Find research datasets worth reusing

Figure 8 in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 8 Number of species and articles authored by Prof. Dr. C. G. Froehlich. A, accumulative curves of the number of publications (red) and species (blue). B, number of publications (red) and species (blue) in periods of five years.

Figure 4 in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 4 The legacy of Prof. Dr. C. G. Froehlich is reflected in several new Brazilian research centers. M.Sc. students (in yellow) and Ph.D. students (in green) advised by him are represented by the initial letters of each name. São Paulo state is magnified. The list of the full name and their respective initials is provide at the Table 2.

Figure 3 in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 3 The foundation of "Froehlich's Autonomous Stonefly Republic". A, Claudio G. Froehlich (CGF), his Ph.D. students Adolfo R. Calor (ARC) and Rodolfo Mariano (RM), and Dr. Eduardo Domínguez (ED) in a collection expedition at the Estação Biológica de Boracéia (EBB/USP), Salesópolis, São Paulo, Brazil, 2007; B, CGF in his classic undergraduate course "Aquatic Entomology" at the EBB/USP, 2005; CGF, his PhD students ARC and RM, and ED in a light trap collect, 2007; CGF and ED in Venerando river, in EBB, collecting stoneflies and mayflies.

Figure 1 in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 1 Prof. Dr. C. G. Froehlich's professional career timeline, with some significant events highlighted in the photographs.

Figure 6 A, The 6 in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 6 A, The 6th International Symposium on Plecoptera, Schlitz, Germany 1977.; B, The 7th International Symposium on Plecoptera, Nara, Japan 1980.

Figure 2 in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 2 Awards received by Prof. Dr. C. G. Froehlich. A, Lifetime Achievement Award, offered by International Association of Plecopterologists, XII International Symposium on Plecoptera, Tucumán, Argentina (1998); B, Plate offered by students and colleagues for the outstanding contribution to Neotropical Aquatic Entomology, 3rd Symposium on Neotropical Aquatic Insects, Ribeirão Preto, Brazil (2015).

Figure 5 A in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 5 A, Prof. Claudio Froehlich at the Museum of Zoology of University of São Paulo (MZUSP) in 1969, São Paulo, Brazil; B, CGF at the 4th International Symposium on Plecoptera, Abisko, Swedish Lapland, 1968; C, CGF and Marlene Sofia Arcifa Froehlich at the XIII International Symposium on Plecoptera, Tafí de Valle, Tucumán, Argentina, August 1998; D, CGF and Oliver Flint, both were honored at the III Symposium on Neotropical Aquatic Insects, Ribeirão Preto, São Paulo, Brazil, 2015; E, CGF in a collection expedition at the Estação Biológica de Boracéia (EBB/USP), Salesópolis, São Paulo, Brazil, 2006.

Figure 7 A, 9 in Not just a taxonomist, but a naturalist! The foundations of "Froehlich's Autonomous Stonefly Republic"

Figure 7 A, 9th International Conference on Ephemeroptera & 13th International Symposium on Plecoptera, Tafí de Valle, Tucumán 16–21 August 1998; B, 15th International Conference on Ephemeroptera & 19 International Symposium on Plecoptera, Aracruz, Brazil 3–8 June 2018.

opencc-zeroJan 2024View details →

Linked collectors and determiners for: Additions and corrections to the type list of Heteroptera (Insecta: Hemiptera) of the Costa Lima Collection, Oswaldo Cruz Foundation.

Natural history specimen data linked to collectors and determiners held within, "Additions and corrections to the type list of Heteroptera (Insecta: Hemiptera) of the Costa Lima Collection, Oswaldo Cruz Foundation". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/b89eef79-c05f-49af-8865-ad714d3cb410">https://bionomia.net/dataset/b89eef79-c05f-49af-8865-ad714d3cb410</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/b89eef79-c05f-49af-8865-ad714d3cb410">https://gbif.org/dataset/b89eef79-c05f-49af-8865-ad714d3cb410</a>. Formatted as a Frictionless Data package.

opencc-zeroJan 2024View details →

Linked collectors and determiners for: SOF herbarium - Swiss Orchid Foundation - Amostras Brasileiras Repatriadas - Herbário Virtual REFLORA.

Natural history specimen data linked to collectors and determiners held within, "SOF herbarium - Swiss Orchid Foundation - Amostras Brasileiras Repatriadas - Herbário Virtual REFLORA". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/9b8ed240-8ecd-443d-8987-f59b53510777">https://bionomia.net/dataset/9b8ed240-8ecd-443d-8987-f59b53510777</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/9b8ed240-8ecd-443d-8987-f59b53510777">https://gbif.org/dataset/9b8ed240-8ecd-443d-8987-f59b53510777</a>. Formatted as a Frictionless Data package.

dryad40/100

Data from: Genetic and functional variation across regional and local scales is associated with climate in a foundational prairie grass

