Finkeldey, Reiner

[["dc.bibliographiccitation.firstpage","116"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Plant Biology"],["dc.bibliographiccitation.lastpage","126"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Curtu, Alexandru Lucian"],["dc.contributor.author","Gailing, Oliver"],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Finkeldey, Reiner"],["dc.date.accessioned","2018-11-07T11:07:27Z"],["dc.date.accessioned","2020-05-13T12:20:00Z"],["dc.date.available","2018-11-07T11:07:27Z"],["dc.date.available","2020-05-13T12:20:00Z"],["dc.date.issued","2007"],["dc.description.abstract","Chloroplast DNA and two categories of nuclear markers - isozymes and microsatellites - were used to examine a very rich natural community of oaks (Quercus spp.) situated in west-central Romania. The community consists of five oak species: Q. robur, Q. petraea, Q. pubescens, and Q. frainetto - that are closely related -, and Q. cerris. A total of five chloroplast haplotypes was identified. Q. cerris was fixed for a single haplotype. The other four species shared the two most common haplotypes. One haplotype was confined to Q. robur and a very rare one was restricted to Q. petraea. Both types of nuclear markers revealed a larger genetic variation for Q. pubescens and Q. petraea than for Q. frainetto and Q. robur, although the differences between species are in most cases not significant. At the nuclear level, Q. cerris could be clearly separated from the other four oak species confirming the taxonomic classification. Regardless of the estimate used, the levels of polymorphism revealed by microsatellites were much higher than those based on isozymes. For the four closely related species the overall genetic differentiation was significant at both categories of nuclear markers. Several loci, such as Acp-C for isozymes, and ssrQpZAG36 and ssrQrZAG96 for microsatellites were very useful to discriminate among species. However, the level of differentiation varied markedly between pairs of species. The genetic affinities among the species may reflect different phylogenetic distances and/or different rates of recurrent gene flow at this site."],["dc.identifier.doi","10.1055/s-2006-924542"],["dc.identifier.isi","000243988100014"],["dc.identifier.pmid","17048143"],["dc.identifier.scopus","2-s2.0-33846856208"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/52565"],["dc.identifier.url","http://www.scopus.com/inward/record.url?eid=2-s2.0-33846856208&partnerID=MN8TOARS"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","1435-8603"],["dc.title","Genetic variation and differentiation within a natural community of five oak species (Quercus spp.)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","45"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Plant Molecular Biology Reporter"],["dc.bibliographiccitation.lastpage","55"],["dc.bibliographiccitation.volume","24"],["dc.contributor.author","Rachmayanti, Yanti"],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Gailing, Oliver"],["dc.contributor.author","Finkeldey, Reiner"],["dc.date.accessioned","2018-11-07T10:15:56Z"],["dc.date.accessioned","2020-05-13T12:15:39Z"],["dc.date.available","2018-11-07T10:15:56Z"],["dc.date.available","2020-05-13T12:15:39Z"],["dc.date.issued","2006"],["dc.description.abstract","A successful DNA extraction from wood yielding appropriate DNA quality for PCR amplification allows molecular genetic investigations of wood tissue. Genotypes, the origin of sampled material, and species can be identified based on an investigation of wood if suitable information on genetic variation patterns within and among species is available. Potential applications are in forensics and in the control of the timber and wood trade. We extracted DNA from wood of Dipterocarpaceae, a family that dominates rainforests and comprises many important timber species in Southeast Asia. Several different DNA isolation techniques were compared and optimized for wood samples from natural populations and from wood processing enterprises. The quality of the DNA was tested by spectrophotometry, PCR amplification, and PCR inhibitor tests. An average DNA yield of 2.2 mu g was obtained per 50-100 mg of dried wood sample. Chloroplast DNA (cpDNA) regions of different length were amenable to PCR amplification from the extracted DNA. Modification of DNA isolation techniques by the addition of polyvinylpyrrolidone (PVP) addition up to 3.1% into lysis buffer reduced PCR inhibition effectively. In order to evaluate the extraction method, we analyzed leaves and wood from the same tree by PCR amplification, genotyping and sequencing of chloroplast microsatellites."],["dc.identifier.doi","10.1007/BF02914045"],["dc.identifier.isi","000241601400004"],["dc.identifier.scopus","2-s2.0-33749539124"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65335"],["dc.identifier.url","http://www.scopus.com/inward/record.url?eid=2-s2.0-33749539124&partnerID=MN8TOARS"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.eissn","1572-9818"],["dc.relation.issn","0735-9640"],["dc.title","Extraction, amplification