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Hadaček, Franz
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Hadaček, Franz
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Hadaček, Franz
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Hadaček, F.
Hadacek, Franz
Hadacek, F.
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2013Journal Article [["dc.bibliographiccitation.firstpage","763"],["dc.bibliographiccitation.issue","11-12"],["dc.bibliographiccitation.journal","Journal of Phytopathology"],["dc.bibliographiccitation.lastpage","773"],["dc.bibliographiccitation.volume","161"],["dc.contributor.author","Hage-Ahmed, Karin"],["dc.contributor.author","Moyses, Anna"],["dc.contributor.author","Voglgruber, Andreas"],["dc.contributor.author","Hadacek, Franz"],["dc.contributor.author","Steinkellner, Siegrid"],["dc.date.accessioned","2018-11-07T09:16:46Z"],["dc.date.available","2018-11-07T09:16:46Z"],["dc.date.issued","2013"],["dc.description.abstract","Arbuscular mycorrhizal fungi (AMF) can control soilborne diseases such as Fusarium oxysporum f.sp. lycopersici (Fol). Root exudates play an important role in plant-microbe interactions in the rhizosphere, especially, in the initial phase of these interactions. In this work, we focus on (i) elucidating dynamics in root exudation of Solanum lycopersicum L. in an intercropping system due to AMF and/or Fol; (ii) its effect on Fol development in vitro; and (iii) the testing of the root exudate compounds identified in the chromatographic analyses in terms of effects on fungal growth in in vitro assays. GC-MS analyses revealed an AMF-dependent increase in sugars and decrease in organic acids, mainly glucose and malate. In the HPLC analyses, an increase in chlorogenic acid was evident in the combined treatment of AMF and Fol, which is to our knowledge the first report about an increase in chlorogenic acid in root exudates of AM plants challenged with Fol compared with plants inoculated with AMF only, clearly indicating changes in root exudation due to AMF and Fol. Root exudates of AMF tomato plants stimulate the germination rate of Fol, whereas the co-inoculation of AMF and Fol leads to a reduction in spore germination. In the in vitro assays, citrate and chlorogenic acid could be identified as possible candidates for the reduction in Fol germination rate in the root exudates of the AMF+Fol treatment because they proved inhibition at concentrations naturally occurring in the rhizosphere."],["dc.description.sponsorship","Austrian Science Fund (FWF) [P20923-B17]"],["dc.identifier.doi","10.1111/jph.12130"],["dc.identifier.isi","000330107700002"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28010"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.relation.issn","1439-0434"],["dc.relation.issn","0931-1785"],["dc.title","Alterations in Root Exudation of Intercropped Tomato Mediated by the Arbuscular Mycorrhizal Fungus Glomus mosseae and the Soilborne Pathogen Fusarium oxysporum f. sp lycopersici"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2015Journal Article [["dc.bibliographiccitation.firstpage","151"],["dc.bibliographiccitation.journal","Environmental and Experimental Botany"],["dc.bibliographiccitation.lastpage","160"],["dc.bibliographiccitation.volume","109"],["dc.contributor.author","Tewari, Rajesh Kumar"],["dc.contributor.author","Bachmann, Gert"],["dc.contributor.author","Hadacek, Franz"],["dc.date.accessioned","2018-11-07T10:04:18Z"],["dc.date.available","2018-11-07T10:04:18Z"],["dc.date.issued","2015"],["dc.description.abstract","The alkaloid 8-hydroxyquinoline (HQ) was pointed out as potential phytosiderophore that is taken up unspecifically by iron acquisition strategy I and II plants. HQ in root exudate of the knapweed Centaurea diffusa even was considered as a factor contributing to the invasive success of this species. This study compares the iron supply efficiencies of the Fe-HQ complex and Fe-EDTA in hydroponic cultures of rapeseed (Brassica napus) as a plant model system to explore the proposed function. Iron (FeCl3) was supplied in 2 and 10 mu M concentrations in a 1:1 ratio with the ligand (HQ). After 20 days, Fe content, lipid peroxidation, superoxide anion, hydrogen peroxide, and ascorbic acid concentrations, various enzyme activities associated with antioxidant defences and programmed cell death (PCD), and nuclear condensation were determined. Iron supply in the form of a Fe-HQ complex clearly was less efficient. These plants developed chlorosis and showed symptoms of non-autolytic PCD similar to those that had been subjected to Fe deprivation. Reactive oxygen species (ROS) concentration levels and enzyme activities (superoxide dismutase, catalase, alkaline protease, caspase-3-like and deoxyribonuclease) resembled more those observed in plants which suffered from Fe deprivation, than those of Fe-sufficient Fe-EDTA supplied plants. The results do not support the putative phytosiderophore function alleged to HQ in the studied concentration range (2-10 mu M) but instead corroborate