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123 results for “Trait correlation”

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zenodo44/100

Dataset of Proportion of non-native plants in urban parks correlates with climate, socioeconomic factors and plant traits

<p>Full datasets for the research entitled &#39;Proportion of non-native plants in urban parks correlates with climate, socioeconomic factors and plant traits&#39;.</p>

opencc-by-4.0Sep 2020View details →
edi44/100

Stachewicz et al. 2021: Trait correlation, phylogenetic signal in Carabidae morphology (repackaging of occurrences published by the NEON Biorepository Data Portal)

Stachewicz JD, Fountain-Jones NM, Koontz A, Woolf H, Pearse WD, Gallinat AS. 2021. Strong trait correlation and phylogenetic signal in North American ground beetle (Carabidae) morphology bioRxiv 02.12.431029; doi: https://doi.org/10.1101/2021.02.12.431029 Many NEON samples and specimens used in this work resulted from NEON prototype data and will not be archived in the Biorepository. See the appendices in the above linked article for a full list of NEON samples and specimens and their associated collection data. Additionally, see appendices of above linked article for specimen-level morphological trait measurements and genetic sequence data.

openCC0Feb 2023View details →
dryad40/100

Maternal and genetic correlations between morphology and physical performance traits in a small captive primate, Microcebus murinus

<p>Physical performance traits are key components of fitness and direct targets of selection. Maternal effects are important components of integrated phenotypes in a variety of species. Yet their contribution to variation in performance, and phenotypes closely associated with performance, remains poorly understood. We used an animal model approach to quantify the contribution of maternal effects to performance trait variation (in bite force and pull strength) and the relationships between performance and the relevant underlying morphology in <i>Microcebus murinus</i>. We show that bite force is heritable (h<sup>2</sup>~0.23), and that maternal effects are also important source of variation, resulting in a medium inclusive heritability (IH<sup>2</sup>~0.47). Grip strength presented a rather low and non-significant narrow-sense heritability suggesting a higher selective pressure on this trait. Genetic correlations between performance traits and their associated morphometric traits were significant and high (0.47 bite force-head width; 0.48 grip strength-radius length), as was the maternal correlation for bite force-head width (0.75). Further studies evaluating the heritability of performance for other taxa and the role of maternal effects are badly needed to better understand the drivers of variation in performance ultimately allowing for a better understanding of the importance of these types of traits in an evolutionary context.</p>

opencc-zeroDec 2020View details →
dryad40/100

Maternal and genetic correlations between morphology and physical performance traits in a small captive primate, Microcebus murinus

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publicFeb 2022View details →
dryad36/100

Data from: Correlated evolution between climate and suites of traits along a fast-slow continuum in the radiation of Protea

Evolutionary radiations are responsible for much of Earth's diversity, yet the causes of these radiations are often elusive. Determining the relative roles of adaptation and geographic isolation in diversification is vital to understanding the causes of any radiation, and whether a radiation may be labeled as 'adaptive' or not. Across many groups of plants, trait-climate relationships suggest that traits are an important indicator of how plants adapt to different climates. In particular, analyses of plant functional traits in global databases suggest that there is an "economics spectrum" along which combinations of functional traits covary along a fast-slow continuum. We examine evolutionary associations among traits and between trait and climate variables on a strongly supported phylogeny in the iconic plant genus Protea to identify correlated evolution of functional traits and the climatic-niches that species occupy. Results indicate that trait diversification in Protea has climate associations along two axes of variation: correlated evolution of plant size with temperature and leaf investment with rainfall. Evidence suggests that traits and climatic-niches evolve in similar ways, although some of these associations are inconsistent with global patterns on a broader phylogenetic scale. When combined with previous experimental work suggesting that trait-climate associations are adaptive in Protea, the results presented here suggest that trait diversification in this radiation is adaptive.

opencc-zeroDec 2017View details →
dryad36/100

Data from: Functional traits and community composition: a comparison among community-weighted means, weighted correlations, and multilevel models