and characterization of wood DNA from Dipterocarpaceae"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Tree Genetics & Genomes"],["dc.bibliographiccitation.volume","14"],["dc.contributor.author","Eliades, Nicolas-George Homer"],["dc.contributor.author","Fady, B."],["dc.contributor.author","Gailing, Oliver"],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Finkeldey, Reiner"],["dc.date.accessioned","2020-05-13T12:33:37Z"],["dc.date.available","2020-05-13T12:33:37Z"],["dc.date.issued","2018"],["dc.description.abstract","Cedrus brevifolia is a narrowly distributed conifer species, currently limited to a single mountain in Cyprus, growing in restricted habitats on sites of different densities and sizes. This study assessed the influence of seed and pollen dispersal, as well as the effect of demographic and genetic features on the magnitude of fine-scale spatial genetic structure (SGS). Sampling was performed in 11 plots where 50 neighboring adult trees were sampled from each plot, while biparentally and paternally inherited genomes were used for analysis with microsatellites. Fine-scale SGS was significant but showed contrasting patterns among plots. Although the magnitude of SGS in C. brevifolia mainly results from restricted seed dispersal, short-distance pollen dispersal could also explain fine-scale SGS in some plots, which is rather uncommon in wind-pollinated conifer species. The lack of a general and consistent trend of SGS among plots and between genomes indicates that pollen and seed dispersal varies at plot level. The complex SGS patterns in C. brevifolia may result from the unequal ratio of male and female strobilies of trees within the same plots, at different reproductive periods. Demographic features such as habitat fragmentation did not influence the magnitude of SGS in C. brevifolia, whereas low tree aggregation reduced it. Further, the significant correlation observed between linkage disequilibrium (LD) and plots with significant SGS supports the assumption that under specific conditions, LD is likely to be caused by the magnitude of SGS."],["dc.identifier.doi","10.1007/s11295-018-1231-7"],["dc.identifier.scopus","2-s2.0-85041291252"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65359"],["dc.identifier.url","http://www.scopus.com/inward/record.url?eid=2-s2.0-85041291252&partnerID=MN8TOARS"],["dc.language.iso","en"],["dc.relation.eissn","1614-2950"],["dc.relation.issn","1614-2942"],["dc.title","Significant patterns of fine-scale spatial genetic structure in a narrow endemic wind-dispersed tree species, Cedrus brevifolia Henry"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","21"],["dc.bibliographiccitation.issue","1-2"],["dc.bibliographiccitation.journal","ALLGEMEINE FORST UND JAGDZEITUNG"],["dc.bibliographiccitation.lastpage","28"],["dc.bibliographiccitation.volume","175"],["dc.contributor.author","Cao, C. P."],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Ziehe, Martin"],["dc.contributor.author","Finkeldey, Reiner"],["dc.date.accessioned","2018-11-07T10:51:53Z"],["dc.date.available","2018-11-07T10:51:53Z"],["dc.date.issued","2004"],["dc.description.abstract","Yew (Taxus baccata L.) is a rare dioecious tree species in Europe. The object of this study is to characterize the genetic variation within and between 6 yew stands using isozyme and cpDNA (PCR-RFLPs and cpSSRs) markers. This study should enlarge the basis for the conservation measures of genetic resources of yew. Genotyping of individual trees has been carried out by analysis of bud material. For isozyme analysis, 6 isozyme genloci with altogether 19 alleles were investigated (Table 2). Results of data analysis revealed a high level of genetic variation within the investgated populations with a mean number of alleles per locus (A/L) of 2.6, a diversity (upsilon) of 1.48, an expected beterozygosity (H-e) of 31.6% and an observed heterozygosity (H-o) of 34.0%. The largest variation (1.6 less than or equal to upsilon less than or equal to 1.7, 36.4% less than or equal to H-e less than or equal to 41.4%) was found in the populations Hedemundener Gerneindewald (HM), Burgberg Thurnhosbach (TH) and Lohkopf (LK). The stands Naturwaldzelle Eichenberg (NZ, Abt. 249) and Naturwaldzelle Eichenberg (NWZ, Abt. 250) were genetically the least variable (1.2 less than or equal to upsilon less than or equal to 1.3, 19.6% less than or equal to H-c less than or equal to 24.2%) (Table 3). Comparisons between the genetic structures of male and female trees within stands indicated remarkable differences which were probably caused by genetic drift (Table 4). Variation between populations was measured using genetic distance d(o) and genetic differentiation D-j. The stands Burgberg Thurnhosbach (TH) and Lohkopf (LK) differed from the others substantially both in genetic distance (Table 5, Figure 1) and in genetic differentiation (Figure 3) concerning genetic structures. The mean differentiation 6 between stands amounted to 19.5% (Figure 3). Over all observed gene loci, the genetic structures of those stands which are located in the same geographical areas showed the smallest differences (Figure 1). Regarding the relatively high genetic variation within and the high differentiation between yew stands, it appears necessary to plan conservation measures on a broad basis of stands. The analysis of genetic variation within and between populations of yew was completed by cpDNA analysis at 5 trees per stand, respectively. As compared with other conifers like Abies alba and Picea abies with considerable variability, no cp-DNA variation has been observed for Taxus baccata L. in this study."],["dc.identifier.isi","000220166000004"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/48991"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","J D Sauerlanders Verlag"],["dc.relation.issn","0002-5852"],["dc.title","Study of genetic variation and differentiation of yew (Taxus baccata L.) stands using isozyme and DNA marker."],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","11"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","New Phytologist"],["dc.bibliographiccitation.lastpage","20"],["dc.bibliographiccitation.volume","170"],["dc.contributor.author","Dučić, Tanja"],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Finkeldey, Reiner"],["dc.contributor.author","Polle, Andrea"],["dc.date.accessioned","2017-09-07T11:49:17Z"],["dc.date.available","2017-09-07T11:49:17Z"],["dc.date.issued","2006"],["dc.description.abstract","Summary - Douglas fir (Pseudotsuga menziesii) variety glauca (DFG) but not the variety viridis (DFV) showed symptoms of manganese (Mn) toxicity in some field sites. We hypothesized that these two varieties differed in Mn metabolism. - To test this hypothesis, biomass partitioning, Mn concentrations, subcellular localization and 54Mn‐transport were investigated. - Total Mn uptake was three‐times higher in DFG than in DFV. DFV retained > 90% of 54Mn in roots, whereas > 60% was transported to the shoot in DFG. The epidermis was probably the most efficient Mn barrier since DFV contained lower Mn concentrations in cortical cells and vacuoles of roots than DFG. In both varieties, xylem loading was restricted and phloem transport was low. However, sieve cells still contained high Mn concentrations. - DFV displayed higher biomass production and higher shoot : root ratios than DFG. Our results clearly show that both varieties of Douglas fir differ significantly in Mn‐uptake and allocation patterns rendering DFG more vulnerable to Mn toxicity."],["dc.identifier.doi","10.1111/j.1469-8137.2006.01666.x"],["dc.identifier.gro","3147233"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/4864"],["dc.language.iso","en"],["dc.notes.status","final"],["dc.notes.submitter","chake"],["dc.relation.issn","0028-646X"],["dc.title","Uptake and translocation of manganese in seedlings of two varieties of Douglas fir (Pseudotsuga menziesii var. viridis and glauca)"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dc.type.peerReviewed","no"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2115"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Plant Systematics and Evolution"],["dc.bibliographiccitation.lastpage","2125"],["dc.bibliographiccitation.volume","300"],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Kleinschmit, Joerg"],["dc.contributor.author","Fussi, Barbara"],["dc.contributor.author","Hosius, Bernhard"],["dc.contributor.author","Kuchma, Oleksandra"],["dc.contributor.author","Arenhoevel, Wolfgang"],["dc.contributor.author","Lemmen, Patrick"],["dc.contributor.author","Kaetzel, Ralf"],["dc.contributor.author","Rogge, Martin"],["dc.contributor.author","Finkeldey, Reiner"],["dc.date.accessioned","2018-11-07T09:33:11Z"],["dc.date.available","2018-11-07T09:33:11Z"],["dc.date.issued","2014"],["dc.description.abstract","Sloe (Prunus spinosa L.) is a shrub native to Europe. In Germany, 50-80 % of all planted sloe is imported. Little is known about the genetic diversity patterns within and between German sloe populations. Thus, a debate arose how to avoid risks for nature and landscape by planting potentially maladapted material. The main objectives of our study are to analyse the genetic differentiation pattern of sloe populations in Germany, to identify geographic/genetic structures and to evaluate their potential for tracing reproductive material. 