Skip to main content
Powered by ShareScore

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.

37

datasets available to search

ShareScore release 0.9.0

Reset

Dataset results

37 results for “complex life cycles”

Learn how ShareScore rates datasets ↗
dryad32/100

Data from: The trophic vacuum and the evolution of complex life cycles in trophically-transmitted helminths

Open the record for dataset details and reuse information.

publicAug 2014View details →
dryad32/100

Data from: Affinity, life cycle, and intracellular complexity of organic-walled 2 microfossils from the Mesoproterozoic of Shanxi, China

Open the record for dataset details and reuse information.

publicFeb 2015View details →
dryad32/100

Integrating top-down and bottom-up effects of local density across scales and a complex life cycle

Open the record for dataset details and reuse information.

publicApr 2023View details →
dryad28/100

Data from: More than meets the eye: detecting cryptic microgeographic population structure in a parasite with a complex life cycle

Nonrandom recruitment of parasites among hosts can lead to genetic differentiation among hosts and mating dynamics that promote inbreeding. It has been hypothesized that strictly aquatic parasites with intermediate hosts will behave as panmictic populations among hosts because ample opportunity exists for random mixing of unrelated individuals during transmission to the definitive host. A previous allozyme study on the marine trematode Lecithochirium fusiforme did not support this hypothesis in that there was genetic differentiation among, and significant heterozygote deficiencies within, definitive hosts. We revisit this system and use microsatellites to obtain multilocus genotypes. Our goal was to determine if cryptic subgroups and/or the presence of clones could account for the apparent deviation from 'panmixia'. We find strong evidence for cryptic subdivision (three genetic clusters) that causes the Wahlund effect and differentiation among definitive hosts. After accounting for these cryptic groups, we see panmictic genetic structure among definitive hosts that is consistent with the "high mixing in aquatic habitats" hypothesis. We see evidence for co-transmission of clones in all three clusters, but this level of clonal structure did not have a major impact in causing deviations from Hardy-Weinberg equilibrium, and only affected genetic differentiation among hosts in one cluster. A cursory examination of the data may have led to incorrect conclusions about non-random transmission. However, it is obvious in this system that there is more than meets the eye in relation to the actual makeup of parasite populations. In general, the methods we employ will be useful for elucidating hidden patterns in other organisms where cryptic structure may be common (e.g., those with limited morphology or complex life histories).

opencc-zeroDec 2010View details →
dryad28/100

Data from: Effects of complex life cycles on genetic diversity: cyclical parthenogenesis

Neutral patterns of population genetic diversity in species with complex life cycles are difficult to anticipate. Cyclical parthenogenesis (CP), in which organisms undergo several rounds of clonal reproduction followed by a sexual event, is one such life cycle. Many species, including crop pests (aphids), human parasites (trematodes) or models used in evolutionary science (Daphnia), are cyclical parthenogens. It is therefore crucial to understand the impact of such a life cycle on neutral genetic diversity. In this paper, we describe distributions of genetic diversity under conditions of CP with various clonal phase lengths. Using a Markov chain model of CP for a single locus and individual-based simulations for two loci, our analysis first demonstrates that strong departures from full sexuality are observed after only a few generations of clonality. The convergence towards predictions made under conditions of full clonality during the clonal phase depends on the balance between mutations and genetic drift. Second, the sexual event of CP usually resets the genetic diversity at a single locus towards predictions made under full sexuality. However, this single recombination event is insufficient to reshuffle gametic phases towards full-sexuality predictions. Finally, for similar levels of clonality, CP and acyclic partial clonality (wherein a fixed proportion of individuals are clonally produced within each generation) differentially affect the distribution of genetic diversity. Overall, this work provides solid predictions of neutral genetic diversity that may serve as a null model in detecting the action of common evolutionary or demographic processes in cyclical parthenogens (for example, selection or bottlenecks).

opencc-zeroDec 2015View details →
dryad28/100

Data from: Evolutionary consequence of a change in life cycle complexity: a link between precocious development and evolution towards female-biased sex allocation in a hermaphroditic parasite

The evolutionary consequences of changes in the complex life cycles of parasites are not limited to the traits that directly affect transmission. For instance, mating systems that are altered due to precocious sexual maturation in what is typically regarded as an intermediate host may impact opportunities for outcrossing. In turn, reproductive traits may evolve to optimize sex allocation. Here we test the hypothesis that sex allocation evolved towards a more female-biased function in populations of the hermaphroditic digenean trematode Alloglossidium progeneticum that can precociously reproduce in their second hosts. In these precocious populations, parasites are forced to self-fertilize as they remain encysted in their second hosts. In contrast, parasites in obligate 3-host populations have more opportunities to outcross in their third host. We found strong support that in populations with precocious development, allocation to male resources was greatly reduced. We also identified a potential phenotypically plastic response in a body size-sex allocation relationship that may be driven by the competition for mates. These results emphasize how changes in life cycle patterns that alter mating systems can impact the evolution of reproductive traits in parasites.

opencc-zeroDec 2014View details →
zenodo28/100

Figure 3 in Parallelism in secondary loss of sex from a heterogonic life cycle on different host plants in the Andricus mukaigawae complex (Hymenoptera: Cynipidae), with taxonomic notes

Figure 3. The life cycles, gall shape of unisexual generation, and suggested changes in the Andricus mukaigawae complex.

opencc-by-4.0Mar 2007View details →
dryad28/100

Data from: Complex life cycles: why refrain from growth before reproduction in the adult niche?

