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39 results for “Origin of life”

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zenodo40/100

Left: Premaxillary tooth of Stygivenator molnari, from Molnar, 1978, left lateral and posterior views, about twice life size. Right: Lectotype tooth of Aublysodon mirandus, from Leidy, 1860, left lateral and posterior views, slightly smaller than life size. in The origin and evolution of the Tyrannosaurids, Part 1

Left: Premaxillary tooth of Stygivenator molnari, from Molnar, 1978, left lateral and posterior views, about twice life size. Right: Lectotype tooth of Aublysodon mirandus, from Leidy, 1860, left lateral and posterior views, slightly smaller than life size.

opencc-by-4.0Dec 1995View details →
zenodo40/100

Figure 4 A-E in LIFE CYCLE OF NATURAL POPULATIONS OF METRIOCNEMUS (INERMIPUPA) CARMENCITABERTARUM LANGTON & COBO 1997 (DIPTERA: CHIRONOMIDAE) IN THE NETHERLANDS: INDICATIONS FOR A SOUTHERN ORIGIN? Abstract

Figure 4 A-E. Numbers of adults, egg strings and pupal exuviae of Metriocnemus (Inermipupa) carmencitabetarum recorded between April and December in 2012 and 2013 at Appingdam and Nijmegen and of 4th instar larvae at Nijmegen in 2013: 4A number of adults and egg strings at Appingedam, 2012; 4B number of adults and pupal exuviae at Appingedam 2013; 4C number of adults and egg strings at Nijmegen 2012; 4D number of adults and pupal exuviae at Nijmegen 2013; 4E numbers of 4th instar larvae recorded in the upper 50 cm of the water butt at Nijmegen, 2013. Horizontal brackets indicate periods of adult activity of one generation. Periods with no observations are shaded.

opencc-by-4.0Aug 2017View details →
zenodo40/100

Figure 3 in LIFE CYCLE OF NATURAL POPULATIONS OF METRIOCNEMUS (INERMIPUPA) CARMENCITABERTARUM LANGTON & COBO 1997 (DIPTERA: CHIRONOMIDAE) IN THE NETHERLANDS: INDICATIONS FOR A SOUTHERN ORIGIN? Abstract

Figure 3. Emergence pattern of the wintering generation from the Appingedam vase in spring 2014 (black dots and solid line) and hypothetical emergence pattern when larval development would have been interrupted by a diapause (dotted line). Number of pupal exuviae are added up per week.

opencc-by-4.0Aug 2017View details →
zenodo40/100

Figure 5 in LIFE CYCLE OF NATURAL POPULATIONS OF METRIOCNEMUS (INERMIPUPA) CARMENCITABERTARUM LANGTON & COBO 1997 (DIPTERA: CHIRONOMIDAE) IN THE NETHERLANDS: INDICATIONS FOR A SOUTHERN ORIGIN? Abstract

Figure 5. Seasonal length differences in male and female pupal exuviae in Nijmegen in 2013, with a binomial fit (left y-axis). The two wavy lines represent mean weekly minimum and maximum temperatures from April to October (right y-axis).

opencc-by-4.0Aug 2017View details →
zenodo40/100

Figure 1 in LIFE CYCLE OF NATURAL POPULATIONS OF METRIOCNEMUS (INERMIPUPA) CARMENCITABERTARUM LANGTON & COBO 1997 (DIPTERA: CHIRONOMIDAE) IN THE NETHERLANDS: INDICATIONS FOR A SOUTHERN ORIGIN? Abstract

Figure 1. Distribution of Metriocnemus (I.) carmencitabertarum in the Netherlands and the location of the two research sites Appingedam and Nijmegen.

opencc-by-4.0Aug 2017View details →
zenodo40/100

Figure 2 in LIFE CYCLE OF NATURAL POPULATIONS OF METRIOCNEMUS (INERMIPUPA) CARMENCITABERTARUM LANGTON & COBO 1997 (DIPTERA: CHIRONOMIDAE) IN THE NETHERLANDS: INDICATIONS FOR A SOUTHERN ORIGIN? Abstract

