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.
87
datasets available to search
ShareScore release 0.9.0
Dataset results
87 results for “Animal evolution”
Figure 3 in Early animal Two hypotheses for the early radiation of the metazoans are evolution: a morphologist 's view.
Figure 3. Early animal evolution according to the Ctenophora hypothesis (based on losses)ı with an indication of losses of important characters. Losses are in blue.
Figure 1. Notobryon wardi Odhner, 1936. Living animals. A in Molecular data illuminate cryptic nudibranch species: the evolution of the Scyllaeidae (Nudibranchia: Dendronotina) with a revision of Notobryon
Figure 1. Notobryon wardi Odhner, 1936. Living animals. A, Australia, New South Wales, Port Stephens, photo by Ron Greer; B, Philippines, Luzon Island, Batangas Province, Anilao, Photo by T. M. Gosliner, CASIZ 177589; C, Philippines, Luzon Island, Batangas Province, Calumpan Peninsula, photo by T. M. Gosliner, CASIZ 177537; D, Marshall Islands, Kwajalein Atoll, South Loi Island, photo by J. Johnson, CASIZ 180378; E, Papua New Guinea, North coast, near Madang, photo by T. M. Gosliner, CASIZ 075283; F, Notobryon sp.B, Philippines, Luzon Island, Batangas Province, Anilao, Mainit Bubbles, photo by T. M. Gosliner, CASIZ 177759.
Data from: Why are animals conspicuously colored? Evolution of sexual versus warning signals in land vertebrates
Open the record for dataset details and reuse information.
Data from: Plasticity of animal genome architecture unmasked by rapid evolution of a pelagic tunicate
Open the record for dataset details and reuse information.
Data from: Individual cryptic scaling relationships and the evolution of animal form
Open the record for dataset details and reuse information.
Data from: Evolution of diet across the animal Tree of Life
Open the record for dataset details and reuse information.
Data from: Convergent evolution of cytochrome P450s underlies independent origins of keto-carotenoid pigmentation in animals
Open the record for dataset details and reuse information.
Data from: Climatic-niche evolution follows similar rules in plants and animals
Open the record for dataset details and reuse information.
Animation of MS evolution in young star clusters
<p>The video shows the evolution of binary and single stellar models from 1Myr to 100Myr. </p>
Data from: Convergence of ion channel genome content in early animal evolution
Multicellularity has evolved multiple times, but animals are the only multicellular lineage with nervous systems. This fact implies that the origin of nervous systems was an unlikely event, yet recent comparisons among extant taxa suggest that animal nervous systems may have evolved multiple times independently. Here, we use ancestral gene content reconstruction to track the timing of gene family expansions for the major families of ion-channel proteins that drive nervous system function. We find that animals with nervous systems have broadly similar complements of ion-channel types but that these complements likely evolved independently. We also find that ion-channel gene family evolution has included large loss events, two of which were immediately followed by rounds of duplication. Ctenophores, cnidarians, and bilaterians underwent independent bouts of gene expansion in channel families involved in synaptic transmission and action potential shaping. We suggest that expansions of these family types may represent a genomic signature of expanding nervous system complexity. Ancestral nodes in which nervous systems are currently hypothesized to have originated did not experience large expansions, making it difficult to distinguish among competing hypotheses of nervous system origins and suggesting that the origin of nerves was not attended by an immediate burst of complexity. Rather, the evolution of nervous system complexity appears to resemble a slow fuse in stem animals followed by many independent bouts of gene gain and loss.
Datasets of Fornoni et al. FREQUENCY DEPENDENT SELECTION AND THE EVOLUTION OF RECIPROCAL EXPLOITATION IN PLANT-ANIMAL INTERACTIONS.
