Diego MICAELA Baldo

Dr. Diego MICAELA Baldo


Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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3 August 2011 in Global Change Biology
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HDHelder Duarte
Helder Duarte
Miguel TejedoMiguel Tejedo
Miguel Tejedo
MKMarco Katzenberger
Marco Katzenberger
FMFederico Marangoni
Federico Marangoni
DBDiego MICAELA Baldo
Diego MICAELA Baldo
AGAlejandro Gonzalez‐Voyer
Alejandro Gonzalez‐Voyer
Predicting the biodiversity impacts of global warming implies that we know where and with what magnitude these impacts will be encountered. Amphibians are currently the most threatened vertebrates, mainly due to habitat loss and to emerging infectious diseases. Global warming may further exacerbate their decline in the near future, although the impact might vary geographically. We predicted that subtropical amphibians should be relatively susceptible to warming‐induced extinctions because their upper critical thermal limits (CTmax) might be only slightly higher than maximum pond temperatures (Tmax). We tested this prediction by measuringCTmaxandTmaxfor 47 larval amphibian species from two thermally distinct subtropical communities (the warm community of the Gran Chaco and the cool community of Atlantic Forest, northern Argentina), as well as from one European temperate community. Upper thermal tolerances of tadpoles were positively correlated (controlling for phylogeny) with maximum pond temperatures, although the slope was steeper in subtropical than in temperate species.CTmaxvalues were lowest in temperate species and highest in the subtropical warm community, which paradoxically, had very low warming tolerance (CTmax–Tmax) and therefore may be prone to future local extinction from acute thermal stress if rising pondTmaxsoon exceeds theirCTmax. Canopy‐protected subtropical cool species have larger warming tolerance and thus should be less impacted by peak temperatures. Temperate species are relatively secure to warming impacts, except for late breeders with low thermal tolerance, which may be exposed to physiological thermal stress in the coming years.

1 November 2015 in Biological Conservation
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JNJavier Nori
Javier Nori
PLPriscila Lemes
Priscila Lemes
Nicolas Urbina-CardonaNicolas Urbina-Cardona
Nicolas Urbina-Cardona
DBDiego MICAELA Baldo
Diego MICAELA Baldo
JLJulián Lescano
Julián Lescano
RLRafael Loyola
Rafael Loyola

1 December 2014 in South American Journal of Herpetology
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JFJulián Faivovich
Julián Faivovich
LNLaura Nicoli
Laura Nicoli
BBBoris L. Blotto
Boris L. Blotto
MPMartín O. Pereyra
Martín O. Pereyra
DBDiego MICAELA Baldo
Diego MICAELA Baldo
CHCélio F.B. Haddad
Célio F.B. Haddad
The horned frog family, Ceratophryidae, currently comprises three genera and 12 extant species, distributed from the Caribbean lowlands to the Pampean grasslands. Horned frogs are fossorial species that are remarkable in terms of their adult and larval morphology, karyotype, behavior, and other aspects of their biology. In this paper we present a molecular phylogenetic analysis with the goals of: (1) exploring the relationships among the species of Ceratophryidae; (2) studying the evolution of polyploidy; (3) studying the evolution of cocoon formation and larval development duration associated with surviving in semiarid environments; and (4) reviewing the ceratophryid fossil record that could be relevant as calibration points in molecular divergence estimations. The analysis included 11 of the 12 extant species and, when possible, multiple exemplars per species, as well as multiple outgroups. Sequence data were obtained on seven mitochondrial and six nuclear genes for up to 8200 bp per specimen....