17 natural populations from Germany and 1 from Italy and Hungary were investigated by Amplified Fragment Length Polymorphisms (AFLP) and PCR-RFLP techniques. The AMOVA analyses based on AFLPs for all populations and for the German populations only result in equally high differentiation values of I broken vertical bar(PT) = 15 % of molecular variance between populations. The analysis of cpDNA PCR-RFLPs resulted in 24 haplotypes with 30 % showing genetic variation between populations. Overall values of genetic variability over all loci and populations are: Na = 0.832, Ne = 1.114 and He = 0.072. Mantel tests for AFLPs and cpDNA haplotypes reveal no association between geographic and genetic distances between populations as a result of a lack of differentiation between German populations and those from southern and southeastern Europe. Weak geographic/genetic patterns were observed on a large scale. However, these concern the German populations only. Our results indicate that vegetative regeneration in combination with founder effects may influence the level of differentiation between populations. Populations with a large amount of vegetative propagation are more differentiated from other populations than those populations which exhibit less vegetative regeneration. The assignment of reproductive material (i.e. plant material) to potential source populations resulted in high values of correct allocations. Hence, such methods can be applied to trace reproductive material of unknown origin."],["dc.identifier.doi","10.1007/s00606-014-1027-7"],["dc.identifier.isi","000344175100015"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/31911"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.publisher.place","Wien"],["dc.relation.issn","1615-6110"],["dc.relation.issn","0378-2697"],["dc.title","Genetic composition and differentiation of sloe (Prunus spinosa L.) populations in Germany with respect to the tracing of reproductive plant material"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Allgemeine Forst- und Jagdzeitung"],["dc.bibliographiccitation.volume","174"],["dc.contributor.author","Gailing, Oliver"],["dc.contributor.author","Wachter, H."],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Hosius, B."],["dc.contributor.author","Finkeldey, Reiner"],["dc.contributor.author","Schmitt, H.-P"],["dc.contributor.author","Heyder, J."],["dc.date.accessioned","2020-05-13T10:48:07Z"],["dc.date.available","2020-05-13T10:48:07Z"],["dc.date.issued","2003"],["dc.identifier.scopus","2-s2.0-0346038989"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65289"],["dc.identifier.url","http://www.scopus.com/inward/record.url?eid=2-s2.0-0346038989&partnerID=MN8TOARS"],["dc.language.iso","en"],["dc.title","Characterisation of different provenances of late flushing pedunculate oak (Quercus robur L.) with chloroplast markers,Charakterisierung verschiedener Ursprungsgebiete der Späteiche (Quercus robur L.) mit Hilfe von DNS-Markern aus dem Chloroplastengenom"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","509"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Physiologia Plantarum"],["dc.bibliographiccitation.lastpage","519"],["dc.bibliographiccitation.volume","137"],["dc.contributor.author","Gailing, Oliver"],["dc.contributor.author","Vornam, Barbara"],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Finkeldey, Reiner"],["dc.date.accessioned","2018-11-07T11:21:44Z"],["dc.date.accessioned","2020-05-13T11:59:13Z"],["dc.date.available","2018-11-07T11:21:44Z"],["dc.date.available","2020-05-13T11:59:13Z"],["dc.date.issued","2009"],["dc.description.abstract","With the increasing availability of sequence information at putatively important genes or regulatory regions, the characterization of adaptive genetic diversity and their association with phenotypic trait variation becomes feasible for many non-model organisms such as forest trees. Especially in predominantly outcrossing forest tree populations with large effective size, a high genetic variation in relevant genes is maintained, that is the raw material for the adaptation to changing and variable environments, and likewise for plant breeding. Oaks (Quercus spp.) are excellent model species to study the adaptation of forest trees to changing environments. They show a wide geographic distribution in Europe as dominant tree species in many forests and grow under a wide range of climatic and edaphic conditions. With the availability of a growing amount of functional and expressional candidate genes, we are now able to test the functional importance of single nucleotide polymorphisms (SNPs) by associating nucleotide variation in these genes with phenotypic variation in adaptive traits in segregating or natural populations. Here, we report on quantitative trait locus (QTL), candidate gene and association mapping approaches that are applicable to characterize gene markers and SNPs associated with variation in adaptive traits, such as bud burst, drought resistance and other traits showing selective responses to environmental change and stress. Because genome-wide association mapping studies are not feasible because of the enormous amount of SNP markers required in outcrossing trees with high recombination rates, the success of such an approach depends largely on the reasonable selection of candidate