Friedl, Thomas

[["dc.bibliographiccitation.firstpage","355"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","FEMS Microbiology Ecology"],["dc.bibliographiccitation.lastpage","372"],["dc.bibliographiccitation.volume","84"],["dc.contributor.author","Hallmann, Christine"],["dc.contributor.author","Stannek, Lorena"],["dc.contributor.author","Fritzlar, Diana"],["dc.contributor.author","Hause-Reitner, Dorothea"],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Hoppert, Michael"],["dc.date.accessioned","2018-11-07T09:25:36Z"],["dc.date.available","2018-11-07T09:25:36Z"],["dc.date.issued","2013"],["dc.description.abstract","Composition and diversity of aeroterrestrial phototrophic microbial communities are up to now poorly understood. Here, we present a comparative study addressing the composition of algal communities on sandstone substrata based upon the analysis of rRNA gene clone libraries from environmental samples and crude cultures. From a west-facing, shaded wall area of the mediaeval castle ruin Gleichen (Thuringia, Germany), sequences mainly related to the green algae Prasiococcus and Trebouxia (Trebouxiophyceae) were retrieved. A south-west-facing, sun-exposed wall area was mainly colonized by Apatococcus and a Phyllosiphon-related alga. Just a few species, in particular Stichococcus-related strains, were ubiquitous in both areas. Samples from a basement vault exposed to low irradiance exhibited Chlorophyceae like Chromochloris and Bracteacoccus. Thus, most green algae on the daylight-exposed walls were affiliated to Trebouxiophyceae, whereas Chlorophyceae were dominant in samples taken from the site kept under low irradiance. Accordingly, cyanobacterial communities were different: the sun-exposed area was dominated by Synechococcus-related organisms, while on the shaded wall area, cyanobacteria were almost absent. The filamentous Leptolyngbya dominated samples from the basement vault. Scanning electron microscopy revealed endolithic algal morphotypes (coccoid algae and diatoms) dominant in open pores between mineral particles. Here, the organisms may be also involved in biogenic weathering of stone."],["dc.identifier.doi","10.1111/1574-6941.12065"],["dc.identifier.isi","000317430200012"],["dc.identifier.pmid","23278436"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/30101"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-blackwell"],["dc.relation.issn","0168-6496"],["dc.title","Molecular diversity of phototrophic biofilms on building stone"],["dc.type","review"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Phycologia"],["dc.bibliographiccitation.volume","44"],["dc.contributor.author","Rindi, Fabio"],["dc.contributor.author","Sherwood, Alison R."],["dc.contributor.author","McIvor, Lynne"],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Guiry, Michael D."],["dc.contributor.author","Sheath, Robert G."],["dc.date.accessioned","2018-11-07T09:34:52Z"],["dc.date.available","2018-11-07T09:34:52Z"],["dc.date.issued","2005"],["dc.format.extent","86"],["dc.identifier.isi","000205501500206"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/32268"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Int Phycological Soc"],["dc.publisher.place","Lawrence"],["dc.relation.issn","0031-8884"],["dc.title","GENUS AND SPECIES-LEVEL PHYLOGENY IN THE PRASIOLALES (TREBOUXIOPHYCEAE, CHLOROPHYTA)"],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","359"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","CRYOLETTERS"],["dc.bibliographiccitation.lastpage","376"],["dc.bibliographiccitation.volume","28"],["dc.contributor.author","Day, John G."],["dc.contributor.author","Lorenz, Maike"],["dc.contributor.author","Wilding, Thomas A."],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Harding, Keith"],["dc.contributor.author","Prochold, Thomas"],["dc.contributor.author","Brennan, Debra"],["dc.contributor.author","Mueller, Julia"],["dc.contributor.author","Santos, Lilia M. A."],["dc.contributor.author","Santos, M. Fatima"],["dc.contributor.author","Osorio, Hugo C."],["dc.contributor.author","Amaral, Raquel"],["dc.contributor.author","Lukesova, Alena"],["dc.contributor.author","Hrouzek, Pavel"],["dc.contributor.author","Lukes, Martin"],["dc.contributor.author","Elster, Josef"],["dc.contributor.author","Lukavsky, Jaromir"],["dc.contributor.author","Probert, Ian"],["dc.contributor.author","Ryan, Matthew J."],["dc.contributor.author","Benson, Erica E."],["dc.date.accessioned","2018-11-07T10:58:50Z"],["dc.date.available","2018-11-07T10:58:50Z"],["dc.date.issued","2007"],["dc.description.abstract","Two cryopreservation methods, colligative cryoprotection coupled with controlled cooling and vitrification-based, encapsulation-dehydration were validated by five members of the EU Research Infrastructure consortium, COBRA, and two independent external