Santiago Madriñán

Dr. Santiago Madriñán


Research Focus & Metrics

Academic Career Length

39Years (1988-Present)

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

Representative Publications

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1 May 2007 in Taxon
Verified
Journal Article
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MCMark W. Chase
Mark W. Chase
RCRobyn S. Cowan
Robyn S. Cowan
PHPeter M. Hollingsworth
Peter M. Hollingsworth
Cássio van den BergCássio van den Berg
Cássio van den Berg
SMSantiago Madriñán
Santiago Madriñán
MWMike Wilkinson
Mike Wilkinson

1 January 2013 in Frontiers in Genetics
Verified
Journal Article
Open access
PDF file
SMSantiago Madriñán
Santiago Madriñán
Andrés J. CortésAndrés J. Cortés
Andrés J. Cortés
JRJames E. Richardson
James E. Richardson
Understanding the processes that cause speciation is a key aim of evolutionary biology. Lineages or biomes that exhibit recent and rapid diversification are ideal model systems for determining these processes. Species rich biomes reported to be of relatively recent origin, i.e., since the beginning of the Miocene, include Mediterranean ecosystems such as the California Floristic Province, oceanic islands such as the Hawaiian archipelago and the Neotropical high elevation ecosystem of the Páramos. Páramos constitute grasslands above the forest tree-line (at elevations of c. 2800–4700 m) with high species endemism. Organisms that occupy this ecosystem are a likely product of unique adaptations to an extreme environment that evolved during the last three to five million years when the Andes reached an altitude that was capable of sustaining this type of vegetation. We compared net diversification rates of lineages in fast evolving biomes using 73 dated molecular phylogenies. Based on our sample, we demonstrate that average net diversification rates of Páramo plant lineages are faster than those of other reportedly fast evolving hotspots and that the faster evolving lineages are more likely to be found in Páramos than the other hotspots. Páramos therefore represent the ideal model system for studying diversification processes. Most of the speciation events that we observed in the Páramos (144 out of 177) occurred during the Pleistocene possibly due to the effects of species range contraction and expansion that may have resulted from the well-documented climatic changes during that period. Understanding these effects will assist with efforts to determine how future climatic changes will impact plant populations.

1 March 2012 in Molecular Phylogenetics and Evolution
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Journal Article
Closed access
NPNelsy Rocío Pinto-Sánchez
Nelsy Rocío Pinto-Sánchez
RIRoberto Ibáñez
Roberto Ibáñez
SMSantiago Madriñán
Santiago Madriñán
OSOris I. Sanjur
Oris I. Sanjur
EBEldredge Bermingham
Eldredge Bermingham
Andrew CrawfordAndrew Crawford
Andrew Crawford

1 January 2013 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
Nicolai NürkNicolai Nürk
Nicolai Nürk
SMSantiago Madriñán
Santiago Madriñán
MCMark A. Carine
Mark A. Carine
MCMark W. Chase
Mark W. Chase
FBFrank R. Blattner
Frank R. Blattner

3 May 2013 in PLOS ONE
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Journal Article
Open access
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Andrés J. CortésAndrés J. Cortés
Andrés J. Cortés
FMFredy A Monserrate
Fredy A Monserrate
JRJulián Ramírez-Villegas
Julián Ramírez-Villegas
SMSantiago Madriñán
Santiago Madriñán
MBMatthew W Blair
Matthew W Blair
Reliable estimations of drought tolerance in wild plant populations have proved to be challenging and more accessible alternatives are desirable. With that in mind, an ecological diversity study was conducted based on the geographical origin of 104 wild common bean accessions to estimate drought tolerance in their natural habitats. Our wild population sample covered a range of mesic to very dry habitats from Mexico to Argentina. Two potential evapotranspiration models that considered the effects of temperature and radiation were coupled with the precipitation regimes of the last fifty years for each collection site based on geographical information system analysis. We found that wild accessions were distributed among different precipitation regimes following a latitudinal gradient and that habitat ecological diversity of the collection sites was associated with natural sub-populations. We also detected a broader geographic distribution of wild beans across ecologies compared to cultivated common beans in a reference collection of 297 cultivars. Habitat drought stress index based on the Thornthwaite potential evapotranspiration model was equivalent to the Hamon estimator. Both ecological drought stress indexes would be useful together with population structure for the genealogical analysis of gene families in common bean, for genome-wide genetic-environmental associations, and for postulating the evolutionary history and diversification processes that have occurred for the species. Finally, we propose that wild common bean should be taken into account to exploit variation for drought tolerance in cultivated common bean which is generally considered susceptible as a crop to drought stress.

3 February 2015 in New Phytologist
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Journal Article
Closed access
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ESElizabeth Spriggs
Elizabeth Spriggs
WCWendy L. Clement
Wendy L. Clement
PSPatrick W. Sweeney
Patrick W. Sweeney
SMSantiago Madriñán
Santiago Madriñán
EEErika J. Edwards
Erika J. Edwards
MDMichael J. Donoghue
Michael J. Donoghue