<p>Datasets and RMarkdown</p> <p><span lang="EN-GB">Paper title: FREQUENCY DEPENDENT SELECTION AND THE EVOLUTION OF RECIPROCAL EXPLOITATION IN PLANT-ANIMAL INTERACTIONS.</span></p> <p><span lang="EN-GB">Authors: </span><span lang="ES-MX">Juan Fornoni, </span><span lang="EN-GB">Sergio Ramos, Roberto Alvarez-Martínez, Carlos Cordero, </span><span lang="EN-GB">and César A. Domínguez</span></p>
Figure 1 from: Vinarski M (2015) Conceptual shifts in animal systematics as reflected in the taxonomic history of a common aquatic snail species (Lymnaea stagnalis). Zoosystematics and Evolution 91(2): 91-103. https://doi.org/10.3897/zse.91.4509
Figure 1 - A great pond snail in its natural environment. 12.08.2014. Russia, Western Siberia, "Malaya Sos'va" Nature Reserve, Kopanoye Lake (photo: M. Vinarski).
Figure 4 from: Vinarski M (2015) Conceptual shifts in animal systematics as reflected in the taxonomic history of a common aquatic snail species (Lymnaea stagnalis). Zoosystematics and Evolution 91(2): 91-103. https://doi.org/10.3897/zse.91.4509
Figure 4 - Varieties of Lymnaea stagnalis as they were identified by malacologists of the 19th century. A. Lymnaea stagnalis var. typica (det. S. Clessin; ZIN). B. Lymnaea stagnalis var. media (det. C.A. Westerlund; GNM). C. Lymnaea stagnalis var. producta (det. C.A. Westerlund; GNM). D. Lymnaea stagnalis var. rosea (identified by a unknown person; ZMUC). E. Lymnaea stagnalis var. colpodia (det. C.A. Westerlund; GNM). F. Lymnaea stagnalis var. variegata (det. C.A. Westerlund; GNM). G. Lymnaea stagnalis var. turgida (det. C.A. Westerlund; GNM). H. Lymnaea stagnalis var. raphidia (det. C.A. Westerlund; GNM). I. Lymnaea stagnalis var. palustriformis (det. A. Fuchs, NHMW). Scale bars 5 mm.
Figure 2 from: Vinarski M (2015) Conceptual shifts in animal systematics as reflected in the taxonomic history of a common aquatic snail species (Lymnaea stagnalis). Zoosystematics and Evolution 91(2): 91-103. https://doi.org/10.3897/zse.91.4509
Figure 2 - Evolution of accuracy in illustrations of Lymnaea stagnalis shell through two centuries. Sources of images: A. Aldrovandi 1606. B. Lister 1678. C. Bonanni 1681. D. Klein 1753. E. Seba 1758. F. Schröter 1779.
Figure 4 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 4 - Stenothoe bartholomea sp. n. female 3 mm holotype. P 3–4, P 6–7 peraeopod 3–4; peraeopod 6–7; P 4', P 4'' entire leg with coxa resp. distal end of propodus P 4 enlarged; P 7' distal end of propodus P 7 enlarged.
Figure 7 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 7 - Stenothoe miersii (Haswell, 1879) male 3 mm; P 5–7 peraeopod 5–7; U 1–3 uropod 1–3; U 3' third uropod enlarged; Ep 3 third epimeral plate; T telson.
Figure 3 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 3 - Stenothoe bartholomea sp. n. female 3 mm holotype. Gn 2, Gn 2', Gn 2'' gnathopod 2 from both sides and tip of carpus + merus resp. palmar corner enlarged.
Figure 19 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 19 - Stenula solsbergi (Schneider, 1884): Md mandible; Mx 1 maxilla 1; Gn 1 gnathopod 1; Gn 1', Gn 1 '' gnathopod 1 right and left distally enlarged.
Figure 18 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 18 - Stenula pugilla sp. n. male 3 mm: Gn 2 gnathopod 2; P 6, 7 peraeopod 6, 7; U 1–3 uropod 1–3; T telson.
Figure 15 from: Krapp-Schickel T, Vader W (2015) Stenothoids living with or on other animals (Crustacea, Amphipoda). Zoosystematics and Evolution 91(2): 215-246. https://doi.org/10.3897/zse.91.5715
Figure 15 - Stenula pugilla sp. n. female 3 mm: Gn 1 gnathopod 1 distal arts; Gn 2 gnathopod 2; Gn 2' gnathopod 2 distally enlarged.
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.