Markus Pfenninger

Prof. Dr. Markus Pfenninger

Senckenberg Biodiversity & Climate Research Centre, Molecular Ecology Group, Georg-Voigt Straße 14-16, D-60325 Frankfurt am Main, Germany
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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

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

Representative Publications

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20 December 2012 in Molecular Ecology
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Journal Article
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SPSteffen Pauls
Steffen Pauls
CNCarsten Nowak
Carsten Nowak
MBMiklós Bálint
Miklós Bálint
MPMarkus Pfenninger
Markus Pfenninger

1 January 2007 in BMC Ecology and Evolution
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MPMarkus Pfenninger
Markus Pfenninger
KSKlaus Schwenk
Klaus Schwenk
Cryptic species are two or more distinct but morphologically similar species that were classified as a single species. During the past two decades we observed an exponential growth of publications on cryptic species. Recently published reviews have demonstrated cryptic species have profound consequences on many biological disciplines. It has been proposed that their distribution is non-random across taxa and biomes.

14 January 2020 in Evolution Letters
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AWAnn-Marie Waldvogel
Ann-Marie Waldvogel
BFBarbara Feldmeyer
Barbara Feldmeyer
GRGregor Rolshausen
Gregor Rolshausen
MEMoises Exposito-Alonso
Moises Exposito-Alonso
CRChristian Rellstab
Christian Rellstab
MPMarkus Pfenninger
Markus Pfenninger
Global climate change (GCC) increasingly threatens biodiversity through the loss of species, and the transformation of entire ecosystems. Many species are challenged by the pace of GCC because they might not be able to respond fast enough to changing biotic and abiotic conditions. Species can respond either by shifting their range, or by persisting in their local habitat. If populations persist, they can tolerate climatic changes through phenotypic plasticity, or genetically adapt to changing conditions depending on their genetic variability and census population size to allow for de novo mutations. Otherwise, populations will experience demographic collapses and species may go extinct. Current approaches to predicting species responses to GCC begin to combine ecological and evolutionary information for species distribution modelling. Including an evolutionary dimension will substantially improve species distribution projections which have not accounted for key processes such as dispersal, adaptive genetic change, demography, or species interactions. However, eco-evolutionary models require new data and methods for the estimation of a species' adaptive potential, which have so far only been available for a small number of model species. To represent global biodiversity, we need to devise large-scale data collection strategies to define the ecology and evolutionary potential of a broad range of species, especially of keystone species of ecosystems. We also need standardized and replicable modelling approaches that integrate these new data to account for eco-evolutionary processes when predicting the impact of GCC on species' survival. Here, we discuss different genomic approaches that can be used to investigate and predict species responses to GCC. This can serve as guidance for researchers looking for the appropriate experimental setup for their particular system. We furthermore highlight future directions for moving forward in the field and allocating available resources more effectively, to implement mitigation measures before species go extinct and ecosystems lose important functions.

9 September 2006 in Oecologia
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TBT. Burgmer
T. Burgmer
HHH. Hillebrand
H. Hillebrand
MPMarkus Pfenninger
Markus Pfenninger

18 October 2011 in Zoologica Scripta
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MJMartin Jansen
Martin Jansen
RBRebecca Bloch
Rebecca Bloch
ASArne Schulze
Arne Schulze
MPMarkus Pfenninger
Markus Pfenninger

16 June 2011 in BMC Genomics
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BFBarbara Feldmeyer
Barbara Feldmeyer
CWChristopher W Wheat
Christopher W Wheat
NKNicolas Krezdorn
Nicolas Krezdorn
BRBjörn Rotter
Björn Rotter
MPMarkus Pfenninger
Markus Pfenninger
Until recently, read lengths on the Solexa/Illumina system were too short to reliably assemble transcriptomes without a reference sequence, especially for non-model organisms. However, with read lengths up to 100 nucleotides available in the current version, an assembly without reference genome should be possible. For this study we created an EST data set for the common pond snail Radix balthica by Illumina sequencing of a normalized transcriptome. Performance of three different short read assemblers was compared with respect to: the number of contigs, their length, depth of coverage, their quality in various BLAST searches and the alignment to mitochondrial genes.