1. Of the several approaches that are used to analyze functional trait-environment relationships, the most popular is community-weighted mean regressions (CWMr) in which species trait values are averaged at the site level and then regressed against environmental variables. Other approaches include model-based methods and weighted correlations of different metrics of trait-environment associations, the best known of which is the fourth-corner correlation method. 2. We investigated these three general statistical approaches for trait-environment associations: CWMr, five weighted correlation metrics (Peres-Neto et al. 2017), and two multilevel models (MLM) using four different methods for computing p-values. We first compared the methods applied to a plant community dataset. To determine the validity of the statistical conclusions, we then performed a simulation study. 3. CWMr gave highly significant associations for both traits, while the other methods gave a mix of support. CWMr had inflated type I errors for some simulation scenarios, implying that the significant results for the data could be spurious. The weighted correlation methods had generally good type I error control but had low power. One of the multilevel models, that from Jamil et al. (2013), had both good type I error control and high power when an appropriate method was used to obtain p-values. In particular, if there was no correlation among species in their abundances among sites, a parametric bootstrap likelihood ratio test (LRT) gave the best power. When there was correlation among species in their abundances, a conditional parametric LRT had correct type I errors but had lower power. 4. There is no overall best method for identifying trait-environment associations. For the simple task of testing, one-by-one, associations between single environmental variables and single traits, the weighted correlations with permutation tests all had good type I error control, and their ease of implementation is an advantage. For the more complex task of multivariate analyses and model fitting, and when high statistical power is needed, we recommend MLM2 (Jamil et al. 2013); however, care must be taken to ensure against inflated type I errors. Because CWMr exhibited highly inflated type I error rates, it should always be avoided. 2. We investigated these three general statistical approaches for trait-environment associations: CWMr, five weighted correlation metrics (Peres-Neto et al. 2017), and two multilevel models (MLM) using five different methods for computing p-values. We first compared the methods applied to a plant community dataset. To determine the validity of the statistical conclusions, we then performed a simulation study. 3. CWMr gave highly significant associations for both traits, while the other methods gave a mix of support. CWMr had inflated type I errors for some simulation scenarios. The weighted correlation methods had generally good type I error control but had low power. One of the multilevel models, that from Jamil et al. (2013), had both good type I error control and high power when an appropriate method was used to obtain p-values. In particular, if there was no correlation among species in their abundances among sites, a parametric bootstrap likelihood ratio test (LRT) gave the best power. When there was correlation among species in their abundances, a conditional parametric LRT had correct type I errors but suffered from low power. 4. There is no overall best method for identifying trait-environment associations. For the simple task of testing, one-by-one, associations between single environmental variables and single traits, the weighted correlations with permutation tests all had good type I error control, and their ease of implementation is an advantage. For the more complex task of multivariate analyses and model fitting, and when high statistical power is needed, we recommend MLM2 (Jamil et al. 2013); however, care must be taken to ensure against inflated type I errors. Because CWMr exhibited highly inflated type I error rates, it should be avoided.

opencc-zeroDec 2017View details →
dryad36/100

Data from: Artificial selection on sexual aggression: correlated traits and possible trade‐offs

<p>Forced copulation is an extreme form of sexual aggression that can affect the evolution of sex-specific anatomy, morphology and behavior. To characterize mechanistic and evolutionary aspects of forced copulation, we artificially selected male fruit flies based on their ability to succeed in the naturally prevalent behavior of forced matings with newly eclosed (teneral) females. The low and high forced copulation lineages showed rapid divergence, with the high lineages ultimately showing twice the rates of forced copulation as the low lineages. While males from the high lineages spent more time aggressively pursuing and mounting teneral females, their behavior towards non-teneral and heterospecific females was similar to that of males from the low lineages. Males from the low and high lineages also showed similar levels of male-male aggression. This suggests little or no genetic correlations between sexual aggression and non-aggressive pursuit of females, and between male aggression towards females and males. Surprisingly however, males from the high lineages had twice as high mating success than males from the low lineages when allowed to compete for consensual mating with mature females. In further experiments, we found no evidence for trade-offs associated with high forced mating rates: males from the high lineages did not have lower longevity than males from the low lineages when housed with females, and four generations of relaxed selection did not lead to convergence in forced mating rates. Our data indicate complex interactions among forced copulation success and consensual mating behaviour, which we hope to clarify in future genomic work. </p>