validators. The test strain Chlorella vulgaris SAG 211-11b was successfully cryopreserved using two-step cooling employing passive (Mr Frosty((R))) and Controlled Rate Freezers (CRF) attaining the desired recovery target within 15% of the median viability level (94%). Significant differences (P<0.05) between cooling regimes were observed where Mr Frosty((R)) was more variable (Inter-Quartile Range being 21.5%, versus 13.0% for CRF samples). Viability assessment using fluorescein diacetate gave significantly (P<0.0001) higher survival than growth in agar with median values being 96% and 89%, respectively. On employing encapsulation-dehydration, greater variability between some validators was observed, with six labs observing recovery in 100% of the beads (84-95% of cells surviving) and one lab observing survival in 80% of the treated beads. Bead disruption followed by algal growth in agar was considered the most reliable and accurate method of assessing cell survival for encapsulation-dehydration."],["dc.identifier.isi","000250540800005"],["dc.identifier.pmid","18075705"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/50557"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Cryo Letters"],["dc.relation.issn","0143-2044"],["dc.title","The use of physical and virtual infrastructures for the validation of algal cryopreservation methods in international culture collections"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","231"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","CRYOLETTERS"],["dc.bibliographiccitation.lastpage","238"],["dc.bibliographiccitation.volume","26"],["dc.contributor.author","Day, J. G."],["dc.contributor.author","Benson, Erica E."],["dc.contributor.author","Harding, K."],["dc.contributor.author","Knowles, B."],["dc.contributor.author","Idowu, M."],["dc.contributor.author","Bremner, D."],["dc.contributor.author","Santos, L."],["dc.contributor.author","Santos, Fabricio R."],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Lorenz, M."],["dc.contributor.author","Lukesova, A."],["dc.contributor.author","Elster, J."],["dc.contributor.author","Lukavsky, J."],["dc.contributor.author","Herdman, M."],["dc.contributor.author","Rippka, R."],["dc.contributor.author","Hall, T."],["dc.date.accessioned","2018-11-07T09:00:51Z"],["dc.date.available","2018-11-07T09:00:51Z"],["dc.date.issued","2005"],["dc.description.abstract","Microalgae are one of the most biologically important elements of worldwide ecology and could be the source of diverse new products and medicines. COBRA (The COnservation of a vital european scientific and Biotechnological Resource: microAlgae and cyanobacteria) is the acronym for a European Union, RTD Infrastructures project (Contract No. QLRI-CT-2001-01645). This project is in the process of developing a European Biological Resource Centre based on existing algal culture collections. The COBRA project's central aim is to apply cryopreservation methodologies to microalgae and cyanobacteria, organisms that, to date, have proved difficult to conserve using cryogenic methods. In addition, molecular and biochemical stability tests have been developed to ensure that the equivalent strains of microorganisms supplied by the culture collections give high quality and consistent performance. Fundamental and applied knowledge of stress physiology form an essential component of the project and this is being employed to assist the optimisation. of methods for preserving a wide range of algal diversity. COBRA's \"Resource Centre\" utilises Information Technologies (IT) and Knowledge Management practices to assist project coordination, management and information dissemination and facilitate the generation of new knowledge pertaining to algal conservation. This review of the COBRA project will give a summary of current methodologies for cryopreservation of microalgae and procedures adopted within the COBRA project to enhance preservation techniques for this diverse group of organisms."],["dc.identifier.isi","000232226100003"],["dc.identifier.pmid","19827252"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/24268"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation.issn","0143-2044"],["dc.title","Cryopreservation and conservation of microalgae: The development of a pan-European scientific and biotechnological resource (The COBRA project)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","921"],["dc.bibliographiccitation.journal","Frontiers in