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 “Magpie”
MAgPIE model runs outputs: Climate change-driven global land-use system adaptation under CMIP6-based crop model projections
<p>Each folder contains the fulldata.gdx and the configuration files for each MAgPIE run based on the nine crop impact models and 5 gcms used in the paper.</p>
Data from: Great spotted cuckoo nestlings have no antipredatory effect on magpie or carrion crow host nests in southern Spain
Host defences against cuckoo parasitism and cuckoo trickeries to overcome them are a classic example of antagonistic coevolution. Recently it has been reported that this relationship may turn to be mutualistic in the case of the carrion crow (Corvus corone) and its brood parasite, the great spotted cuckoo (Clamator glandarius), given that experimentally and naturally parasitized nests were depredated at a lower rate than non-parasitized nests. This result was interpreted as a consequence of the antipredatory properties of a fetid cloacal secretion produced by cuckoo nestlings, which presumably deters predators from parasitized host nests. This potential defensive mechanism would therefore explain the detected higher fledgling success of parasitized nests during breeding seasons with high predation risk. Here, in a different study population, we explored the expected benefits in terms of reduced nest predation in naturally and experimentally parasitized nests of two different host species, carrion crows and magpies (Pica pica). During the incubation phase non-parasitized nests were depredated more frequently than parasitized nests. However, during the nestling phase, parasitized nests were not depredated at a lower rate than non-parasitized nests, neither in magpie nor in carrion crow nests, and experimental translocation of great spotted cuckoo hatchlings did not reveal causal effects between parasitism state and predation rate of host nests. Therefore, our results do not fit expectations and, thus, do not support the fascinating possibility that great spotted cuckoo nestlings could have an antipredatory effect for host nestlings, at least in our study area. We also discuss different possibilities that may conciliate these with previous results, but also several alternative explanations, including the lack of generalizability of the previously documented mutualistic association.
Figure 3 in Variability of daily nest survival and breeding success in relation to characteristics of Eurasian magpie (Pica pica) nests
Figure 3. Relationships between nest diameter and breeding success in magpie breeding population in central Iran.
Figure 2 in Variability of daily nest survival and breeding success in relation to characteristics of Eurasian magpie (Pica pica) nests
Figure 2. Relationships between nest height and breeding success in magpie breeding population in central Iran.
Figure 1 in Variability of daily nest survival and breeding success in relation to characteristics of Eurasian magpie (Pica pica) nests
Figure 1. Relationships between nest height and fledging success in magpie breeding population in central Iran.
Data from: Great spotted cuckoo nestlings have no antipredatory effect on magpie or carrion crow host nests in southern Spain
Open the record for dataset details and reuse information.
Data from: Host nest site choice depends on risk of cuckoo parasitism in magpie hosts
Open the record for dataset details and reuse information.
Data from: Helper effects in the azure-winged magpie Cyanopica cyana in relation to highly-clumped nesting pattern and high frequency of conspecific nest-raiding
Open the record for dataset details and reuse information.
Data from: Telomere dynamics in parasitic great spotted cuckoos and their magpie hosts
Open the record for dataset details and reuse information.
Data from: Decoding colouration of begging traits by the experimental addition of the appetite enhancer cyproheptadine hydrochloride in magpie (Pica pica) nestlings
Open the record for dataset details and reuse information.
Data from: Heritability of plumage colour morph variation in a wild population of promiscuous, long-lived Australian magpies
Open the record for dataset details and reuse information.
Data from: Cognitive performance is linked to group size and affects fitness in Australian magpies
Open the record for dataset details and reuse information.
