Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
43
datasets available to search
ShareScore release 0.9.0
Dataset results
43 results for “Correa”
Supplementary material 1 from: von Tschirnhaus J, Correa C (2021) The definitive rediscovery of Telmatobius halli (Anura, Telmatobiidae) at its historic type locality and its synonymy with T. dankoi and T. vilamensis. ZooKeys 1079: 1-33. https://doi.org/10.3897/zookeys.1079.69036
Video S1. Warm springs swimming bath at source of Río Loa in Chile, 1935.
Figure 6 from: von Tschirnhaus J, Correa C (2021) The definitive rediscovery of Telmatobius halli (Anura, Telmatobiidae) at its historic type locality and its synonymy with T. dankoi and T. vilamensis. ZooKeys 1079: 1-33. https://doi.org/10.3897/zookeys.1079.69036
Figure 6 Adults from the three known populations of Telmatobius halli, as recognized in this study, showing the similarity in their external appearance A Miño B Las Cascadas and C Vilama River. The inlay in the upper right corner of C shows a detail of the keratinous spines. Photograph credits for the Vilama River specimen: Felipe Rabanal. Scale bars: 1 cm.
Figure 5 from: von Tschirnhaus J, Correa C (2021) The definitive rediscovery of Telmatobius halli (Anura, Telmatobiidae) at its historic type locality and its synonymy with T. dankoi and T. vilamensis. ZooKeys 1079: 1-33. https://doi.org/10.3897/zookeys.1079.69036
Figure 5 Selected specimens of Telmatobius halli from Miño A–D dorsal views of adult specimens, showing variation in coloration patterns E ventral view of the specimen from C F tadpole; scale bar: 1 cm (A–F).
Figure 3 from: von Tschirnhaus J, Correa C (2021) The definitive rediscovery of Telmatobius halli (Anura, Telmatobiidae) at its historic type locality and its synonymy with T. dankoi and T. vilamensis. ZooKeys 1079: 1-33. https://doi.org/10.3897/zookeys.1079.69036
Figure 3 Historic and current view of the concrete swimming pool in Miño A panorama extracted from video footage from the IHAEC, 1935. Yellow arrows indicate the upper and lower pool walls B same view in 2020.
Figure 2 from: von Tschirnhaus J, Correa C (2021) The definitive rediscovery of Telmatobius halli (Anura, Telmatobiidae) at its historic type locality and its synonymy with T. dankoi and T. vilamensis. ZooKeys 1079: 1-33. https://doi.org/10.3897/zookeys.1079.69036
Figure 2 Historic and current panoramic view of the area surrounding the concrete swimming pool in Miño A panorama extracted from video footage from the IHAEC, 1935. Yellow arrows indicate rock formations that are easily recognizable B current state of the habitat. Red rectangle = location of the concrete pool. The mountain in the left background is Miño Volcano.
Figure 7 from: von Tschirnhaus J, Correa C (2021) The definitive rediscovery of Telmatobius halli (Anura, Telmatobiidae) at its historic type locality and its synonymy with T. dankoi and T. vilamensis. ZooKeys 1079: 1-33. https://doi.org/10.3897/zookeys.1079.69036
Figure 7 Bayesian consensus tree (50% majority-rule; mitochondrial genes concatenated, treated as two separated partitions), showing the relationships among Chilean Telmatobius and the species groups recovered by Sáez et al. (2014). The specimens of the species and populations of the extreme south of the distribution of the genus in Chile are highlighted with the same colors of the map in Fig. 1A. The values next to the nodes correspond to posterior probabilities and the scale bar below the tree represents the expected substitutions per site along the branches. Identification of populations of Copaquire, Quebrada Chiclla, Quebrada Choja, and Aguas Calientes follows the taxonomy prior to Fibla et al. (2018) and Cuevas et al. (2020). The red box indicates the taxonomic changes proposed in this study.