Physiology"],["dc.bibliographiccitation.volume","9"],["dc.contributor.author","Bajerski, Felizitas"],["dc.contributor.author","Stock, Johanna"],["dc.contributor.author","Hanf, Benjamin"],["dc.contributor.author","Darienko, Tatyana"],["dc.contributor.author","Heine-Dobbernack, Elke"],["dc.contributor.author","Lorenz, Maike"],["dc.contributor.author","Naujox, Lisa"],["dc.contributor.author","Keller, E. R. J."],["dc.contributor.author","Schumacher, H. M."],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Eberth, Sonja"],["dc.contributor.author","Mock, Hans-Peter"],["dc.contributor.author","Kniemeyer, Olaf"],["dc.contributor.author","Overmann, Jörg"],["dc.date.accessioned","2019-07-22T14:46:42Z"],["dc.date.available","2019-07-22T14:46:42Z"],["dc.date.issued","2018"],["dc.description.abstract","In many natural environments, organisms get exposed to low temperature and/or to strong temperature shifts. Also, standard preservation protocols for live cells or tissues involve ultradeep freezing in or above liquid nitrogen (-196°C or -150°C, respectively). To which extent these conditions cause cold- or cryostress has rarely been investigated systematically. Using ATP content as an indicator of the physiological state of cells, we found that representatives of bacteria, fungi, algae, plant tissue, as well as plant and human cell lines exhibited similar responses during freezing and thawing. Compared to optimum growth conditions, the cellular ATP content of most model organisms decreased significantly upon treatment with cryoprotectant and cooling to up to -196°C. After thawing and a longer period of regeneration, the initial ATP content was restored or even exceeded the initial ATP levels. To assess the implications of cellular ATP concentration for the physiology of cryostress, cell viability was determined in parallel using independent approaches. A significantly positive correlation of ATP content and viability was detected only in the cryosensitive algae Chlamydomonas reinhardtii SAG 11-32b and Chlorella variabilis NC64A, and in plant cell lines of Solanum tuberosum. When comparing mesophilic with psychrophilic bacteria of the same genera, and cryosensitive with cryotolerant algae, ATP levels of actively growing cells were generally higher in the psychrophilic and cryotolerant representatives. During exposure to ultralow temperatures, however, psychrophilic and cryotolerant species showed a decline in ATP content similar to their mesophilic or cryosensitive counterparts. Nevertheless, psychrophilic and cryotolerant species attained better culturability after freezing. Cellular ATP concentrations and viability measurements thus monitor different features of live cells during their exposure to ultralow temperatures and cryostress."],["dc.identifier.doi","10.3389/fphys.2018.00921"],["dc.identifier.pmid","30065659"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/61835"],["dc.language.iso","en"],["dc.notes.intern","DeepGreen Import"],["dc.publisher","Frontiers Media S.A."],["dc.relation.eissn","1664-042X"],["dc.relation.issn","1664-042X"],["dc.rights","http://creativecommons.org/licenses/by/4.0/"],["dc.title","ATP Content and Cell Viability as Indicators for Cryostress Across the Diversity of Life"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","74"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Journal of Molecular Evolution"],["dc.bibliographiccitation.lastpage","84"],["dc.bibliographiccitation.volume","55"],["dc.contributor.author","Bhattacharya, Debashish"],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Helms, Gert"],["dc.date.accessioned","2018-11-07T10:22:13Z"],["dc.date.available","2018-11-07T10:22:13Z"],["dc.date.issued","2002"],["dc.description.abstract","One family within the Euascomycetes (Ascomycota), the lichen-forming Physciaceae, is particularly rich in nuclear ribosomal [r]DNA group I introns. We used phylogenetic analyses of group I introns and lichen-fungal host cells to address four questions about group I intron evolution in lichens, and generally in all eukaryotes: 1) Is intron spread in the lichens associated with the intimate association of the fungal and photosynthetic cells that make Lip the lichen thallus? 2) Are the Multiple group I introns in the lichen-fungi of independent origins, or have existing introns spread into novel sites in the rDNA? 3) If introns have moved to novel sites, then does the exon context of these sites provide insights into the mechanism of intron spread? and 4) What is the pattern of intron loss in the small subunit rDNA gene of lichen-fungi? Our analyses show that group I introns in the lichen-fungi and in the lichen-algae (and lichenized cyanobacteria) do not share a close evolutionary relationship, suggesting that these introns do not move between the symbionts. Many group I introns appear to have originated in the common ancestor of the Lecanorales, whereas others have spread within this lineage (particularly in the Physciaceae) putatively through reverse-splicing into novel rRNA sites. We suggest that the evolutionary history of most lichen-fungal group I introns is characterized by rare gains followed by extensive losses in descendants, resulting in a sporadic intron