Oleksandra Kuchma

Dr. Oleksandra Kuchma

Department of Forest Genetics and Forest Tree Breeding, University of Göttingen
orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2018 in Global Ecology and Conservation
Verified
Journal Article
Open access
CLCorsa Lok Ching Liu
Corsa Lok Ching Liu
Oleksandra KuchmaOleksandra Kuchma
Oleksandra Kuchma
Konstantin KrutovskyKonstantin Krutovsky
Konstantin Krutovsky

18 July 2011 in Mutation Research - Genetic Toxicology and Environmental Mutagenesis
Verified
Journal Article
Closed access
Oleksandra KuchmaOleksandra Kuchma
Oleksandra Kuchma
BVBarbara Vornam
Barbara Vornam
RFReiner Finkeldey
Reiner Finkeldey

27 November 2012 in Plant Systematics and Evolution
Verified
Journal Article
Open access
PDF file
LLLudger Leinemann
Ludger Leinemann
WSWilfried Steiner
Wilfried Steiner
BHBernhard Hosius
Bernhard Hosius
Oleksandra KuchmaOleksandra Kuchma
Oleksandra Kuchma
WAWolfgang Arenhövel
Wolfgang Arenhövel
RFReiner Finkeldey
Reiner Finkeldey
Corylus avellana L. (hazel) is a long-lived, monoecious and wind-pollinated shrub species, widespread all over Europe. In Germany, hazel is intensively traded and planted, and thus is of central interest from a nature conservancy point of view. To assess the within- and between-population differentiation of hazel, 20 natural populations (18 from Germany, one from Italy and one from Hungary) were investigated genetically. Seven isozyme systems comprising 11 gene loci were analysed in up to 100 samples (average 92.6) per population, amplified fragment length polymorphisms (AFLP) were analysed in up to 50 samples (average 47.4) and nine cpDNA-SSR markers were assessed in 20 samples per population. Results for overall isozyme variability with Na 2.46 alleles per locus, allelic diversity (Ne) 1.39, expected heterozygosity He 21 % and 79 % polymorphic loci were in accordance with the findings of previous studies. The respective values for AFLPs were lower, but both marker systems revealed the same level of about 3.5 % differentiation between populations. For cpSSR only the Italian sample showed within-population variation and the two haplotypes were completely differentiated from all other populations expressing a unique genetic structure with one single haplotype. Among the three marker systems AFLPs showed the best ability to differentiate between populations. While only one isozyme locus revealed significant differentiation, 41 AFLP loci showed highly significant differentiation between all populations, but 26 loci when only German populations were considered. Consequently geographic differentiation analyses focused mainly on molecular markers. Mantel tests showed significant correlations between genetic and geographic distance, but in the unweighted pair-group method with arithmetic mean analyses, adjacent populations did not always form clusters. While chloroplast markers were able to clearly distinguish only the Hungarian population, the nuclear markers revealed clear spatial genetic structures. The correlations between geographic and genetic distance was high for AFLPs. The correlograms illustrate this effect for all populations as well as for the German populations.

1 June 2011 in Environmental Pollution
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Journal Article
Closed access
Oleksandra KuchmaOleksandra Kuchma
Oleksandra Kuchma
RFReiner Finkeldey
Reiner Finkeldey

27 March 2014 in Plant Systematics and Evolution
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Journal Article
Closed access
PDF file
LLLudger Leinemann
Ludger Leinemann
JKJörg Kleinschmit
Jörg Kleinschmit
BFBarbara Fussi
Barbara Fussi
BHBernhard Hosius
Bernhard Hosius
Oleksandra KuchmaOleksandra Kuchma
Oleksandra Kuchma
RFReiner Finkeldey
Reiner Finkeldey

11 February 2024 in Conservation Genetics
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Journal Article
Open access
PDF file
HLHeike Liesebach
Heike Liesebach
PEPascal Eusemann
Pascal Eusemann
AHAki M. Höltken
Aki M. Höltken
UTUte Tröber
Ute Tröber
Oleksandra KuchmaOleksandra Kuchma
Oleksandra Kuchma
BFBarbara Fussi
Barbara Fussi
Genetic diversity is considered to be a prerequisite for adaptation and adaptability as it is a key element of biological diversity. However, the monitoring of genetic diversity has tended to be ignored in biodiversity monitoring. We report a comprehensive genetic monitoring effort in two dominant forest tree species, which was started with a baseline survey in 12 European beech populations and 10 Norway spruce populations in Germany. The standardized experimental design is based on collecting samples of at least 250 adult trees, and 400 natural regeneration and 400 seed samples and their genotyping with 15–16 high-resolution SSR markers. In addition to commonly used mean values across the markers to quantify genetic diversity, we placed special emphasis on various marker-based, pedigree-based and demographic models for estimating the contemporary effective population size Ne of the different generations. In both beech and spruce, no variation in genetic diversity with mean values across markers was detectable between the studied stands and between age cohorts. We detected that stable allelic diversity in progeny generations is ensured by sufficient gene flow from surrounding forests. However, estimates of effective population size show marked differentiation among populations and among age cohorts. Natural regeneration samples appear to converge on the parent generation, while seed samples show a clear bottleneck effect. The Ne parameter can be used to derive conclusions for sustainable natural regeneration management in forest stands and for seed stand approvals including adequate seed collections for appropriate artificial regenerations.The sibship frequency-based method for Ne estimates is presented as much more robust than the widely used LD estimates, which often fail for samples with too weak relatedness. Despite the distinct kinship structure in our monitoring plots, the contemporary effective population size proves to be an essential parameter for assessing the integrity of the reproductive system.