Figure 2 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 2 Adult males of Alsodes from the new discovered localities. In parentheses the specific identification according to the phylogenetic analysis (Fig. 3), the snout-vent length (SVL) and code of the respective buccal mucosa sample are indicated. A. Vegas de Cisternas (A. hugoi, SVL = 68.3 mm, VC1m). B. Cajón de Plaza (undetermined, SVL = 54.8 mm, CP5m). C. Vegas de Andrade (A. hugoi, SVL = 57.2 mm, VA1m). D. Vegas de Miranda (A. hugoi, SVL = 56.3 mm, VM6m). E. Cajón Lagunitas (site 3) (A. hugoi, SVL = 71.7 mm, CLP3-5m). F. Lo Aguirre Chico (A. pehuenche, SVL = 52.0 mm, AgCh4m). Some populations are characterized by well-developed interdigital webbing in the hind feet (shown in the insets).
Figure 1 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 1 New and literature records of Alsodes from the Andes Range between 34°50' and 38°05'S. Yellow circles represent the new localities reported in this study; squares represent type localities. A. Andean localities of Alsodes of the literature between 34°50' and 38°05'S: the southernmost localities of A. montanus and A. tumultuosus, the type locality of A. hugoi, localities of A. pehuenche (within red box B, see map B) and the type locality of A. vittatus. There is a record of a putative new species related to A. nodosus in Pemehue (Alsodes sp. 1 of Blotto et al. 2013; not included in the map), presumably the same type locality of A. vittatus. Red boxes correspond to the three explored areas described in this study (maps B, C and D). B. Area explored during the first field campaign (Paso Pehuenche, Laguna del Maule and surroundings). All colored symbols correspond to localities of A. pehuenche: yellow circles correspond to new records; green circles and the square are all previously known localities of the species. The white circle is the place where no amphibian was found. C. Area and sites explored during the third field campaign (tributaries of the Guaiquivilo River). D. Area and sites explored during the second field campaign (surroundings of Laguna El Dial). See details of the localities and the populations discovered in Table 1. Orange lines represent the boundary between Chile and Argentina; thinner yellow lines indicate the boundaries of the administrative regions of Chile.
Figure 3 from: Correa C, Zepeda P, Lagos N, Salinas H, Palma RE, Vásquez D (2018) New populations of two threatened species of Alsodes (Anura, Alsodidae) reveal the scarce biogeographic knowledge of the genus in the Andes of central Chile. Zoosystematics and Evolution 94(2): 349-358. https://doi.org/10.3897/zse.94.25189
Figure 3 Bayesian consensus tree (50% majority-rule) showing the relationships of the new Andean populations of Alsodes. Representatives of the new populations are labeled in green (related to A. pehuenche) and red (related to A. hugoi) (see details of the new localities in Table 1). Note that specimens from Cajón de Plaza are distributed in both the red and green clades. Reference sequences of the type localities of A. pehuenche and A. hugoi are in bold. Numbers next to the nodes correspond to posterior probabilities (only values ≥ 0.95 of the more internal nodes are shown). The scale bar in the lower left corner represents the expected substitutions per site along the branches.
Figure 6 from: Correa C, Durán F (2019) Taxonomy, systematics and geographic distribution of ground frogs (Alsodidae, Eupsophus): a comprehensive synthesis of the last six decades of research. ZooKeys 863: 107-152. https://doi.org/10.3897/zookeys.863.35484
Figure 6 Consensus phylogram (50% mayority-rule) of the Bayesian analysis of the mitochondrial fragments cytochrome c oxidase subunit I and cytochrome b. For simplicity, the outgroup (Alsodesnorae) is not shown. Colored branches indicate the specimens of the two putative species: Villarrica (green) and Tolhuaca (red). The values next to the nodes are the posterior probabilities (pp); asterisks represent maximum values (pp = 1). Note that all species currently recognized (Suárez-Villota et al. 2018b) are supported by high pp values (> 0.97), except for both of the vertebralis group, wich are not reciprocally monophyletic. The scale bar under the tree represents the expected substitutions per site.