the one hypothesis explaining HQ toxicity: Fe in complex with HQ is not released efficiently enough from the complex to be available for metalloenzymes that require it as a co-factor. (C) 2014 Elsevier B.V. All rights reserved."],["dc.identifier.doi","10.1016/j.envexpbot.2014.07.016"],["dc.identifier.isi","000345478000018"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/38665"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Pergamon-elsevier Science Ltd"],["dc.relation.issn","1873-7307"],["dc.relation.issn","0098-8472"],["dc.title","Iron in complex with the alleged phytosiderophore 8-hydroxyquinoline induces functional iron deficiency and non-autolytic programmed cell death in rapeseed plants"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI WOS2016Journal Article [["dc.bibliographiccitation.artnumber","278"],["dc.bibliographiccitation.journal","Frontiers in Plant Science"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Klatt, Simone"],["dc.contributor.author","Hadacek, Franz"],["dc.contributor.author","Brinkmann, Gina"],["dc.contributor.author","Eilerts, Marius"],["dc.contributor.author","Hojsgaard, Diego H."],["dc.contributor.author","Hodač, Ladislav"],["dc.contributor.author","Hörandl, Elvira"],["dc.date.accessioned","2018-11-07T10:16:55Z"],["dc.date.available","2018-11-07T10:16:55Z"],["dc.date.issued","2016"],["dc.description.abstract","Meiosis, the key step of sexual reproduction, persists in facultative apomictic plants functional to some extent. However, it still remains unclear how and why proportions of reproductive pathways vary under different environmental stress conditions. We hypothesized that oxidative stress mediates alterations of developmental pathways. In apomictic plants we expected that megasporogenesis, the stage directly after meiosis, would be more affected than later stages of seed development. To simulate moderate stress conditions we subjected clone-mates of facultative apomictic Ranunculus auricomus to 10 h photoperiods, reflecting natural conditions, and extended ones (16.5 h). Reproduction mode was screened directly after megasporogenesis (microscope) and at seed stage (flow cytometric seed screening). Targeted metabolite profiles were performed with HPLC-DAD to explore if and which metabolic reprogramming was caused by the extended photoperiod. Prolonged photoperiods resulted in increased frequencies of sexual vs. aposporous initials directly after meiosis, but did not affect frequencies of sexual vs. asexual seed formation. Changes in secondary metabolite profiles under extended photoperiods affected all classes of compounds, and c. 20% of these changes separated the two treatments. Unexpectedly, the renowned antioxidant phenylpropanoids and flavonoids added more to clone-mate variation than to treatment differentiation. Among others, chlorophyll degradation products, non-assigned phenolic compounds and more lipophilic metabolites also contributed to the dissimilarity of the metabolic profiles of plants that had been exposed to the two different photoperiods. The hypothesis of moderate light stress effects was supported by increased proportions of sexual megaspore development at the expense of aposporous initial formation. The lack of effects at the seed stage confirms the basic assumption that only meiosis and sporogenesis would be sensitive to light stress. The concomitant change of secondary metabolite profiles, as a systemic response at this early developmental stage, supports the notion that oxidative stress could have affected megasporogenesis by causing the observed metabolic reprogramming. Hypotheses of genotype-specific responses to prolonged photoperiods are rejected."],["dc.description.sponsorship","Open-Access Publikationsfonds 2016"],["dc.identifier.doi","10.3389/fpls.2016.00278"],["dc.identifier.isi","000371400600001"],["dc.identifier.pmid","27014302"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/12965"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/41132"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Frontiers Media S.A."],["dc.relation.eissn","1664-462X"],["dc.relation.issn","1664-462X"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Photoperiod Extension Enhances Sexual Megaspore Formation and Triggers Metabolic Reprogramming in Facultative Apomictic Ranunculus auricomus"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2019Journal Article [["dc.bibliographiccitation.artnumber","3044"],["dc.bibliographiccitation.issue","15"],["dc.bibliographiccitation.journal","Applied Sciences"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Kareem, Zana Jamal"],["dc.contributor.author","Su, Ling"],["dc.contributor.author","Rathgeb, Anna"],["dc.contributor.author","Sirrenberg, Anke"],["dc.contributor.author","Hadacek, Franz"],["dc.contributor.author","Rashid, Ahmad Hama Ameen H."],["dc.contributor.author","Karlovsky, Petr"],["dc.date.accessioned","2019-08-02T08:57:53Z"],["dc.date.available","2019-08-02T08:57:53Z"],["dc.date.issued","2019"],["dc.description.abstract","The volume