distribution. Detailed phylogenetic analyses of the introns and host cells are required, therefore, to distinguish this scenario from the alternative hypothesis of widespread and independent intron gains in the different lichen-fungal lineages."],["dc.identifier.doi","10.1007/s00239-001-2305-x"],["dc.identifier.isi","000176243200007"],["dc.identifier.pmid","12165844"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42237"],["dc.language.iso","en"],["dc.notes.status","final"],["dc.notes.submitter","Najko"],["dc.relation.issn","0022-2844"],["dc.title","Vertical evolution and intragenic spread of lichen-fungal group I introns"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","229"],["dc.bibliographiccitation.issue","2"],["dc.bibliographiccitation.journal","Microbial Ecology"],["dc.bibliographiccitation.lastpage","247"],["dc.bibliographiccitation.volume","57"],["dc.contributor.author","Buedel, Burkhard"],["dc.contributor.author","Darienko, Tatyana"],["dc.contributor.author","Deutschewitz, Kirstin"],["dc.contributor.author","Dojani, Stephanie"],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Mohr, Kathrin I."],["dc.contributor.author","Salisch, Mario"],["dc.contributor.author","Reisser, Werner"],["dc.contributor.author","Weber, Bettina"],["dc.date.accessioned","2018-11-07T08:33:14Z"],["dc.date.available","2018-11-07T08:33:14Z"],["dc.date.issued","2009"],["dc.description.abstract","Biological soil crusts (BSCs) are found in all dryland regions of the world, including the polar regions. They are also known to occur in the southern African region. Although there were a number of case studies on BSCs from that region, we did not know if they are a normal part of the vegetation cover or just a phenomenon that occasionally occurs here and there. In order to investigate diversity, distribution patterns, and the driving factors of both, we followed a random sampling system of observatories along a transect, stretching from the Namibian-Angolan border down south to the Cape Peninsula, covering seven different major biomes. Biological soil crusts were found to occur in six out of seven biomes. Despite the fact that soil-dwelling algae occurred in the Fynbos biome, crust formation was not observed for hitherto unknown reasons. Seven BSC types were distinguished on the basis of morphology and taxonomic composition: three of them were cyanobacteria-dominated, one with additional chlorolichens, two with bryophytes, one hypolithic type restricted to quartz gravel pavements, and the unique lichen fields of the Namib Desert. Besides 29 green algal species in 21 genera, one heterokont alga, 12 cyanolichens, 14 chlorolichens, two genera of liverworts, and three genera of mosses, these crusts are positioned among the most diverse BSCs worldwide mainly because of the unusual high cyanobacterial species richness comprising 58 species in 21 genera. They contribute considerably to the biodiversity of arid and semi-arid bioregions. Taxonomic diversity of cyanobacteria was significantly higher in the winter rain zone than in the summer rain zone (54 versus 32 species). The soil photosynthetic biomass (chlorophyll(a)/m(2)), the carbon content of the soil and the number of BSC types were significantly higher in the winter rain zone (U (27, 29) = 215.0, p = 0.004 [chl(a)]; U (21, 21) = 135.0, p = 0.031 [C]; U (27, 29) = 261.5, p = 0.028 [BSC types]; excluding the fog-dominated Namib biome). The winter rain zone is characterized by a lower precipitation amount, but a higher rain frequency with the number of rainy days more evenly distributed over the year. The dry period is significantly shorter per year in the winter rain zone (U (8, 9) = 5.0, p = 0.003). We conclude that rain frequency and duration of dry periods rather than the precipitation amount is the main factor for BSC growth and succession. Nitrogen content of the soils along the transect was generally very low and correlated with soil carbon content. There was a weak trend that an increasing proportion of silt and clay (< 0.63 mm) in the soil is associated with higher values of BSC chlorophyll content (Pearson correlation coefficient = 0.314, p = 0.237). Furthermore, we found a significant positive correlation between silt and clay and the number of BSC types (Pearson correlation coefficient = 0.519, p = 0.039), suggesting that fine grain-size promotes BSC succession and their biomass content. Lichens and bryophytes occurred in BSCs with lower disturbance frequencies (e.g. trampling) only. Crust thickness and chlorophyll content increased significantly from crusts of the early successional type to the late successional crust types. From our results, we conclude that BSCs are a normal and frequent element of the vegetation in arid and semi-arid southwestern Africa, and that rain frequency and duration of dry periods rather