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430 results for “Reproductive success”
Fig. 2 in Spatio-Temporal Structure And Reproductive Success In A Rook (Corvus Frugilegus) Colony
Fig. 2. Relationship between the date of nesting and the elapsed time from nesting to egg laying. Spearman rank correlation: r s = –0.695, n = 102, P <0.01
Fig. 1 in Spatio-Temporal Structure And Reproductive Success In A Rook (Corvus Frugilegus) Colony
Fig. 1. Temporal distribution of nest building and egg laying. Bars represent the number of nests that were started to build (white) and number of nests in which the first egg was laid (grey) grouped into five-day periods. n = 20, mean±SD: 40.00±5.94 and 76.33±8.80 days, respectively
Fig. 4 in Spatio-Temporal Structure And Reproductive Success In A Rook (Corvus Frugilegus) Colony
Fig. 4. Distance of the newly built nests from the centre of the colony, from the edge of the colony (metres) and number of neighbouring nests within 6 metres (medians, full circles) and those of the randomly selected points (medians, empty squares) at each sampling date. 100 random points were selected for each date, sample sizes of the observed nests are shown above the medians. In the marked (*) cases the values of the observed nests dif- fered significantly from the values of the ran- dom points (Mann-Whitney test, P <0.05)
Position in the laying order has sex-specific consequences for reproductive success in adult black-headed gulls
<p><span>Mothers who produce multiple offspring within one reproductive attempt often allocate resources differentially; some maternally-derived substances are preferentially allocated to last-produced offspring and others to first-produced offspring. The combined effect of these different allocation regimes on the overall fitness of offspring produced early or late in the sequence is not well understood, partly because production order is often coupled with birth order, making it difficult to separate effects of pre-natal maternal allocation from those of post-natal social environments. In addition, very little is known about the influence of laying order on fitness in later-life. In this study, we used a semi-natural captive colony of black-headed gulls to test whether an offspring's position in the laying order affected its early life survival and later life reproductive success, independent of its hatching order. Later-laid eggs were less likely to hatch, but among those that did, survival to adulthood was greater than that of first-laid eggs. In adulthood, the laying order of females did not affect their likelihood of breeding in the colony, but male offspring hatched from last-laid eggs were significantly less likely to gain a breeding position than earlier-laid males. In contrast, later-laid female parents hatched lower proportions of their clutches than first-laid females, but hatching success was unrelated to the laying order of male parents. Our results indicate that gull mothers induce complex and sex-specific effects on both the early survival of their offspring and on long-term reproductive success through laying order effects among eggs of the same breeding attempt.<strong> </strong></span></p>
Data from Investigating the effects of diurnal and nocturnal pollinators on male and female reproductive success and on floral trait selection in Silene dioica
<p><strong>data_all_OdEx.csv</strong>: all data about phenotypes or reproductive success at the individual scale</p> <ul> <li>ID : ID name</li> <li>nGrSemis_min : seed number needed to be sowned to get enough seedlings</li> <li>nGrGerm : seed number effectively sowned</li> <li>nGrGerm_OK : number of germinated seed</li> <li>TauxGerm : germination rate</li> <li>nFruits_MAX : maximal number of fruit that the plant could have produced</li> <li>nFruits_OK : effective number of fruits that the plant had produced</li> <li>nFruits_OK_avecPred : effective number of fruits that the plant had produced ignoring predation</li> <li>nFruits_pred : number of predated fruits</li> <li>mean_nbSeeds : mean number of seeds per fruit</li> <li>sd_nbSeeds : sd number of seeds per fruit</li> <li>mean_nbOv : mean ovule non fertilize per fruit</li> <li>sd_nbOv : sd ovule non fertilize per fruit</li> <li>mean_nbOvTOT : mean ovule number per flower</li> <li>sd_nbOvTOT : sd ovule number per flower</li> <li>prodTOT : total number of seed produced including germination rate</li> <li>FS : Fruit-set</li> <li>SS : Seed-set</li> <li>prodTOTsg : total number of seed produced without germination rate</li> <li>nbFlo_run0 : flower number at the beginning of the experiment</li> <li>nbFlo_run1 : flower number at the first measurement</li> <li>mean_nbFlo : mean flower number</li> <li>MeanFec : mean seed sired per males according to MEMM model</li> <li>MeanDelta : mean delta pollen