and complexity of commercial bioreactors for sterile hydroponics and hairy roots are too large for comparative analysis of many cultures. Here a small-scale bioreactor fabricated from standard glass materials and suitable for both airlift and bubble aeration mode is described. The performance of the bioreactor was tested by growing oilseed rape (Brassica napus L.) and rose plants (Rosa canina L.) in sterile hydroponics and by cultivating hairy roots of henbane (Hyoscyamus niger L.) and sesame (Hyoscyamus niger L.). Plants grown in hydroponics for up to six weeks did not show chloroses or necroses. Hairy roots grew faster or comparably fast in bioreactors as compared to shaking flasks. Root exudates of roses and exudates of hairy roots of henbane were subjected to targeted and nontargeted analysis by HPLC coupled with optical and mass spectrometric detectors. The diversity and concentration of hairy root exudates were higher in bioreactors than in shaking flasks. The composition of hairy root exudates of three accessions of H. niger did not match the genetic relatedness among the accessions. Hairy roots of Hyoscyamus niger exuded salicylic acid in amounts varying among plant accessions and between bioreactors and shaking flask cultures."],["dc.identifier.doi","10.3390/app9153044"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16324"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/62265"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.relation.issn","2076-3417"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Small-Scale Bioreactor for Sterile Hydroponics and Hairy Roots: Metabolic Diversity and Salicylic Acid Exudation by Hairy Roots of Hyoscyamus niger"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI2014Journal Article [["dc.bibliographiccitation.firstpage","13"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Biology and Fertility of Soils"],["dc.bibliographiccitation.lastpage","23"],["dc.bibliographiccitation.volume","50"],["dc.contributor.author","Trouve, Raphael"],["dc.contributor.author","Drapela, Thomas"],["dc.contributor.author","Frank, Thomas"],["dc.contributor.author","Hadacek, Franz"],["dc.contributor.author","Zaller, Johann G."],["dc.date.accessioned","2018-11-07T09:47:03Z"],["dc.date.available","2018-11-07T09:47:03Z"],["dc.date.issued","2014"],["dc.description.abstract","Invasion of non-native species is among the top threats for the biodiversity and functioning of native and agricultural ecosystems worldwide. We investigated whether the herbivory of the slug Arion vulgaris (formerly Arion lusitanicus; Gastropoda), that is listed among the 100 worst alien species in Europe, is affected by soil organisms commonly present in terrestrial ecosystems (i.e. earthworms-Annelida: Lumbricidae and arbuscular mycorrhizal fungi-AMF, Glomerales). We hypothesized that slug herbivory would be affected by soil organisms via altered plant nutrient availability and plant quality. In a greenhouse experiment, we created a simple plant community consisting of a grass, a forb, and a legume species and inoculated these systems with either two earthworm species and/or four AMF taxa. Slugs were introduced after plants were established. Earthworms significantly reduced total slug herbivory in AMF-inoculated plant communities (P = 0.013). Across plant species, earthworms increased leaf total N and secondary metabolites, AMF decreased leaf thickness. Mycorrhizae induced a shift in slug feeding preference from non-legumes to legumes; the grass was generally avoided by slugs. AMF effects on legume herbivory can partly be explained by the AMF-induced increase in total N and decrease in C/N ratio; earthworm effects are less clear as no worm-induced alterations of legume plant chemistry were observed. The presence of earthworms increased average AMF colonization of plant roots by 140 % (P < 0.001). Total shoot mass was significantly increased by AMF (P < 0.001). These data suggest that the feeding behavior of this invasive slug is altered by a belowground control of plant chemical quality and community structure."],["dc.description.sponsorship","Austrian Science Fund (FWF project) [P20171-B16]"],["dc.identifier.doi","10.1007/s00374-013-0827-1"],["dc.identifier.isi","000329094600002"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10249"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/35020"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","1432-0789"],["dc.relation.issn","0178-2762"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Herbivory of an invasive slug in a model grassland community can be affected by earthworms and mycorrhizal fungi"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI WOS2015Conference Paper [["dc.bibliographiccitation.firstpage","103"],["dc.bibliographiccitation.journal","Journal of Organometallic Chemistry"],["dc.bibliographiccitation.lastpage","110"],["dc.bibliographiccitation.volume","782"],["dc.contributor.author","Chobot, Vladimir"],["dc.contributor.author","Hadacek, Franz"],["dc.contributor.author","Weckwerth, Wolfram"],["dc.contributor.author","Kubicova, Lenka"],["dc.date.accessioned","2018-11-07T09:58:30Z"],["dc.date.available","2018-11-07T09:58:30Z"],["dc.date.issued","2015"],["dc.description.abstract","Anthranilic