Figure 4 from: Correa C, Durán F (2019) Taxonomy, systematics and geographic distribution of ground frogs (Alsodidae, Eupsophus): a comprehensive synthesis of the last six decades of research. ZooKeys 863: 107-152. https://doi.org/10.3897/zookeys.863.35484
Figure 4 Cryptic coloration and variation of coloration patterns in two undetermined populations of the Eupsophusroseus group A adult females from Pidenco, showing cryptic coloration resembling the forest ground; insets show head profiles of the same individuals B adults and juveniles from Las Lianas exemplifying variation in coloration patterns. Both localities were included as Eupsophus sp. in the map of Fig. 3.
Figure 5 from: Correa C, Durán F (2019) Taxonomy, systematics and geographic distribution of ground frogs (Alsodidae, Eupsophus): a comprehensive synthesis of the last six decades of research. ZooKeys 863: 107-152. https://doi.org/10.3897/zookeys.863.35484
Figure 5 Examples of intrapopulation external variation in adult specimens of the type localities of two species of the Eupsophusroseus group AEupsophusroseus from Valdivia BEupsophusmigueli from Mehuín. Both examples illustrate the variation in dorsal and ventral (B) coloration, iris color and snout shape.
Figure 1 from: Correa C, Durán F (2019) Taxonomy, systematics and geographic distribution of ground frogs (Alsodidae, Eupsophus): a comprehensive synthesis of the last six decades of research. ZooKeys 863: 107-152. https://doi.org/10.3897/zookeys.863.35484
Figure 1 Composition of the genus Eupsophus between 1961 and 2018 according to several reviews and studies. Year of species description is provided in parentheses. Capurro (1958) and Cei (1958, 1960, 1962a, 1962b) recognized the same two species of Grandison (1961), but with different names (see comment in Cei 1962b). †Revalidated by Formas and Vera (1982) (removed from the synonymy of E.roseus). ‡Undescribed species from Isla Wellington (Chile), sister to E.calcaratus. §It appears as Eupsophus sp. 1 in Blotto et al. (2013). |Probable undescribed species from Tolhuaca (Chile), sister to E.roseus. ¶Putative species from Villarrica (Chile), sister to E.roseus.
Figure 3 from: Correa C, Durán F (2019) Taxonomy, systematics and geographic distribution of ground frogs (Alsodidae, Eupsophus): a comprehensive synthesis of the last six decades of research. ZooKeys 863: 107-152. https://doi.org/10.3897/zookeys.863.35484
Figure 3 Compilation of localities of Eupsophus species gathered from the literature (see the complete list of localities in Appendix 1). Multicolored circles and the star indicate localities where two or three species of the same group have been reported in the same or different sources. White circles indicate the localities where two undescribed species have been identified (Villarrica and Tolhuaca), two undetermined populations included in this study (Fig. 4) and several ones considered by Correa et al. (2017) as E.roseus, whose taxonomic status is uncertain according to the current taxonomy (Suárez-Villota et al. 2018b). Thin gray lines within Chile represent boundaries of Administrative Regions.