Open the record for dataset details and reuse information.

publicAug 2012View details →
dryad28/100

Data from: More than meets the eye: detecting cryptic microgeographic population structure in a parasite with a complex life cycle

Open the record for dataset details and reuse information.

publicMar 2011View details →
dryad28/100

Data from: Genotypic and phenotypic variation in transmission traits of a complex life cycle parasite

Open the record for dataset details and reuse information.

publicJun 2013View details →
dryad28/100

Data from: Evolutionary consequence of a change in life cycle complexity: a link between precocious development and evolution towards female-biased sex allocation in a hermaphroditic parasite

Open the record for dataset details and reuse information.

publicOct 2015View details →
dryad28/100

Data from: Effects of complex life cycles on genetic diversity: cyclical parthenogenesis

Open the record for dataset details and reuse information.

publicJun 2016View details →
dryad24/100

Data from: Exploitation of the same trophic link favors convergence of larval life-history strategies in complex life cycle helminths

Switching from one host to the next is a critical life history transition in parasites with complex life cycles. Growth and mortality rates are thought to influence the optimal time and size at transmission, but these rates are difficult to measure in parasites. The parasite life cycle, in particular the trophic link along which transmission occurs, may be a reasonable proxy for these rates, leading to the hypothesis that life cycle should shape life history strategy. We compiled data on the size and age at infectivity for trophically-transmitted helminths (i.e. acanthocephalans, cestodes, and nematodes), and then categorized species into trophic links (e.g. planktonic crustaceans to fish, insects to terrestrial vertebrates, etc.). Comparative analyses that explicitly included stabilizing selection within trophic links fit the data significantly better than random walk models, indicating that parasites with different life cycles have different optimal times/sizes for host switching. The major helminth groups have often independently evolved similar life cycles, and we show that this has frequently led to convergent and/or parallel evolution of size and age at infectivity. This suggests that for particular life cycles there are universal optimal transmission strategies, applicable to widely divergent taxa, although the cases of parallelism might indicate that lineage-specific constraints sometimes prevent evolution to a single adaptive peak.

opencc-zeroDec 2010View details →
dryad24/100

Data from: Mechanisms of biotic resistance across complex life cycles

1. Biotic resistance is the ability of communities to inhibit the establishment, spread or impact of novel species. However, the interactions that underlie biotic resistance depend heavily on the contexts in which species interact. Consequently, studies of biotic resistance that consider single processes, patches, species or life-history stages may provide an incomplete picture of the capacity for communities to resist invasion. 2. Many organisms have multiphasic life cycles, where individuals can occupy distinct niches at different stages of the life-history. Generally, studies of biotic resistance focus on interactions within a single life-history stage, and interactions at other life-history stages are overlooked. Here, we demonstrate that different mechanisms of biotic resistance occur across the life history and together limit the invasion success of an introduced marine invertebrate (Ciona intestinalis) in northern California. 3. We tested the role of interactions (competition and predation) with the resident community in limiting the abundance of Ciona through experiments conducted on fertilization, larval survival, settlement, early post-settlement survival, and the survival of juveniles and adults. 4. Under some circumstances, Ciona became abundant in mid-successional stages and showed more rapid growth rates than a morphologically similar native species, Ascidia ceratodes. However, predators reduced Ciona abundance much more than that of Ascidia at several life stages. 5. Furthermore, Ciona appeared to be a weaker competitor at the adult stage. Early life-history interactions with other sessile species at the fertilization, larval and recruit stages had modest to no effects on Ciona abundance. 6. The presence of biotic resistance mechanisms acting at multiple life stages, and potentially under different conditions, suggests that different components of biotic resistance interact to enhance the resident community's resistance to invasion.

opencc-zeroDec 2012View details →
dryad24/100

Data from: Mechanisms of biotic resistance across complex life cycles

Open the record for dataset details and reuse information.

publicAug 2013View details →
dryad24/100

Data from: Exploitation of the same trophic link favors convergence of larval life-history strategies in complex life cycle helminths

Open the record for dataset details and reuse information.

publicMar 2011View details →
geo24/100

The role of gene duplication in shaping divergent patterns of gene expression across a complex life cycle

GEO Series GSE253389. Danaus plexippus. 50 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJan 2024View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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