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1.
Ecol Lett ; 15(12): 1439-48, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23006492

ABSTRACT

The Convention on Biological Diversity (CBD) aims at the conservation of all three levels of biodiversity, that is, ecosystems, species and genes. Genetic diversity represents evolutionary potential and is important for ecosystem functioning. Unfortunately, genetic diversity in natural populations is hardly considered in conservation strategies because it is difficult to measure and has been hypothesised to co-vary with species richness. This means that species richness is taken as a surrogate of genetic diversity in conservation planning, though their relationship has not been properly evaluated. We tested whether the genetic and species levels of biodiversity co-vary, using a large-scale and multi-species approach. We chose the high-mountain flora of the Alps and the Carpathians as study systems and demonstrate that species richness and genetic diversity are not correlated. Species richness thus cannot act as a surrogate for genetic diversity. Our results have important consequences for implementing the CBD when designing conservation strategies.


Subject(s)
Biodiversity , Genetic Variation , Plants/genetics , Ecosystem , Geography
2.
J Hered ; 102(4): 479-88, 2011.
Article in English | MEDLINE | ID: mdl-21576288

ABSTRACT

For many applications in population genetics, codominant simple sequence repeats (SSRs) may have substantial advantages over dominant anonymous markers such as amplified fragment length polymorphisms (AFLPs). In high polyploids, however, allele dosage of SSRs cannot easily be determined and alleles are not easily attributable to potentially diploidized loci. Here, we argue that SSRs may nonetheless be better than AFLPs for polyploid taxa if they are analyzed as effectively dominant markers because they are more reliable and more precise. We describe the transfer of SSRs developed for diploid Mercurialis huetii to the clonal dioecious M. perennis. Primers were tested on a set of 54 male and female plants from natural decaploid populations. Eight of 65 tested loci produced polymorphic fragments. Binary profiles from 4 different scoring routines were used to define multilocus lineages (MLLs). Allowing for fragment differences within 1 MLL, all analyses revealed the same 14 MLLs without conflicting with merigenet, sex, or plot assignment. For semiautomatic scoring, a combination of as few as 2 of the 4 most polymorphic loci resulted in unambiguous discrimination of clones. Our study demonstrates that microsatellite fingerprinting of polyploid plants is a cost efficient and reliable alternative to AFLPs, not least because fewer loci are required than for diploids.


Subject(s)
DNA Fingerprinting/methods , Euphorbiaceae/genetics , Genetic Markers/genetics , Genetics, Population/methods , Microsatellite Repeats/genetics , Polyploidy , Amplified Fragment Length Polymorphism Analysis , Base Sequence , Cluster Analysis , DNA Primers/genetics , Genotype , Germany , Molecular Sequence Data , Poland , Polymerase Chain Reaction , Sequence Analysis, DNA
3.
Ann Bot ; 107(6): 1057-61, 2011 May.
Article in English | MEDLINE | ID: mdl-21320876

ABSTRACT

BACKGROUND AND AIMS: The frequency at which males can be maintained with hermaphrodites in androdioecious populations is predicted to depend on the selfing rate, because self-fertilization by hermaphrodites reduces prospective siring opportunities for males. In particular, high selfing rates by hermaphrodites are expected to exclude males from a population. Here, the first estimates are provided of the mating system from two wild hexaploid populations of the androdioecious European wind-pollinated plant M. annua with contrasting male frequencies. METHODS: Four diploid microsatellite loci were used to genotype 19-20 progeny arrays from two populations of M. annua, one with males and one without. Mating-system parameters were estimated using the program MLTR. KEY RESULTS: Both populations had similar, intermediate outcrossing rates (t(m) = 0·64 and 0·52 for the population with and without males, respectively). The population without males showed a lower level of correlated paternity and biparental inbreeding and higher allelic richness and gene diversity than the population with males. CONCLUSIONS: The results demonstrate the utility of new diploid microsatellite loci for mating system analysis in a hexaploid plant. It would appear that androdioecious M. annua has a mixed-mating system in the wild, an uncommon finding for wind-pollinated species. This study sets a foundation for future research to assess the relative importance of the sexual system, plant-density variation and stochastic processes for the regulation of male frequencies in M. annua over space and time.


Subject(s)
Diploidy , Euphorbiaceae/physiology , Euphorbiaceae/genetics , Genetic Variation , Genotype , Hermaphroditic Organisms , Microsatellite Repeats , Polyploidy , Reproduction/physiology
4.
Curr Biol ; 20(11): R482-4, 2010 Jun 08.
Article in English | MEDLINE | ID: mdl-20541495

ABSTRACT

Mating-system models have struggled to account for the high frequency of males found with hermaphrodites in a common Mediterranean shrub. The discovery of its unusual self-incompatibility system now provides an elegant and unexpected solution to the puzzle.


Subject(s)
Plant Physiological Phenomena , Pollination , Reproduction , Plants/anatomy & histology
5.
J Hered ; 101(4): 504-11, 2010.
Article in English | MEDLINE | ID: mdl-20219887

ABSTRACT

Mercurialis annua is a wind-pollinated annual showing a remarkable sexual-system variation, with hexaploid populations being either monoecious or androdioecious. Hexaploid M. annua is most likely a product of hybridization between diploid M. huetii and tetraploid M. annua; therefore, we developed microsatellite loci by isolating simple sequence repeat (SSR) sequences from the diploid progenitor, cross-amplification tests in M. huetii/M. annua species complex followed by selection of loci amplifying only in M. huetii and hexaploid M. annua, and testing polymorphism in 1 hexaploid population. This protocol resulted in 10 unlinked, polymorphic loci amplifying 4-10 alleles per locus. Due to specific amplification of the diploid part of the genome originating from M. huetii, these loci produce codominantly scored, diploid data for allohexaploid species, thereby simplifying data collection and subsequent analyses. Sequencing of the hexaploid polymerase chain reaction product for all 10 loci and aligning it with M. huetii SSR library sequence confirmed orthology of the characterized loci. Inheritance tests in 4 hexaploid crosses confirmed diploid Mendelian segregation of the new loci.


Subject(s)
Diploidy , Euphorbiaceae/genetics , Microsatellite Repeats/genetics , Chromosome Mapping , DNA, Plant/metabolism , Genetic Linkage , Genetic Loci , Genome, Plant , Minisatellite Repeats , Polymerase Chain Reaction , Sequence Analysis
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