Figure 2 from: Correa C, Durán F (2019) Taxonomy, systematics and geographic distribution of ground frogs (Alsodidae, Eupsophus): a comprehensive synthesis of the last six decades of research. ZooKeys 863: 107-152. https://doi.org/10.3897/zookeys.863.35484
Figure 2 Phylogenetic hypotheses of Eupsophus obtained with DNA sequences. In some of these studies several phylogenetic analyses were made but here we show the hypotheses preferred by the authors. The trees were simplified by merging the terminal nodes by species or other relevant groupings and uniforming the branch lengths, but maintaining the original topologies. The numbers next to the nodes indicate the bootstrap or jackknife support values for the maximum parsimony (MP) analyses or posterior probability for those of Bayesian inference (BI). Black circles over the nodes indicate maximum support. The number of specimens included for each taxon or population is indicated in parentheses (omitted when only one was included). When relevant, the localities of origin of some specimens are indicated in parentheses. For simplicity, some names were abbreviated (for example, Esep = E.septentrionalis; Esp = Eupsophus sp.). Below the trees are indicated the gene fragments used, whether they are mitochondrial (mt) or nuclear (nuc), the analysis strategy (concatenated: ctd; species tree: st) and the phylogenetic reconstruction method used. ANuñez (2003); this is the only tree of those shown where morphological characters (15) were included to build it BNuñez et al. (2011); the only one of these studies where not all species of the genus were included; lineages A-F were considered a priori as E.calcaratusCBlotto et al. (2013); the alternative position of E.septentrionalis (with its respective support value) obtained with a Bayesian analysis of the same data set is shown in red; the method used was MP with direct optimization (do); the support values correspond to jackknife absolute frequencies DCorrea et al. (2017); note that several undescribed populations (Eupsophus sp. = Esp) appear intermixed with some nominal species of the roseus group; in this analysis E.contulmoensis (Econ) and E.nahuelbutensis (Enah) make up a clade but they are not reciprocally monophyletic ESuárez-Villota et al. (2018a); in this analysis E.vertebralis (Ever) and E.emiliopugini (Eemi) are not reciprocally monophyletic FSuárez-Villota et al. (2018b); they obtained a different topology within the roseus group in maximum likelihood and BI analyses of the same concatenated data set (not shown).
Figure 1 from: Correa C (2021) A solution to the enigma of the type locality of Telmatobius halli Noble, 1938 (Anura, Telmatobiidae), a frog lost for 86 years. ZooKeys 1060: 183-192. https://doi.org/10.3897/zookeys.1060.67904
Figure 1 Upper area of the Loa River and surroundings, showing the location of populations recently assigned to Telmatobius halli, its type locality according to this study and other Telmatobius populations near Ollagüe. The railway line that connected Ollagüe with the Collahuasi mine (to the Montt station) and the dirt road that connected the Collahuasi mine and Chiclla with Miño (white arrows) are indicated. Note that the road continues from Miño to the Carcote salt flat. The background map was constructed by joining two maps published by the Comisión Chilena de Límites in 1912.
Supplementary material 1 from: Arias T, Chaux-Varela J, Camero MP, Calderón-Álvarez RA, Trujillo AC, Correa-Munera MA, Zuluaga A, Perdomo O, Pérez-Escobar OA, Trujillo-Trujillo E, Valencia-D. J (2023) Checklist of Orchidaceae from Caquetá, Colombia. PhytoKeys 229: 21-46. https://doi.org/10.3897/phytokeys.229.102737
Supplementary data
Figure 5 from: Vargas-Fonseca S, Correa-Carmona Y, Montes-Rodríguez JM, Calero-Mejía H, Zilli A (2020) Synopsis of fruit-piercing moths of the genus Eudocima (Lepidoptera, Erebidae) from Colombia. ZooKeys 953: 85-104. https://doi.org/10.3897/zookeys.953.50709
Figure 5 Records of Eudocima moths in the city of Bogotá, annual distribution vs precipitation.
Figure 1 from: Vargas-Fonseca S, Correa-Carmona Y, Montes-Rodríguez JM, Calero-Mejía H, Zilli A (2020) Synopsis of fruit-piercing moths of the genus Eudocima (Lepidoptera, Erebidae) from Colombia. ZooKeys 953: 85-104. https://doi.org/10.3897/zookeys.953.50709
Figure 1 Distribution of Eudocima fruit-piercing moths in Colombia.
Figure 2 from: Blanco-Gutiérrez I, Esteve P, Garrido A, Gómez-Ramos A, Arce A, Zubelzu S, Díaz-Ambrona CH, Sánchez R, Calatrava J, López-Correa JM (2021) RECLAMO: Unlocking the potential of wastewater reuse for agricultural irrigation in Spain . Research Ideas and Outcomes 7: e76793. https://doi.org/10.3897/rio.7.e76793
Figure 2 GANNT Diagram.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.