acid (ANA) and 3-hydroxyanthranilic acid (3-HANA) are kynurenine pathway intermediates of the tryptophan metabolism. A hitherto unemployed method combination, differential pulse voltammetry, mass spectrometry (nano-ESI MS), deoxyribose degradation and iron(II) autoxidation assays has been employed for studying of their redox chemistry and their interactions with iron(II) and iron(III) ions. Both acids inhibited the Fenton reaction by iron chelation and ROS scavenging in the deoxyribose degradation assay. In the iron(II) autoxidation assay, anthranilic acid showed antioxidant effects, whereas 3-hydroxyanthranilic acid exhibited apparent pro-oxidant activity. The differential pulse voltammograms of free metabolites and their iron(II) coordination complexes reflected these properties. Nano-ESI MS confirmed ANA and 3-HANA as efficient iron(II) chelators, both of which form coordination complexes of ligand:iron(II) ratio 1:1, 2:1, and 3:1. In addition, nano-ESI MS analyses of the oxidation effects by hydroxyl radical attack identified 3-HANA as strikingly more susceptible than ANA. 3-HANA susceptibility to oxidation may explain its decreased concentrations in the reaction mixture. The presented observations can add to explaining why 3-HANA levels decrease in patients with some neurological and other diseases which can often associated with elevated concentrations of ROS. (C) 2015 The Authors. Published by Elsevier B.V."],["dc.description.sponsorship","Austrian Science Fund (FWF) [P24630-B21]"],["dc.identifier.doi","10.1016/j.jorganchem.2015.01.005"],["dc.identifier.isi","000351637900016"],["dc.identifier.pmid","25892823"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/37375"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Elsevier Science Sa"],["dc.publisher.place","Lausanne"],["dc.relation.conference","7th International Symposium on Bioorganometallic Chemistry"],["dc.relation.eventlocation","Vienna, AUSTRIA"],["dc.relation.issn","1872-8561"],["dc.relation.issn","0022-328X"],["dc.title","Iron chelation and redox chemistry of anthranilic acid and 3-hydroxyanthranilic acid: A comparison of two structurally related kynurenine pathway metabolites to obtain improved insights into their potential role in neurological disease development"],["dc.type","conference_paper"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2016Journal Article [["dc.bibliographiccitation.artnumber","41"],["dc.bibliographiccitation.journal","Parasite"],["dc.bibliographiccitation.volume","23"],["dc.contributor.author","Teichmann, Klaus"],["dc.contributor.author","Kuliberda, Maxime"],["dc.contributor.author","Schatzmayr, Gerd"],["dc.contributor.author","Pacher, Thomas"],["dc.contributor.author","Zitterl-Eglseer, Karin"],["dc.contributor.author","Joachim, Anja"],["dc.contributor.author","Hadacek, Franz"],["dc.date.accessioned","2018-11-07T10:08:32Z"],["dc.date.available","2018-11-07T10:08:32Z"],["dc.date.issued","2016"],["dc.description.abstract","Disposal of organic plant wastes and by-products from the food or pharmaceutical industries usually involves high costs. In the present study, 42 samples derived from such by-products were screened in vitro against Cryptosporidium parvum, a protozoan parasite that may contaminate drinking water and cause diarrhoea. The novel bioassay was previously established in the microtitre plate format. Human ileocaecal adenocarcinoma (HCT-8) cell cultures were seeded with C. parvum oocysts and parasite development was monitored by an indirect fluorescent antibody technique (IFAT) and microscopic assessment for clusters of secondary infection (CSI). Minimum inhibitory concentrations (MICs) and potential detrimental effects on the host cells were determined. An ethanolic extract from olive (Olea europaea) pomace, after oil pressing and phenol recovery, reproducibly inhibited C. parvum development (MIC = 250-500 mu g mL(-1), IC50 = 361 (279-438) mu g mL(-1), IC90 = 467 (398-615) mu g mL(-1)). Accordingly, tyrosol, hydroxytyrosol, trans-coniferyl alcohol and oleuropein were selected as reference test compounds, but their contributions to the observed activity of the olive pomace extract were insignificant. The established test system proved to be a fast and efficient assay for identifying anti-cryptosporidial activities in biological waste material and comparison with selected reference compounds."],["dc.identifier.doi","10.1051/parasite/2016050"],["dc.identifier.isi","000386254500001"],["dc.identifier.pmid","27627637"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/13978"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/39483"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Edp Sciences S A"],["dc.relation.issn","1776-1042"],["dc.relation.issn","1252-607X"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","In vitro inhibitory effects