Brood parasitism, provisioning rates and breeding phenology of male and female magpie hosts
<p class="CuerpoA"><span>Parental care is a costly behaviour that raises the prospects of offspring survival. In species with biparental care these costs are shared by both parents, although there may be a conflict regarding the relative investment of each sex. Avian brood parasites leave all the costs of rearing offspring to their hosts. The magnitude of these costs and their consequences on the relative role of both sexes in parental care and future reproduction remain mostly unknown. Here, we investigate whether provisioning rate of nestlings by magpie hosts (<i>Pica pica</i>) differs between broods parasitized by the great spotted cuckoo (<i>Clamator glandarius</i>) and non-parasitized broods, and whether the relative contribution of each sex to provisioning is affected by parasitism. Furthermore, we explore the effect of parasitism on magpie's future reproduction. We found that provisioning rate was similar in parasitized and non-parasitized broods, and that the relative contribution of males and females was also similar, irrespectively of the parasitism status. However, rearing parasitic offspring seems to have a negative long-term effect on magpie's breeding phenology in the following breeding season. Our results suggest that, although brood parasitism by great spotted cuckoos does not seem to influence the relative contribution of both sexes to parental care, it may entail long-term extra costs in terms of breeding delay for magpies.</span></p>
Data from: High level of extrapair fertilizations in individual Tibetan azure-winged magpies and their adaptive responses
Extrapair fertilizations (EPFs) occur widely in socially monogamous birds and result in mixed parentage in the brood. The response of an individual to these EPFs of its social mate remains poorly investigated in terms of parental care for the mixed brood. We addressed this question in a cooperatively-breeding corvid, the azure-winged magpie Cyanopica cyana. Parentage analysis indicated that 45% of females and 37% of males engaged in EPFs. There were 49% of cooperative groups and 36% of bi-parental nests with extrapair paternity (EPP) offspring, and 22% of cooperative groups and 19% of bi-parental nests with extrapair maternity (EPM) offspring. Based on the identity of offspring, we classified adults into four types: EPP offspring fathers/mothers, EPM offspring fathers/mothers, cuckolded males/females, and faithful males/females. A comparison of provisioning rates among all four types of breeders showed that 1) EPM offspring fathers had the highest provisioning rate; 2) cuckolded males did not reduce parental care, compared to faithful males and EPP offspring fathers; and 3) females of different types did not differ in their provisioning rates. Our findings suggest that a combination of frequent opportunities, low costs of cuckoldry, and the benefits of establishing a cooperative neighbourhood can explain why EPFs occur frequently in the Tibetan population of azure-winged magpie.
Data from: Great spotted cuckoo disregard information on conspecific breeding success while parasitizing magpie
The study of mechanisms underlying host selection by brood parasites usually lays on selection by parasites of host traits that inform on host parental abilities or location. However, brood parasites might use information extracted from past reproductive performance of either their hosts or themselves, a possibility almost neglected. In this study, we use a long-term data set to analyse whether the probability of parasitism by great spotted cuckoos (Clamator glandarius) of a magpie (Pica pica) nest in a given year is related with the reproductive outcome of any of the two species in the surroundings of that nest the previous year. We found that probability of parasitism for a nest in a year was explained by previous year cuckoo reproductive outcome and parasitism rate in the area surrounding the focal nest, but not by host reproductive outcome. To discern between the effect of parasitism rate and that of parasite reproductive success on parasite choices we carried out an experiment modifying the natural correlation found between parasitism status and host and parasite success in the patches. The results showed that neither host nor cuckoo reproductive outcome in a patch after the experiment explained probability of parasitism the following year. Only parasitism rate in the surroundings of a nest before the experiment explained probability of parasitism for this nest in the following year. Hence, these results indicate that great spotted cuckoos disregard social information related to past parasitism outcome, probably because parasitism outcome is tightly correlated with parasitism itself.
Example data for MAgPIE workshop
Open the record for dataset details and reuse information.
MAgPIE model input data sets: Climate change-driven global land-use system adaptation under CMIP6-based crop model projections
<p>These MAgPIE input data sets include harmonized crop yield projections from several crop models (9 crop models and 5 climate models). Additionally, regional, validation, and calibration data sets are also reported.</p>
Fig. 10 in Introgression at the emerging secondary contact zone of magpie Pica pica subspecies (Aves: Corvidae): integrating data on nuclear and mitochondrial markers, vocalizations, and field observations
Fig. 10 Spectrograms of chatter calls of pure P. p. leucoptera, pure P. p. jankowskii, and hybrids. a leucoptera, pair #4, Choibalsan, eastern Mongolia. b jankowskii, pair #6, Vladivostok, Russian Far East. c, d Bilingual hybrid, the same bird from the pair #24, Kerulen, eastern Mongolia. e Hybrid with mixed call, pair #39, Kerulen. f Presumably hybrid with mixed call, pair #5, Kerulen. X-axis—time in s; Y-axis—frequency in kHz
Fig. 8 in Introgression at the emerging secondary contact zone of magpie Pica pica subspecies (Aves: Corvidae): integrating data on nuclear and mitochondrial markers, vocalizations, and field observations
Fig. 8 Genetic structure of the contact zone and its vicinities by mtDNA and SNPs. Above—distribution of haplotypes of mitochondrial CR along conditional population numbers I–VI depicted in Fig. 3. Green—western haplotype; red—eastern haplotype. Below— graphical representation of individual contributions from nuclear
Fig. 3 in Introgression at the emerging secondary contact zone of magpie Pica pica subspecies (Aves: Corvidae): integrating data on nuclear and mitochondrial markers, vocalizations, and field observations
Fig. 3 Map of sampling localities for nuclear SNP analysis. Distribution of genotypes of nuclear SNPs revealed by ddRAD analysis are shown with blue circles for Pica pica leucoptera and red circles for Pica pica jankowskii. Bi-colored circles mean mixed (hybrid) genotype: portion of blue/red corresponds to probability of it belonging to one of the groups, as revealed in the Structure analysis. Numbers
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.