe economic damage to apple crops. Due to resistance to conventional pesticides and the growing market for organic fruit, Cydia pomonella Granulovirus (CpGV) has been used to control C. pomonella in Germany for over 10 years. Recently, populations exhibiting resistance to CpGV have been reported. In this study, we have used amplified fragment length polymorphism (AFLP) markers to estimate genetic variations between eight different C. pomonella populations, which were obtained from different locations exhibiting varying levels of resistance to CpGV. Three different AFLP primer combinations generated a total of 194 AFLP fragments, ranging from 57.84 to 424.11 bp, with an average of 59.23 amplified fragments per primer combination. The total number of segregating fragments ranged from 181 to 115 and resulted in a high loci polymorphism of 100% in most cases, except for two populations, where it was found to be 88.1% and 93.3%. An analysis of genetic variation based on the obtained AFLP markers resulted in high gene diversity (Hj) values, ranging between 0.2884 to 0.3508. Hj values also indicated a loss in gene diversity within a population over time. The Wright Fixation Index (FST) values indicated a low to moderate genetic differentiation in the populations. The cluster analysis (UPGMA), based on genetic distance values, showed that the majority of C. pomonella populations from different locations were clearly distributed into distinct groups and showed a large genetic variability.
Die Bergbaufolgelandschaft stellt in Mitteleuropa die einzigartige Möglichkeit dar, den Prozess der Primärsukzession großflächig zu beobachten. Hierbei können z.B. Veränderungen in der Artenanzahl, der Artenzusammensetzung oder in der Struktur der Lebensgemeinschaften untersucht werden. Die bergbauliche Inanspruchnahme der Flächen führt zu einer extremen Störung. Nach erfolgter Verkippung des Abraumes können ökologische Prozesse wie Bodenbildung und Sukzession auf den neu entstandenen Flächen jedoch häufig relativ ungestört ablaufen. Um den Prozess der Besiedlung dieser Flächen zu analysieren, wurde die Laufkäferart Calathus erratus (SAHLBERG, 1827) als Modellart ausgewählt. Mittels genetischer Methoden wurde die Besiedlung großflächiger gestörter Offenlandbereiche im andschaftsmaßstab untersucht. Hierzu wurden Tagebaustandorte verschiedenen Alters und Entfernung zum unverritzten Land als Untersuchungsgebiete gewählt. Als Vergleichsstandorte dienten ehemalige Truppenübungsplätze. Die Käferpopulationen der verschiedenen Untersuchungsstandorte wurden hinsichtlich ihrer genetischen Variabilität mittels molekularer Marker untersucht. Von den genetischen Untersuchungen zur Populationsstruktur der Laufkäferart Calathus erratus werden Rückschlüsse auf die Entwicklung der genetischen Variabilität in gestörten und fragmentierten Landschaften erwartet.
The entomopathogenic hyphomycete Beauveria brongniartii is a promising candidate for biocontrol of economically important agricultural and forest pests. Assessment of genetic relatedness of this species appears to be essential to gain insight into the monitoring of such biocontrol products. Distinction of Beauveria spp. strains with different virulence to target organisms revealed to be a serious constraint in the development of successful biocontrol using these important species. Thus, there is a need to find ways to monitor these strains when applied to natural agents. We have used amplified fragment length polymorphism (AFLPs) markers to estimate genetic variations among fourteen isolates (ten B. brongniartii, two B. bassiana (BALSAMO) VUILLEMIN and two Nomuraea rileyi (FARLOW) SAMSON) obtained from different geographical origins and hosts with differing virulence to scarabs. Seven different AFLP primer combinations yielded a total of 229 AFLP fragments comprised between 30 (EcoRI-ACA/Tru1l-C) to 57 (EcoRI-AAG/Tru1l-CTT) AFLP markers with an average of 54 amplified fragments per primer combination. Fragment size varied between 50-541 base pairs (bp) among the ten B. brongniartii isolates analysed in this study achieving a good resolution between the isolates. The cluster analysis based on genetic distance values clustered all isolates at above 0.40 similarity and demonstrated that some B. brongniartii isolates from distinct geographical origins and various hosts showed a greater genetic variability.