Figure 2. Head width and head length of wintering larvae collected in the Appingedam vase in December 2013 and February 2014. Results are projected in a HW-HL graph of the four M. (I.) carmencitabertarum instars obtained from Kuper (2015) revealing wintering in 3rd and 4th larval stage in the Appingedam vase.

opencc-by-4.0Aug 2017View details →
zenodo40/100

Figure 6 in LIFE CYCLE OF NATURAL POPULATIONS OF METRIOCNEMUS (INERMIPUPA) CARMENCITABERTARUM LANGTON & COBO 1997 (DIPTERA: CHIRONOMIDAE) IN THE NETHERLANDS: INDICATIONS FOR A SOUTHERN ORIGIN? Abstract

Figure 6. Correlation between mean ambient temperature during development and skin size for males and females from the Nijmegen water butt in 2013.

opencc-by-4.0Aug 2017View details →
dryad40/100

Juvenile life history, migration, and habitat use of natural- versus hatchery-origin Chinook salmon

Open the record for dataset details and reuse information.

publicMay 2025View details →
zenodo36/100

Identity Lexicon and Keyword Counts for "The Life of a Tie: Social Origins of Network Diversity"

<p>Prototype identity lexicon for the categories of occupation (e.g., "reporter" at Boston Globe), familial roles (e.g., proud "father"), political affiliation (life-long "democrat"), and cultural and sports interests (e.g., "hiphop", "NFL").</p> <p>Also includes a CSV file with counts of each identity keywords matched for all 572K users in our dataset.&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Jun 2024View details →
dryad36/100

Data for: Convergence and contingency in the evolution of a specialized mode of life: Multiple origins and high disparity of rock-boring bivalves

<p>Evolutionary adaptation to novel, specialized modes of life is often associated with close mapping of form to function, resulting in narrow morphological disparity. For Bivalvia, endolithy (rock-boring) has biomechanical requirements thought to diverge strongly from those of the ancestral shallow-burrowing habit in soft sediments. However, 3D morphometric data from 73 species among ~94% of extant endolithic genera and families, along with 384 non-endolithic species in those families, show that endolithy has originated at least eight times. Endolithy is evolutionarily accessible from multiple morphological starting points, evidenced by the morphologies of the oldest fossil members of families. Although some endoliths appear to converge on a limited set of shell morphologies, the total range of endolith shell morphologies among the broadest for bivalve life habits, and lacks any unifying morphological trait. Nevertheless, endolithy is a taxon-poor habit today. This limited richness evidently does not derive from damped origination or heightened extinction rates on lineages containing endoliths, and today's endoliths are not confined to low diversity biogeographic regions. Instead, endolithy may be limited by habitat availability. Both determinism (convergence among distantly related taxa) and contingency (endoliths remain close to the disparate morphologies of their source clades) underlie the occupation of endolith morphospace.</p>

opencc-zeroDec 2022View details →
dryad36/100

The origin of blinking in both mudskippers and tetrapods is linked to life on land

<p>Blinking, the transient occlusion of the eye by one or more membranes, serves several functions including wetting, protecting, and cleaning the eye. This behavior is seen in nearly all living tetrapods and absent in other extant sarcopterygian lineages, suggesting that it might have arisen during the water-to-land transition. Unfortunately, our understanding of the origin of blinking has been limited by a lack of known anatomical correlates of the behavior in the fossil record and a paucity of comparative functional studies. To understand how and why blinking originates, we leverage mudskippers (Oxudercinae), a clade of amphibious fishes that have convergently evolved blinking. Using micro-computed tomography and histology, we analyzed two mudskipper species, <em>Periophthalmus</em> <em>barbarus</em> and <em>Periophthalmodon</em> <em>septemradiatus</em>, and compared them to the fully aquatic round goby, <em>Neogobius</em> <em>melanostomus</em>. Study of gross anatomy and epithelial microstructure shows that mudskippers have not evolved novel musculature or glands to blink. Behavioral analyses show the blinks of mudskippers are functionally convergent with those of tetrapods: <em>P. barbarus</em> blinks more often under high evaporation conditions to wet the eye, a blink reflex protects the eye from physical insult, and a single blink can fully clean the cornea of particulates. Thus, eye retraction in concert with a passive occlusal membrane can achieve functions associated with life on land. Osteological correlates of eye retraction are present in the earliest limbed vertebrates, suggesting blinking capability. In both mudskippers and tetrapods, therefore, the origin of this multifunctional innovation is likely explained by selection for increasingly terrestrial lifestyles.</p>