than the precipitation amount are the key factors for the development, differentiation and compsition of BSCs."],["dc.description.sponsorship","German Ministry of Education and Research (BMBF)"],["dc.identifier.doi","10.1007/s00248-008-9449-9"],["dc.identifier.isi","000262829500003"],["dc.identifier.pmid","18850242"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/17527"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0095-3628"],["dc.title","Southern African Biological Soil Crusts are Ubiquitous and Highly Diverse in Drylands, Being Restricted by Rainfall Frequency"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","406"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Protist"],["dc.bibliographiccitation.lastpage","431"],["dc.bibliographiccitation.volume","169"],["dc.contributor.author","Mikhailyuk, Tatiana"],["dc.contributor.author","Lukešová, Alena"],["dc.contributor.author","Glaser, Karin"],["dc.contributor.author","Holzinger, Andreas"],["dc.contributor.author","Obwegeser, Sabrina"],["dc.contributor.author","Nyporko, Svetlana"],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Karsten, Ulf"],["dc.date.accessioned","2020-12-10T15:20:55Z"],["dc.date.available","2020-12-10T15:20:55Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1016/j.protis.2018.03.002"],["dc.identifier.issn","1434-4610"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/72859"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","New Taxa of Streptophyte Algae (Streptophyta) from Terrestrial Habitats Revealed Using an Integrative Approach"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","460"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","CRYOLETTERS"],["dc.bibliographiccitation.lastpage","472"],["dc.bibliographiccitation.volume","31"],["dc.contributor.author","Harding, Keith"],["dc.contributor.author","Mueller, Julia"],["dc.contributor.author","Timmermann, Hella"],["dc.contributor.author","Lorenz, Maike"],["dc.contributor.author","Day, John G."],["dc.contributor.author","Friedl, Thomas"],["dc.date.accessioned","2018-11-07T08:37:25Z"],["dc.date.available","2018-11-07T08:37:25Z"],["dc.date.issued","2010"],["dc.description.abstract","An encapsulation/dehydration procedure was developed for Euglena gracilis Klebs as a 'model alga' to examine various cryoprotective regimes combined with controlled rate cooling to cryopreserve other Euglenoid taxa. Cryoprotective variables were optimised to enable reproducible growth following a combination of alginate encapsulation, sucrose osmotic dehydration, air desiccation, methanol treatment, cooling to -40 degrees C and plunging into liquid nitrogen (LN). Amplified Fragment Length Polymorphism (AFLP) analysis was adapted to: (i) verify algal identity by discriminating between different Euglenoids and (ii) examine the genetic stability of algal cultures prior to various stages of cryoprotective treatments and following exposure to LN. AFLPs were highly reproducible (>99%) as reliable diagnostic markers, where a single DNA fragment change accounted for similar to 0.4% of the detectable variation in an AFLP pattern. AFLP changes were detected in cryoprotective treatments following LN exposure. Successive stages of the dehydration and desiccation treatments did not accumulate AFLP changes indicating these are random events."],["dc.identifier.isi","000286697900004"],["dc.identifier.pmid","21410015"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/18528"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Cryo Letters"],["dc.relation.issn","0143-2044"],["dc.title","ENCAPSULATION DEHYDRATION COLLIGATIVE CRYOPROTECTIVE STRATEGIES AND AMPLIFIED FRAGMENT LENGTH POLYMORPHISM MARKERS TO VERIFY THE IDENTITY AND GENETIC STABILITY OF EUGLENOIDS FOLLOWING CRYOPRESERVATION"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","125697"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Protist"],["dc.bibliographiccitation.volume","170"],["dc.contributor.author","Wang, Sibo"],["dc.contributor.author","Li, Linzhou"],["dc.contributor.author","Xu, Yan"],["dc.contributor.author","Melkonian, Barbara"],["dc.contributor.author","Lorenz, Maike"],["dc.contributor.author","Friedl, Thomas"],["dc.contributor.author","Petersen, Morten"],["dc.contributor.author","Sahu, Sunil Kumar"],["dc.contributor.author","Melkonian, Michael"],["dc.contributor.author","Liu, Huan"],["dc.date.accessioned","2020-12-10T15:20:56Z"],["dc.date.available","2020-12-10T15:20:56Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1016/j.protis.2019.125697"],["dc.identifier.issn","1434-4610"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/72861"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","The Draft Genome of the Small, Spineless Green Alga Desmodesmus costato-granulatus (Sphaeropleales, Chlorophyta)"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]