Rubén G. G. Mateo

Dr. Rubén G. G. Mateo

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Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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14 February 2017 in Ecography
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VCValeria Di Cola
Valeria Di Cola
OBOlivier Broennimann
Olivier Broennimann
BPBlaise Petitpierre
Blaise Petitpierre
FBFrank T. Breiner
Frank T. Breiner
MDManuela D'Amen
Manuela D'Amen
AGAntoine Guisan
Antoine Guisan

1 September 2015 in Ecological Modelling
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Journal Article
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EMElena Moreno-Amat
Elena Moreno-Amat
RMRubén G. G. Mateo
Rubén G. G. Mateo
DNDiego Nieto-Lugilde
Diego Nieto-Lugilde
NMNaia Morueta-Holme
Naia Morueta-Holme
Jens-Christian SvenningJens-Christian Svenning
Jens-Christian Svenning
IGIgnacio García-Amorena
Ignacio García-Amorena

18 January 2010 in Diversity and Distributions
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Journal Article
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RMRubén G. G. Mateo
Rubén G. G. Mateo
TCThomas B. Croat
Thomas B. Croat
AFAngel M. Felicisimo
Angel M. Felicisimo
JMJesús Muñoz
Jesús Muñoz
Aim  The presence‐only data stored in natural history collections is the most important source of information available regarding the distribution of organisms. These data and profile techniques can be used to generate species distribution models (SDMs), but pseudo‐absences must be generated to use group discriminative techniques. In this study, we evaluated whether the SDMs generated with pseudo‐absences are reliable and also if there are differences in the results obtained with profile and group discriminative techniques.Location  Ecuador, South America.Methods  The SDMs were generated with a training data set for each of the five species of Anthurium and six different methods: two profile techniques (BIOCLIM and Gower’s distance index), three group discriminative techniques [logistic multiple regression (LMR), multivariate adaptative regression splines (MARS) and Maxent] and a mixed modelling approach genetic algorithm for rule‐set production (GARP), which employs a combination of profile and group discriminative techniques and generates its own pseudo‐absences. For LMR, MARS and Maxent, three types of absences were generated: (1) random pseudo‐absences in equal number to presences and excluding a buffer area around presences (except for Maxent, which assumes that this background sample includes presences), (2) a large number (10,000) of random pseudo‐absences, also excluding a buffer area around each presence and (3) ‘target‐group absences’ (TGA), consisting of sites where other species of the group have been collected by the specialist, but not the species being modelled. To compare the predictive performance of the SDMs, the area under the curve statistic was calculated using an independent testing data set for each species.Results  MARS, Maxent and LMR produce better results than the profile techniques. The models created with TGA are generally more accurate than those generated with pseudo‐absences.Main conclusions  The advantages and disadvantages of different options for using pseudo‐absences and TGA with profile and group discriminative modelling techniques are explained and recommendations are made for the future.

1 June 2011 in Revista chilena de historia natural
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RMRubén G. G. Mateo
Rubén G. G. Mateo
AFAngel M. Felicisimo
Angel M. Felicisimo
JMJesús Muñoz
Jesús Muñoz
En los últimos años se ha generalizado una nueva herramienta que permite analizar objetivamente los patrones espaciales de presencia de organismos: los modelos de distribución de especies. Estos modelos se basan en procedimientos estadísticos y cartográficos que partiendo de datos reales de presencia permiten inferir zonas potencialmente idóneas en función de sus características ambientales. Los datos de colecciones de historia natural pueden ser utilizados para este fin adquiriendo así una nueva utilidad. Los modelos han evolucionado desde su aplicación a especies aisladas hasta análisis de cientos o miles de taxones para combinarlos en el análisis de la biodiversidad y riqueza específica. En este trabajo se hace una revisión sobre la variedad de métodos utilizables, sus potencialidades e inconvenientes y los factores limitantes que influyen en la interpretación de lo que los modelos de distribución significan.

5 November 2020 in Nature Communications
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FZF. Zanatta
F. Zanatta
RER. Engler
R. Engler
FCF. Collart
F. Collart
OBO. Broennimann
O. Broennimann
RMRubén G. G. Mateo
Rubén G. G. Mateo
AVAlain Vanderpoorten
Alain Vanderpoorten
The extent to which species can balance out the loss of suitable habitats due to climate warming by shifting their ranges is an area of controversy. Here, we assess whether highly efficient wind-dispersed organisms like bryophytes can keep-up with projected shifts in their areas of suitable climate. Using a hybrid statistical-mechanistic approach accounting for spatial and temporal variations in both climatic and wind conditions, we simulate future migrations across Europe for 40 bryophyte species until 2050. The median ratios between predicted range loss vs expansion by 2050 across species and climate change scenarios range from 1.6 to 3.3 when only shifts in climatic suitability were considered, but increase to 34.7–96.8 when species dispersal abilities are added to our models. This highlights the importance of accounting for dispersal restrictions when projecting future distribution ranges and suggests that even highly dispersive organisms like bryophytes are not equipped to fully track the rates of ongoing climate change in the course of the next decades.

2 August 2024 in Ecography
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Vítězslav MoudrýVítězslav Moudrý
Vítězslav Moudrý
Manuele BazzichettoManuele Bazzichetto
Manuele Bazzichetto
RRRuben Remelgado
Ruben Remelgado
RDRodolphe Devillers
Rodolphe Devillers
JLJonathan Lenoir
Jonathan Lenoir
Petra ŠímováPetra Šímová
Petra Šímová
Species distribution models (SDMs) have proven valuable in filling gaps in our knowledge of species occurrences. However, despite their broad applicability, SDMs exhibit critical shortcomings due to limitations in species occurrence data. These limitations include, in particular, issues related to sample size, positional uncertainty, and sampling bias. In addition, it is widely recognised that the quality of SDMs as well as the approaches used to mitigate the impact of the aforementioned data limitations depend on species ecology. While numerous studies have evaluated the effects of these data limitations on SDM performance, a synthesis of their results is lacking. However, without a comprehensive understanding of their individual and combined effects, our ability to predict the influence of these issues on the quality of modelled species–environment associations remains largely uncertain, limiting the value of model outputs. In this paper, we review studies that have evaluated the effects of sample size, positional uncertainty, sampling bias, and species ecology on SDMs outputs. We build upon their findings to provide recommendations for the critical assessment of species data intended for use in SDMs.