dispersion according to MEMM model</li> <li>MeanMRS : mean male reproductive success (including female RS) according to MEMM model</li> <li>MedFec : same as above with the median</li> <li>MedDelta : same as above with the median</li> <li>MedMRS : same as above with the median</li> <li>VarFec : same as above with the variance</li> <li>VarDelta : same as above with the variance</li> <li>VarMRS : same as above with the variance</li> <li>ciFec : Same as above with confidence interval</li> <li>ciDelta : Same as above with confidence interval</li> <li>ciMRS : Same as above with confidence interval</li> <li>MS_Res : mating success</li> <li>mean_lFl : mean corolla width</li> <li>mean_hFl : mean calyx height</li> <li>QttTOT : pollen number per flower</li> <li>pop : which originate population</li> <li>cohort : which cohort</li> </ul> <p><strong>data_seeds_OdEx.csv</strong> : all data about seed number of weight as well as unfertilized ovule at the fruit scale for female RS</p> <ul> <li>ID : ID name</li> <li>noFruit : ID fruit</li> <li>poids : seed weight</li> <li>nbSeeds : number of seeds</li> <li>nbOv : number of unfertilized ovule</li> <li>moySeeds : mean seed size</li> <li>varSeeds : variance in seed size</li> </ul> <p><strong>data_poll_OdEx.csv</strong> : all data about pollinator observation session</p> <ul> <li>ID : ID name</li> <li>session : observation session number</li> <li>nbVis : number of independent insect attracted</li> <li>nbVisTot : number of total visit</li> <li>binVis : individual visited or not</li> </ul>
Fig. 2 in Spatial Variation In Prey Composition And Its Possible Effect On Reproductive Success In An Expanding Eastern Imperial Eagle (Aquila Heliaca) Population
Fig. 2. Cluster analyses of imperial eagle breeding areas based on prey composition data. Region codes are presented in Fig. 1. Codes with bold characters represent mountainous habitats. The single breeding pair of the Cserehát Mountains was excluded from the analysis, because of low sample size
Fig. 3 in Spatial Variation In Prey Composition And Its Possible Effect On Reproductive Success In An Expanding Eastern Imperial Eagle (Aquila Heliaca) Population
Fig. 3. Frequency of the three main prey species (a-c) and reproductive success (d) of imperial eagles in two East-Hungarian regions. Boxplots presents the minimum-maximum (whiskers), lower and upper quartiles (box) and the median (line) of the data. Dots are outliers. Significance of difference is in-
Figure 1 in Successful reproduction of dragonflies in an artistic water fountain in Versailles, France
Figure 1. Artistic fountain in the Palace of Versailles, Paris, a breeding habitat for Aeshna cyanea and Sympetrum striolatum.
One for all and all for one: phenotype assortment and reproductive success in masculinized females
<p>Homophily by morphological and behavioral traits has been described in several species of vertebrates, but its functional consequences remain poorly studied. Homophily by plurally breeding females may improve direct fitness by enhancing reproductive success. Female mammals may exhibit phenotypical masculinization due to exposure to androgens during early development, a condition that is associated with maternal performance during subsequent breeding. Our goal was to assess whether female composition (in terms of masculinization) of plurally breeding groups influences female fitness in a natural population of degus <i>(Octodon degus).</i> We assessed if plurally breeding female degus assort themselves by anogenital distance (AGD), an accurate measure of masculinization level. We also quantified if homophily by AGD phenotype affects female reproductive success and the reproductive output of the group. Plurally breeding groups typically included similarly masculinized (i.e., long AGD) females or similarly feminized (short AGD) females, indicating a strong degree of homophily. Females weaned more offspring in plurally breeding groups with more masculinized females. Additionally, standardized variance in the number of offspring weaned decreased in plurally breeding groups with mostly masculinized females, indicating greater reproductive equality in these groups. We conclude that female degus organize into homophilic social groups of similar AGD, and that social groups of masculinized females exhibit higher reproductive success.</p>
Fig. 1 in Reproductive success and female preference in the amazonian cichlid angel fish, Pterophyllum scalare (Lichtenstein, 1823)
Fig. 1. Survival of the eggs in relation to the aggressiveness of experienced males (Pearson, p <0.01).
Fig. 2 in Reproductive success and female preference in the amazonian cichlid angel fish, Pterophyllum scalare (Lichtenstein, 1823)
Fig. 2. Survival of the eggs in relation to care provided by experienced males through aeration (Pearson, p <0.01).