opencc-zeroMay 2020View details →
dryad36/100

Correlation between fine root traits and pathogen richness depends on plant mycorrhizal types

<p class="MsoNormal"><span><span>Root uptake strategies are associated with the strength of negative plant</span><span>–</span><span>soil feedback induced (PSF) induced by soil pathogens. Given the intensified effect of pathogen richness in fine roots on the strength of negative PSF through the synergistic effects of multiple pathogens, researchers have proposed a trade-off between nutrient acquisition and pathogen defence in roots. However, empirical evidence is lacking. In addition, because the interaction between pathogens and fine roots depends on the mycorrhizal types of tree species, both fine root traits and mycorrhizal types should be incorporated to reveal covariation in pathogen richness and the strength of negative PSF. In this study, we selected 50 arbuscular mycorrhizal (AM) tree species and 7 ectomycorrhizal (ECM) tree species in a subtropical forest to investigate the relationships between fine root traits and pathogen richness in fine roots and determined whether their relationships depended on plant mycorrhizal types. Our results showed that pathogen richness was negatively correlated with fine root diameter but was positively correlated with specific root length for the AM-associated species, while for the ECM-associated species, the pathogen richness was only found to have a significant negative relationship with the relative abundance of ECM fungi. These findings highlight the difference between AM- and ECM-associated species in pathogen defence and bridge the gap between root traits and pathogen richness, which is significant for improving our understanding of the potential factors mediating the strength of PSF and thus maintaining tree species diversity.</span></span></p>

opencc-zeroOct 2022View details →
dryad36/100

Data from: A comparative study of body size evolution in moths: Evidence of correlated evolution with feeding and phenology-related traits

<p>Interspecific variation in body size is one of the most popular topics in comparative studies. Despite recent advances, little is still known about the patterns and processes behind the evolution of body size in insects. Here, we used a robust data set comprising all geometrid moth species occurring in Northern Europe to examine the evolutionary associations involving body size and several life-history traits under an explicitly phylogenetic framework. We provided new insights into the interactive effects of life-history traits on body size and evidence of correlated evolution. We further established the sequence of trait evolution linking body size with the life-history traits correlated with it. We found that most (but not all) of the studied life-history traits, to some extent, interfered with interspecific variation in body size, but interactive effects were uncommon. Both bi- and multivariate phylogenetic analyses indicated that larger species tend to be nocturnal flyers, overwinter in the larval stage, feed on the foliage of trees rather than herbs, and have a generalist feeding behavior. We found evidence of correlated evolution involving body size with overwintering stage, host-plant growth form, and dietary specialization. The examination of evolutionary transitions within the correlated models signaled that overwintering as larvae preceded the evolution of large sizes, as did feeding on tree foliage and the generalist feeding behavior. By showing that both body size and all life-history traits correlated with it evolve at very slow rates, we caution against uncritical attempts to propose causal explanations for respective associations based on contemporary ecological settings.</p>

opencc-zeroMay 2024View details →
zenodo36/100

Result of LAVA-Knock: Genetic correlation via knockoffs removes confounding due to cross-trait assortative mating

<p>Results of application to GWAS summary statistics for 36 traits. 394,060 windows are used to perform LAVA-Bonf. 64,833 windows are used to conduct LAVA-Knock. At target FDR 0.1, LAVA-Knock detects 8,421 significant windows for 4,401 locus-phenotype pairs. LAVA-Bonf with threshold 0.05/394,060 identifies 10,802 windows for 6,260 locus-phenotype pairs.</p>