opencc-zeroMar 2023View details →
dryad36/100

Life Stage, chorion, and hatchery origin differences in the toxicity of 6PPDQ to coho salmon

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publicDec 2025View details →
dryad36/100

Data for: Convergence and contingency in the evolution of a specialized mode of life: Multiple origins and high disparity of rock-boring bivalves

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publicDec 2022View details →
dryad36/100

Adaptive associations among life history, reproductive traits, environment, and origin in the Wisconsin angiosperm flora

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publicApr 2021View details →
dryad36/100

The origin of blinking in both mudskippers and tetrapods is linked to life on land

Open the record for dataset details and reuse information.

publicMar 2023View details →
zenodo32/100

Left: Premaxillary tooth of Stygivenator molnari, from Molnar, 1978, left lateral and posterior views, about twice life size. Right: Lectotype tooth of Aublysodon mirandus, from Leidy, 1860, left lateral and posterior views, slightly smaller than life size. in The origin and evolution of the Tyrannosaurids, Part 1

Left: Premaxillary tooth of Stygivenator molnari, from Molnar, 1978, left lateral and posterior views, about twice life size. Right: Lectotype tooth of Aublysodon mirandus, from Leidy, 1860, left lateral and posterior views, slightly smaller than life size.

opennotspecifiedDec 1995View details →
zenodo32/100

Left: Premaxillary tooth of Stygivenator molnari, from Molnar, 1978, left lateral and posterior views, about twice life size. Right: Lectotype tooth of Aublysodon mirandus, from Leidy, 1860, left lateral and posterior views, slightly smaller than life size. in The origin and evolution of the Tyrannosaurids, Part 1

Left: Premaxillary tooth of Stygivenator molnari, from Molnar, 1978, left lateral and posterior views, about twice life size. Right: Lectotype tooth of Aublysodon mirandus, from Leidy, 1860, left lateral and posterior views, slightly smaller than life size.

opennotspecifiedDec 1995View details →
dryad32/100

Data from: Reconstructing the origins of high-alpine niches and cushion life form in the genus Androsace s.l. (Primulaceae)

Relatively few species have been able to colonize extremely cold alpine environments. We investigate the role played by the cushion life form in the evolution of climatic niches in the plant genus Androsace s.l., which spreads across the mountain ranges of the Northern Hemisphere. Using robust methods that account for phylogenetic uncertainty, intraspecific variability of climatic requirements and different life history evolution scenarios, we show that climatic niches of Androsace s.l. exhibit low phylogenetic signal and that they evolved relatively recently and punctually. Models of niche evolution fitted onto phylogenies show that the cushion life form has been a key innovation providing the opportunity to occupy extremely cold environments, thus contributing to rapid climatic niche diversification in the genus Androsace. We then propose a plausible scenario for the adaptation of plants to alpine habitats.

opencc-zeroDec 2010View details →
ClinicalTrials.gov32/100

Effect of VSL#3 (Original De Simone Formulation) on Cognitive Function, Risk of Falls and Quality of Life in Patients With Cirrhosis

ClinicalTrials.gov study NCT01686698. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data from: Reconstructing the origins of high-alpine niches and cushion life form in the genus Androsace s.l. (Primulaceae)

Open the record for dataset details and reuse information.

publicApr 2013View details →

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Allen Brain Atlas

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allen-brain-atlas
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Annotated Behaviour and Observability Dataset (ABODe)

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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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record