of plant-derived by-products against Cryptosporidium parvum"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2016Journal Article [["dc.bibliographiccitation.firstpage","531"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Heredity"],["dc.bibliographiccitation.lastpage","541"],["dc.bibliographiccitation.volume","116"],["dc.contributor.author","Gramlich, Susanne"],["dc.contributor.author","Sagmeister, P."],["dc.contributor.author","Dullinger, Stefan"],["dc.contributor.author","Hadacek, Franz"],["dc.contributor.author","Hoerandl, Elvira"],["dc.date.accessioned","2018-11-07T10:13:57Z"],["dc.date.available","2018-11-07T10:13:57Z"],["dc.date.issued","2016"],["dc.description.abstract","Little attention has been paid to the evolutionary consequences of the colonizing dynamics and succession processes following glacier retreat. Here we studied hybrid populations that have recently formed and established on glacier forefields of the European Alps owing to secondary contact of a lowland colonizer with a subalpine species. We analyzed the composition of two hybrid populations between Salix purpurea and Salix helvetica with nine microsatellite markers by using Bayesian methods (STRUCTURE and NewHybrids), and simulations. We also studied niche differentiation between the hybrids and the parental species based on indicator values, soil pH and water retention potential measurements. Allelic structure of hybrids confirms the assumed parentage and in situ origin of the crosses on two independent sites within the last decades. Both hybrid populations comprised F-1 and later generation hybrids (F-2 and backcrosses), confirming hybrid fertility. The parental species showed significant differences in niche characteristics for temperature, soil pH, nutrients and moisture. Remarkably, the hybrids exhibited a higher tolerance to cold temperatures, nutrient-poor and acidic soils than either parent. Our results show that willow hybrids originated after glacier retreat and have established persistent populations within a few decades. One factor contributing to hybrid establishment in sympatry with their parents is their ability to occupy more extreme niches than either parental species within a mosaic-like pattern of microhabitats on the forefield. Introgression and/or transgressive segregation may have resulted in novel genotypes that are able to expand the ecological spectrum of either parent."],["dc.identifier.doi","10.1038/hdy.2016.14"],["dc.identifier.isi","000375700100007"],["dc.identifier.pmid","26980342"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/13482"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/40526"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Nature Publishing Group"],["dc.relation.issn","1365-2540"],["dc.relation.issn","0018-067X"],["dc.rights","CC BY-NC-SA 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by-nc-sa/4.0"],["dc.title","Evolution in situ: hybrid origin and establishment of willows (Salix L.) on alpine glacier forefields"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2019Journal Article [["dc.bibliographiccitation.firstpage","476"],["dc.bibliographiccitation.issue","10"],["dc.bibliographiccitation.journal","Antioxidants"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Kubicova, Lenka"],["dc.contributor.author","Hadacek, Franz"],["dc.contributor.author","Bachmann, Gert"],["dc.contributor.author","Weckwerth, Wolfram"],["dc.contributor.author","Chobot, Vladimir"],["dc.date.accessioned","2020-12-10T18:46:56Z"],["dc.date.available","2020-12-10T18:46:56Z"],["dc.date.issued","2019"],["dc.description.sponsorship","Austrian Science Fund"],["dc.identifier.doi","10.3390/antiox8100476"],["dc.identifier.eissn","2076-3921"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17062"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/78593"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.publisher","MDPI"],["dc.relation.eissn","2076-3921"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Coordination Complex Formation and Redox Properties of Kynurenic and Xanthurenic Acid Can Affect Brain Tissue Homeodynamics"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]Details DOI2020Journal Article [["dc.bibliographiccitation.firstpage","1"],["dc.bibliographiccitation.issue","1-2"],["dc.bibliographiccitation.journal","Heredity"],["dc.bibliographiccitation.lastpage","14"],["dc.bibliographiccitation.volume","125"],["dc.contributor.author","Hörandl, Elvira"],["dc.contributor.author","Hadacek, Franz"],["dc.date.accessioned","2020-12-10T18:09:44Z"],["dc.date.available","2020-12-10T18:09:44Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1038/s41437-020-0317-9"],["dc.identifier.eissn","1365-2540"],["dc.identifier.issn","0018-067X"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/73741"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Oxygen, life forms, and the evolution of sexes in multicellular eukaryotes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]Details DOI
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