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

Data for: Strong phenotypic trait correlations between mating partners do not result from assortative mating in wild great tits (Parus major)

<p>There is considerable debate about the occurrence of assortative mating between phenotypic traits measured within natural populations. Meta-analyses have implied that assortative mating occurs generally in natural populations but recent work indicates these conclusions largely result from biased data. Specifically, estimates of phenotypic correlations between mating partners do not solely result from non-random associations between individual-level traits of partners but also from other biological processes (joint phenotypic plasticity, indirect genetic effects), methodological practices (observer bias), and other unexplained residual correlations (e.g. correlated measurement error). This paper puts this critique to test. First, we estimated the overall phenotypic correlation between phenotypic traits of mating partners for a wild population of great tits. Second, we estimated various key variance components to reveal the extent to which phenotypic correlations between partners resulted from assortative mating, reversible plasticity, social partner effects, and methodological practices. We performed our analyses for a range of phenotypic traits (body mass, breathing rate, exploration behaviour, wing and tarsus length) to derive general conclusions not hinging on the specifics of the traits involved. Our analyses support the conclusion that patterns of assortative mating exist at first glance but occur because of the biasing effects of correlated residuals likely caused by a combination of phenotypic responses to unknown environmental factors or measurement error – not because of intrinsic patterns of assortative mating.</p>

opencc-zeroSep 2021View details →
dryad36/100

Data for: Phylogenetically controlled life history trait meta-analysis in cetaceans reveals unexpected negative brain size and longevity correlation

<p>The identification of patterns in trait evolution is essential to understand the interaction of evolutionary forces, and provides useful information for species management. Cetaceans are a phylogenetically well-resolved infraorder that exhibit distinct trait variation across behavioural, molecular and life history dimensions, yet few researchers have applied a meta-analytic or comparative approach to these traits. To understand cetacean trait evolution, we used a phylogenetic generalised least squares approach to examine the cognitive buffer hypothesis (CBH). A large brain should buffer individuals against environmental challenges through increasing survival rates, and a longer lifespan should buffer individuals against the cost of extended development for larger brains according to the CBH, leading to an expected positive correlation between brain size and lifespan. In contrast to this expectation, previously observed in taxa including primates, we found a negative correlation between brain size and lifespan in cetaceans. This suggests cetaceans experience selective pressures different from most other mammals in these traits but may be more similar to some social mammalian carnivores that display alloparenting. We also provide a comprehensive dataset to explore additional aspects of trait evolution but which would greatly benefit from studies on behavioural ecology across cetaceans and increased focus on data-deficient species. </p>

opencc-zeroFeb 2023View details →
dryad36/100

Data for: Strong phenotypic trait correlations between mating partners do not result from assortative mating in wild great tits (Parus major)

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publicSep 2021View details →
dryad36/100

Data from: Functional traits and community composition: a comparison among community-weighted means, weighted correlations, and multilevel models

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publicNov 2018View details →
dryad36/100

Data from: Heritability and correlations among learning and inhibitory control traits

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publicMar 2020View details →
dryad36/100

Simulating contests to determine the relative importance of correlated traits on the winning chances

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publicSep 2025View details →
dryad36/100

An ecological-evolutionary investigation of phenotypic, genetic, and environmental variation and correlations among reproductive traits of tall goldenrod (<em>Solidago altissima</em>)

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publicJan 2026View details →
dryad36/100

Data from: Correlated evolution of male and female reproductive traits drive a cascading effect of reinforcement in Drosophila yakuba

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publicJun 2016View details →
dryad36/100

Data from: Artificial selection on sexual aggression: correlated traits and possible trade‐offs

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publicMay 2020View details →
dryad36/100

Data from: Correlated evolution between climate and suites of traits along a fast-slow continuum in the radiation of Protea

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publicDec 2018View details →

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dandi-nwb
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International Brain Laboratory public data

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Last verified 2026-04-29Open record