<ul> <li>Global change forecasts in ecosystems require knowledge of within species diversity, particularly of dominant species within communities. We assessed site-level diversity and capacity for adaptation of the dominant species of the shortgrass steppe biome of the Central US, Bouteloua gracilis.</li> <li>We quantified genetic diversity from 17 sites across regional scales, north-south from New Mexico to South Dakota, and local scales in Northern Colorado. We also quantified phenotype and plasticity within and among sites and determined the extent to which phenotypic diversity in B. gracilis was related to climate.</li> <li>Genome sequencing indicated pronounced population structure at the regional scale, and local differences indicated gene flow and/or dispersal may also be limited. Within a common environment, we found evidence for genetic divergence in biomass-related phenotypes, plasticity, and phenotypic variance, indicating functional divergence and different adaptive potential. Phenotypes differentiated according to climate, chiefly median Palmer Hydrological Drought Index and other aridity metrics.</li> <li>Our results indicate conclusive differences in genetic variation, phenotype, and plasticity in this species and suggest a mechanism explaining variation in shortgrass steppe community responses to global change. This analysis of B. gracilis intraspecific diversity across spatial scales will improve conservation and management of the shortgrass steppe ecosystem moving forward.</li> </ul>

opencc-zeroMar 2020View details →

FIGURE 2 in A new morphological dataset reveals a novel relationship for the adzebills of New Zealand (Aptornis) and provides a foundation for total evidence neoavian phylogenetics

FIGURE 2. Majority-rule cladogram of nine most parsimonious trees (length: 2038, CI: 0.2498, RI: 0.5337, RC: 0.1333, HI: 0.7502) from analysis of our new dataset of 40 taxa and 368 osteological characters. All trees show optimization of an Aptornis defossor+Psophia obscura sister group. Synapomorphies are detailed in table 2. Extinct taxa are denoted with daggers. Majority-rule percentages are annotated above branches, followed by bootstrap support values greater than 50% in parentheses. Branch length ranges are below branches.

FIGURE 5 in A new morphological dataset reveals a novel relationship for the adzebills of New Zealand (Aptornis) and provides a foundation for total evidence neoavian phylogenetics

FIGURE 5. Synapomorphies for the pelvis of Aptornis defossor (AMNH 7300, A) and Psophia obscura (AMNH 2671, B). The pelvises are shown in ventral view. Scale bars are different for each specimen and are shown below each specimen. Labels correspond to synapomorphies, with character numbers followed by character states in parentheses. Abbreviations: cio, crista iliaca obliqua; ili, preacetabular ilium; ish, postacetabular ischium; pil, postacetabular ilium; syn, synsacrum

FIGURE 1 in A new morphological dataset reveals a novel relationship for the adzebills of New Zealand (Aptornis) and provides a foundation for total evidence neoavian phylogenetics

FIGURE 1. Strict consensus cladogram of nine most parsimonious trees (length: 2038, CI: 0.2498, RI: 0.5337, RC: 0.1333, HI: 0.7502) from analysis of our new morphological dataset of 40 taxa and 368 characters in PAUP*. Results support optimization of an Aptornis defossor + Psophia obscura sister group. Synapomorphies are detailed in table 2. Extinct taxa are denoted with daggers. Bootstrap support values greater than 50% are annotated above branches, with branch length ranges reported below branches.

FIGURE 3. A in A new morphological dataset reveals a novel relationship for the adzebills of New Zealand (Aptornis) and provides a foundation for total evidence neoavian phylogenetics

FIGURE 3. A. Resulting tree from Bayesian analysis of 32 RAG1 and RAG2 sequences. Clade credibility values greater than 90% are annotated above branches. Core Gruiformes, Ralloidea, and Gruoidea are well supported with 100% clade credibility values. The scale bar at the bottom of the tree denotes branch length. The data were run in MrBayes for 2,000,000 generations.

FIGURE 3 in A new morphological dataset reveals a novel relationship for the adzebills of New Zealand (Aptornis) and provides a foundation for total evidence neoavian phylogenetics

FIGURE 3 (continued). B. Resulting tree from Bayesian analysis of our new dataset of 40 taxa and 368 osteological characters combined with 32 sequences of RAG1 and RAG2 nuclear genes. Clade credibility values greater than 90% are annotated above branches. Extinct taxa are denoted with daggers. The scale bar at the bottom of the tree denotes branch length. The data were run in MrBayes for 1,100,000 generations.

Figure 8 in A redescription of the skull of Euoplocephalus tutus (Archosauria: Ornithischia): a foundation for comparative and systematic studies of ankylosaurian dinosaurs

Figure 8. Rostrum of Euoplocephalus tutus Lambe (1902) in left oblique rostrodorsolateral view. AMNH 5405. Scale bar 70 mm. All abbreviations are listed in Appendix 1.

Figure 16 in A redescription of the skull of Euoplocephalus tutus (Archosauria: Ornithischia): a foundation for comparative and systematic studies of ankylosaurian dinosaurs

Figure 16. Scanning electron micrograph of tooth of Euoplocephalus tutus Lambe (1902). TMP 87.36.99. Scale bar, 10 mm.

Figure 5 in A redescription of the skull of Euoplocephalus tutus (Archosauria: Ornithischia): a foundation for comparative and systematic studies of ankylosaurian dinosaurs

Figure 5. Schematic illustrations of the basicranium of Euoplocephalus tutus Lambe (1902) in right lateral view. (A) Basicranial components of the occipital/basicranial region. (B) Basicranial foramina. Not to scale. Abbreviations in italics (i.e. the frontal and parietal elements) are not considered components of the occipital/basicranial region. All abbreviations are listed in Appendix 1.

Figure 1 in A redescription of the skull of Euoplocephalus tutus (Archosauria: Ornithischia): a foundation for comparative and systematic studies of ankylosaurian dinosaurs

Figure 1. Phylogeny of the Ankylosauria, providing the genealogical context for the taxa discussed in the text (after Vickaryous et al., 2001b). Explanation of nodes: node (1) Ankylosauria; node (2) Nodosauridae; node (3) Ankylosauridae; node (4) Ankylosaurinae. All suprageneric taxonomic nomenclature follows the definitions of Sereno (1998).