1 March 2021 in Bulletin of the American Museum of Natural History
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MPMartín O. Pereyra
Martín O. Pereyra
BBBoris L. Blotto
Boris L. Blotto
DBDiego MICAELA Baldo
Diego MICAELA Baldo
JCJuan Chaparro
Juan Chaparro
SRSantiago R. Ron
Santiago R. Ron
JFJulián Faivovich
Julián Faivovich
True toads of the genus Rhinella are among the most common and diverse group of Neotropical anurans. These toads are widely distributed throughout South America, inhabiting a great diversity of environments and ecoregions. Currently, however, the genus is defined solely on the basis of molecular characters, and it lacks a proper diagnosis. Although some phenetic species groups have traditionally been recognized within Rhinella, the monophyly of some of them have been rejected in previous phylogenetic analyses, and many species remain unassigned to these poorly defined groups. Additionally, the identity and taxonomy of several species are problematic and hinder the specific recognition and description of undescribed taxa. In this work, we first perform phylogenetic analyses of separate mitochondrial and nuclear datasets to test the possible occurrence of hybridization and/or genetic introgression in the genus. The comparative analysis of both datasets revealed unidirectional mitochondrial introgressions of an unknown parental species into R. horribilis (“ghost introgression”) and of R. dorbignyi into R. bernardoi; therefore, the mitochondrial and nuclear datasets of these species were considered separately in subsequent analyses. We performed total-evidence phylogenetic analyses that included revised molecular (four mitochondrial and five nuclear genes) and phenotypic (90 characters) datasets for 83 nominal species of Rhinella, plus several undescribed and problematic species and multiple outgroups. Results demonstrate that Rhinella was nonmonophyletic due to the position of R. ceratophrys, which was recovered as the sister taxon of Rhaebo nasicus with strong support. Among our outgroups, the strongly supported Anaxyrus + Incilius is the sister clade of all other species of Rhinella. Once R. ceratophrys is excluded, the genus Rhinella is monophyletic, well supported, and composed of two major clades. One of these is moderately supported and includes species of the former R. spinulosa Group (including R. gallardoi); the monophyletic R. granulosa, R. crucifer, and R. marina Groups; and a clade composed of the mitochondrial sequences of R. horribilis. The other major clade is strongly supported and composed of all the species from the non-monophyletic R. veraguensis and R. margaritifera Groups, the former R. acrolopha Group, and R. sternosignata. Consistent with these results, we define eight species groups of Rhinella that are mostly diagnosed by phenotypic synapomorphies in addition to a combination of morphological character states. Rhinella sternosignata is the only species that remains unassigned to any group. We also synonymize nine species, treat three former subspecies as full species, and suggest that 15 lineages represent putative undescribed species. Lastly, we discuss the apparently frequent occurrence of hybridization, deep mitochondrial divergence, and “ghost introgression”; the incomplete phenotypic evidence (including putative character systems that could be used for future phylogenetic analyses); and the validity of the known fossil record of Rhinella as a source of calibration points for divergence dating analyses.

6 December 2011 in Cladistics
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CSClaudia Szumik
Claudia Szumik
LALone Aagesen
Lone Aagesen
DCDolores Casagranda
Dolores Casagranda
VAVanesa Arzamendia
Vanesa Arzamendia
DBDiego MICAELA Baldo
Diego MICAELA Baldo
FZFernando O. Zuloaga
Fernando O. Zuloaga
The idea of an area of endemism implies that different groups of plants and animals should have largely coincident distributions. This paper analyses an area of 1152 000 km2, between parallels 21 and 32°S and meridians 70 and 53°W to examine whether a large and taxonomically diverse data set actually displays areas supported by different groups. The data set includes the distribution of 805 species of plants (45 families), mammals (25 families), reptiles (six families), amphibians (five families), birds (18 families), and insects (30 families), and is analysed with the optimality criterion (based on the notion of endemism) implemented in the program NDM/VNDM. Almost 50% of the areas obtained are supported by three or more major groups; areas supported by fewer major groups generally contain species from different genera, families, or orders.© The Willi Hennig Society 2011.

1 November 2015 in Molecular Phylogenetics and Evolution
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Journal Article
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LLLuciana Bolsoni Lourenço
Luciana Bolsoni Lourenço
CTCíntia P. Targueta
Cíntia P. Targueta
DBDiego MICAELA Baldo
Diego MICAELA Baldo
JNJuliana Nascimento
Juliana Nascimento
PGPaulo Garcia
Paulo Garcia
SRShirlei M. Recco-Pimentel
Shirlei M. Recco-Pimentel