Data for: The association between personalities, alternative breeding strategies, and reproductive success in dunnocks
<p>Although consistent between-individual differences in behaviour (i.e. animal personality) are ubiquitous in natural populations, relatively few studies have examined how personalities influence the formation of social relationships. Yet, behavioural characteristics of both sexes might be key when it comes to pair-bond formation, and the cooperation with partners to successfully rear offspring. We here use a wild population of dunnocks (<i>Prunella modularis</i>) to first investigate whether individuals mate non-randomly (i.e. assortative mating) with regard to four behavioural traits – flight-initiation distance (FID), provisioning, activity, and vigilance – that differ in repeatability and have previously been associated with mating patterns and fitness in other species. Second, we test whether an individual's FID is associated with variability in the dunnocks' mating system (i.e. monogamous pairs vs. polygamous groups). Finally, we determine whether FID and provisioning of males and females associate with their reproductive success. We found no statistical support for assortative mating in FID between males and females. Interestingly, in polygamous groups, co-breeding males differed in their FIDs with dominant alpha-males having significantly shorter FIDs compared to subordinate beta-males. Moreover, there was evidence for assortative mating in provisioning for alpha-males and females in polygamous groups. We also found that male provisioning influenced reproductive success of both sexes, while female provisioning rates only positively correlated with her own but not their partner(s) reproductive output. Our results suggest that personality differences may have important implications for social relationships, the emergence of different mating patterns and ultimately reproductive success within populations.</p>
Data from: Tall, heterogenous forests improve prey capture, delivery to nestlings, and reproductive success for Spotted Owls in southern California
<p>Predator-prey interactions can be profoundly influenced by vegetation conditions, particularly when predator and prey prefer different habitats. Although such interactions have proven challenging to study for small and cryptic predators, recent methodological advances substantially improve opportunities for understanding how vegetation influences prey acquisition and strengthen conservation planning for this group. The California Spotted Owl (<em>Strix</em> <em>occidentalis</em> <em>occidentalis</em>) is well-known as an old-forest species of conservation concern, but whose primary prey in many regions – woodrats (<em>Neotoma</em> spp.) – occurs in a broad range of vegetation conditions. Here, we used high-resolution GPS tracking coupled with nest video monitoring to test the hypothesis that prey capture rates vary as a function of vegetation structure and heterogeneity, with emergent, reproductive consequences for Spotted Owls in Southern California. Foraging owls were more successful capturing prey, including woodrats, in taller multilayered forests, in areas with higher heterogeneity in vegetation types, and near forest-chaparral edges. Consistent with these findings, Spotted Owls delivered prey items more frequently to nests in territories with greater heterogeneity in vegetation types and delivered prey biomass at a higher rate in territories with more forest-chaparral edge. Spotted Owls had higher reproductive success in territories with higher mean canopy cover, taller trees, and more shrubby vegetation. Collectively, our results provide additional and compelling evidence that a mosaic of large tree forests with complex canopy and shrubby vegetation increases access to prey with potential reproductive benefits to Spotted Owls in landscapes where woodrats are a primary prey item. We suggest that forest management activities that enhance forest structure and vegetation heterogeneity could help curb declining Spotted Owl populations while promoting resilient ecosystems in some regions.</p>
Data from: Reproductive senescence and mating tactic interact and conflict to drive reproductive success in a passerine
<p>An understanding of the drivers of individual fitness is a fundamental component of evolutionary ecology and life-history theory. Reproductive senescence, mate and mating tactic choice, and latent heterogeneity in individual quality interact to affect individual fitness. We sought to disentangle the effects of these fitness drivers, where longitudinal data are required to understand their respective impacts. We used reproductive allocation and success data from a long-term (1989-2018) study of white-throated dippers (Cinclus cinclus) in Switzerland to simultaneously examine the effects of female and male age, mating tactic, nest initiation date, and individual heterogeneity on reproductive performance. We modeled quadratic and categorical effects of age on reproductive parameters. The probability of polygyny increased with age in both sexes before declining in older age classes. Similarly, hatching probability in monogamous pairs and the number of nestlings hatched in both monogamous and polygynous pairs increased with female age before declining later in life. As predicted, offspring survival in monogamous pairs increased with male age before declining in older age classes, but male age had no effect on offspring survival in polygynous nesting attempts. Our results demonstrate that parental age, mating tactic, and individual heterogeneity all affect reproductive success, and that the impacts of senescent decline are expressed across different demographic components as a function of sex-specific senescent decline and mating tactic.</p>
Pre-fertilisation gamete thermal environment influences reproductive success, unmasking opposing sex-specific responses in Atlantic Salmon
<p>The environment gametes perform in just before fertilisation is increasingly recognised to affect offspring fitness, yet the contributions of male and female gametes and their adaptive significance remain largely unexplored. Here, we investigated gametic thermal plasticity and its effects on hatching success and embryo performance in Atlantic salmon (Salmo salar). Eggs and sperm were incubated overnight at 2°C or 8°C, temperatures within the optimal thermal range of this species. Crosses between warm- and cold-incubated gametes were compared using a fully-factorial design, with half of each clutch reared in cold temperatures and the other in warm temperatures. This allowed disentangling single-sex interaction effects when pre-fertilisation temperature of gametes mismatched embryonic conditions. Pre-fertilisation temperature influenced the age at hatch, and matching sperm and embryo temperatures resulted in earlier hatching. Warm incubation benefited eggs but harmed sperm, reducing the hatching success and, overall, gametic thermal plasticity did not enhance offspring fitness, indicating vulnerability to thermal changes. We highlight the sensitivity of male gametes to higher temperatures, and that gamete acclimation may not effectively buffer against deleterious effects of thermal fluctuations. From an applied angle, we propose the differential storage of male and female gametes as a tool to enhance sustainability within the hatcheries.</p>
Organizational effects of testosterone on the number of mating partners and reproductive success in females of a social rodent
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Baseline glucocorticoids alone do not predict reproductive success across years but in interaction with enzymatic antioxidants
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Data from: Reproductive senescence and mating tactic interact and conflict to drive reproductive success in a passerine
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Relative breeding timing and reproductive success of a resident montane bird species
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Position in the laying order has sex-specific consequences for reproductive success in adult black-headed gulls
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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)
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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.
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.