József Geml

Dr. József Geml

Eszterházy Károly Catholic University, Eger, Heves, Hungary
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orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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28 November 2014 in Science
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LTLeho Tedersoo
Leho Tedersoo
MBMohammad Bahram
Mohammad Bahram
SPSergei Põlme
Sergei Põlme
UKUrmas Kõljalg
Urmas Kõljalg
NYNourou S. Yorou
Nourou S. Yorou
KAKessy Abarenkov
Kessy Abarenkov
Fungi play major roles in ecosystem processes, but the determinants of fungal diversity and biogeographic patterns remain poorly understood. Using DNA metabarcoding data from hundreds of globally distributed soil samples, we demonstrate that fungal richness is decoupled from plant diversity. The plant-to-fungus richness ratio declines exponentially toward the poles. Climatic factors, followed by edaphic and spatial variables, constitute the best predictors of fungal richness and community composition at the global scale. Fungi show similar latitudinal diversity gradients to other organisms, with several notable exceptions. These findings advance our understanding of global fungal diversity patterns and permit integration of fungi into a general macroecological framework.

18 March 2019 in Nature Ecology & Evolution
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TVTorda Varga
Torda Varga
KKKrisztina Krizsán
Krisztina Krizsán
CFCsenge Földi
Csenge Földi
BDBálint Dima
Bálint Dima
MSMarisol Sánchez-García
Marisol Sánchez-García
LNLaszlo G. Nagy
Laszlo G. Nagy
Mushroom-forming fungi (Agaricomycetes) have the greatest morphological diversity and complexity of any group of fungi. They have radiated into most niches and fulfil diverse roles in the ecosystem, including wood decomposers, pathogens or mycorrhizal mutualists. Despite the importance of mushroom-forming fungi, large-scale patterns of their evolutionary history are poorly known, in part due to the lack of a comprehensive and dated molecular phylogeny. Here, using multigene and genome-based data, we assemble a 5,284-species phylogenetic tree and infer ages and broad patterns of speciation/extinction and morphological innovation in mushroom-forming fungi. Agaricomycetes started a rapid class-wide radiation in the Jurassic, coinciding with the spread of (sub)tropical coniferous forests and a warming climate. A possible mass extinction, several clade-specific adaptive radiations and morphological diversification of fruiting bodies followed during the Cretaceous and the Paleogene, convergently giving rise to the classic toadstool morphology, with a cap, stalk and gills (pileate-stipitate morphology). This morphology is associated with increased rates of lineage diversification, suggesting it represents a key innovation in the evolution of mushroom-forming fungi. The increase in mushroom diversity started during the Mesozoic-Cenozoic radiation event, an era of humid climate when terrestrial communities dominated by gymnosperms and reptiles were also expanding.

7 June 2011 in IMA Fungus
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DHDavid Leslie Hawksworth
David Leslie Hawksworth
PCPedro W. Crous
Pedro W. Crous
SRScott A. Redhead
Scott A. Redhead
DRDon R. Reynolds
Don R. Reynolds
RSRobert A. Samson
Robert A. Samson
Ning ZhangNing Zhang
Ning Zhang
The Amsterdam Declaration on Fungal Nomenclature was agreed at an international symposium convened in Amsterdam on 19–20 April 2011 under the auspices of the International Commission on the Taxonomy of Fungi (ICTF). The purpose of the symposium was to address the issue of whether or how the current system of naming pleomorphic fungi should be maintained or changed now that molecular data are routinely available. The issue is urgent as mycologists currently follow different practices, and no consensus was achieved by a Special Committee appointed in 2005 by the International Botanical Congress to advise on the problem. The Declaration recognizes the need for an orderly transitition to a single-name nomenclatural system for all fungi, and to provide mechanisms to protect names that otherwise then become endangered. That is, meaning that priority should be given to the first described name, except where that is a younger name in general use when the first author to select a name of a pleomorphic monophyletic genus is to be followed, and suggests controversial cases are referred to a body, such as the ICTF, which will report to the Committee for Fungi. If appropriate, the ICTF could be mandated to promote the implementation of the Declaration. In addition, but not forming part of the Declaration, are reports of discussions held during the symposium on the governance of the nomenclature of fungi, and the naming of fungi known only from an environmental nucleic acid sequence in particular. Possible amendments to the Draft BioCode (2011) to allow for the needs of mycologists are suggested for further consideration, and a possible example of how a fungus only known from the environment might be described is presented.

12 August 2015 in Nature
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VMVincent S. F. T. Merckx
Vincent S. F. T. Merckx
KHKasper P. Hendriks
Kasper P. Hendriks
KBKevin K. Beentjes
Kevin K. Beentjes
CMConstantijn B. Mennes
Constantijn B. Mennes
LBLeontine E. Becking
Leontine E. Becking
MSMenno Schilthuizen
Menno Schilthuizen

29 July 2013 in PLOS ONE
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MSMartijn Staats
Martijn Staats
RERoy H. J. Erkens
Roy H. J. Erkens
BVBart T. L. H. Van De Vossenberg
Bart T. L. H. Van De Vossenberg
JWJan J. Wieringa
Jan J. Wieringa
KKKen Kraaijeveld
Ken Kraaijeveld
FBFreek T. Bakker
Freek T. Bakker
Unlocking the vast genomic diversity stored in natural history collections would create unprecedented opportunities for genome-scale evolutionary, phylogenetic, domestication and population genomic studies. Many researchers have been discouraged from using historical specimens in molecular studies because of both generally limited success of DNA extraction and the challenges associated with PCR-amplifying highly degraded DNA. In today's next-generation sequencing (NGS) world, opportunities and prospects for historical DNA have changed dramatically, as most NGS methods are actually designed for taking short fragmented DNA molecules as templates. Here we show that using a standard multiplex and paired-end Illumina sequencing approach, genome-scale sequence data can be generated reliably from dry-preserved plant, fungal and insect specimens collected up to 115 years ago, and with minimal destructive sampling. Using a reference-based assembly approach, we were able to produce the entire nuclear genome of a 43-year-old Arabidopsis thaliana (Brassicaceae) herbarium specimen with high and uniform sequence coverage. Nuclear genome sequences of three fungal specimens of 22–82 years of age (Agaricus bisporus, Laccaria bicolor, Pleurotus ostreatus) were generated with 81.4–97.9% exome coverage. Complete organellar genome sequences were assembled for all specimens. Using de novo assembly we retrieved between 16.2–71.0% of coding sequence regions, and hence remain somewhat cautious about prospects for de novo genome assembly from historical specimens. Non-target sequence contaminations were observed in 2 of our insect museum specimens. We anticipate that future museum genomics projects will perhaps not generate entire genome sequences in all cases (our specimens contained relatively small and low-complexity genomes), but at least generating vital comparative genomic data for testing (phylo)genetic, demographic and genetic hypotheses, that become increasingly more horizontal. Furthermore, NGS of historical DNA enables recovering crucial genetic information from old type specimens that to date have remained mostly unutilized and, thus, opens up a new frontier for taxonomic research as well.

14 March 2018 in PLOS Biology
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STScott A. Thomson
Scott A. Thomson
RPRichard L. Pyle
Richard L. Pyle
SAShane T. Ahyong
Shane T. Ahyong
MAMiguel Alonso-Zarazaga
Miguel Alonso-Zarazaga
JAJoe Ammirati
Joe Ammirati
HZHong-Zhang Zhou
Hong-Zhang Zhou