genes."],["dc.identifier.doi","10.1111/j.1399-3054.2009.01263.x"],["dc.identifier.isi","000271975700020"],["dc.identifier.pmid","19627554"],["dc.identifier.scopus","2-s2.0-70450265626"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/55849"],["dc.identifier.url","http://www.scopus.com/inward/record.url?eid=2-s2.0-70450265626&partnerID=MN8TOARS"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","0031-9317"],["dc.title","Genetic and genomic approaches to assess adaptive genetic variation in plants: Forest trees as a model"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","185"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Forensic Science International Genetics"],["dc.bibliographiccitation.lastpage","192"],["dc.bibliographiccitation.volume","3"],["dc.contributor.author","Rachmayanti, Yanti"],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Gailing, Oliver"],["dc.contributor.author","Finkeldey, Reiner"],["dc.date.accessioned","2018-11-07T08:29:09Z"],["dc.date.accessioned","2020-05-14T07:37:30Z"],["dc.date.available","2018-11-07T08:29:09Z"],["dc.date.available","2020-05-14T07:37:30Z"],["dc.date.issued","2009"],["dc.description.abstract","Molecular genetic markers have numerous potential applications in environmental forensics if DNA can be isolated from 'difficult' non-human biological material such as hairs, feathers, or wood. The identification of the origin of wood is particularly important in order to identify illegally harvested and traded timber and wood products. We describe success rates of DNA isolation from wood based on a simple, previously published extraction protocol. The protocol was used to isolate DNA from a total of 406 wood samples, mainly of the important tropical tree family Dipterocarpaceae. The reliability of the extraction method was confirmed by comparing fragment sizes and sequences after isolation of DNA from leaves and wood of the same trees. We observed the success of amplification of chloroplast DNA (cpDNA) fragments of different lengths by means of PCR, investigated key factors influencing PCR, and conducted inhibitor tests for a subset of the samples. The average rate of successful PCR amplification was 75.7%. Main factors influencing the success of PCR amplification were the size of the amplified fragment and the processing Status of the wood. Short fragments and unprocessed wood resulted in higher success rates. The success rate was also dependent on the age (storage duration) of the wood probe and on the investigated species. Amplification success was higher if DNA was isolated from outer sapwood (without cambium) in comparison to DNA isolated from the transition zone between sapwood and heartwood and the inner heartwood. However, inhibitor tests also indicated more PCR inhibitory substances in the outer sapwood in comparison to transition wood and heartwood. The addition of polyvinyl pyrolidone (PVP) to the lysis buffer proved to be highly efficient to improve the amplification success if inhibitory substances were present. (C) 2009 Elsevier Ireland Ltd. All rights reserved."],["dc.identifier.doi","10.1016/j.fsigen.2009.01.002"],["dc.identifier.isi","000266805700007"],["dc.identifier.pmid","19414167"],["dc.identifier.scopus","2-s2.0-67349101863"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65402"],["dc.identifier.url","http://www.scopus.com/inward/record.url?eid=2-s2.0-67349101863&partnerID=MN8TOARS"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","1872-4973"],["dc.title","DNA from processed and unprocessed wood: Factors influencing the isolation success"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","275"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","European Journal of Forest Research"],["dc.bibliographiccitation.lastpage","285"],["dc.bibliographiccitation.volume","138"],["dc.contributor.author","Pettenkofer, T."],["dc.contributor.author","Burkardt, K."],["dc.contributor.author","Ammer, Christian"],["dc.contributor.author","Vor, T."],["dc.contributor.author","Finkeldey, Reiner"],["dc.contributor.author","Müller, Markus"],["dc.contributor.author","Krutovsky, Konstantin V."],["dc.contributor.author","Vornam, B."],["dc.contributor.author","Leinemann, Ludger"],["dc.contributor.author","Gailing, Oliver"],["dc.date.accessioned","2020-05-12T14:53:08Z"],["dc.date.available","2020-05-12T14:53:08Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1007/s10342-019-01167-5"],["dc.identifier.scopus","2-s2.0-85061258706"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65259"],["dc.identifier.url","http://www.scopus.com/inward/record.url?eid=2-s2.0-85061258706&partnerID=MN8TOARS"],["dc.language.iso","en"],["dc.relation.eissn","1612-4677"],["dc.relation.issn","1612-4669"],["dc.relation.orgunit","Abteilung Forstgenetik und Forstpflanzenzüchtung"],["dc.title","Genetic diversity and differentiation of introduced red oak (Quercus rubra) in Germany in comparison with reference native North American populations"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]